HEADER    SIGNALING PROTEIN                       15-JUL-15   5A8E              
TITLE     THERMOSTABILISED BETA1-ADRENOCEPTOR WITH RATIONALLY DESIGNED INVERSE  
TITLE    2 AGONIST 7-METHYLCYANOPINDOLOL BOUND                                  
COMPND    MOL_ID: 1;                                                            
COMPND   2 MOLECULE: BETA1 ADRENERGIC RECEPTOR;                                 
COMPND   3 CHAIN: A;                                                            
COMPND   4 ENGINEERED: YES;                                                     
COMPND   5 MUTATION: YES;                                                       
COMPND   6 OTHER_DETAILS: RESIDUES 3-32 AT THE N-TERMINUS AND RESIDUES 244-271  
COMPND   7 OF THE THIRD INTRACELLULAR LOOP WERE DELETED FROM THE CONSTRUCT. THE 
COMPND   8 CONSTRUCT WAS TRUNCATED AFTER RESIDUE 367 AND A HEXAHIS TAG ADDED.   
SOURCE    MOL_ID: 1;                                                            
SOURCE   2 ORGANISM_SCIENTIFIC: MELEAGRIS GALLOPAVO;                            
SOURCE   3 ORGANISM_COMMON: TURKEY;                                             
SOURCE   4 ORGANISM_TAXID: 9103;                                                
SOURCE   5 CELL: ERYTHROCYTE;                                                   
SOURCE   6 EXPRESSION_SYSTEM: TRICHOPLUSIA NI;                                  
SOURCE   7 EXPRESSION_SYSTEM_COMMON: CABBAGE LOOPER;                            
SOURCE   8 EXPRESSION_SYSTEM_TAXID: 7111;                                       
SOURCE   9 EXPRESSION_SYSTEM_CELL_LINE: HIGH FIVE;                              
SOURCE  10 EXPRESSION_SYSTEM_VECTOR_TYPE: BACULOVIRUS;                          
SOURCE  11 EXPRESSION_SYSTEM_PLASMID: PBACPAK8                                  
KEYWDS    SIGNALING PROTEIN, INVERSE AGONIST                                    
EXPDTA    X-RAY DIFFRACTION                                                     
AUTHOR    T.SATO,J.G.BAKER,T.WARNE,G.A.BROWN,M.CONGREVE,A.G.W.LESLIE,C.G.TATE   
REVDAT   4   03-APR-19 5A8E    1       SOURCE                                   
REVDAT   3   06-MAR-19 5A8E    1       REMARK                                   
REVDAT   2   11-NOV-15 5A8E    1       JRNL                                     
REVDAT   1   30-SEP-15 5A8E    0                                                
JRNL        AUTH   T.SATO,J.BAKER,T.WARNE,G.BROWN,A.LESLIE,M.CONGREVE,C.TATE    
JRNL        TITL   PHARMACOLOGICAL ANALYSIS AND STRUCTURE DETERMINATION OF      
JRNL        TITL 2 7-METHYLCYANOPINDOLOL-BOUND BETA1-ADRENERGIC RECEPTOR.       
JRNL        REF    MOL.PHARMACOL.                V.  88  1024 2015              
JRNL        REFN                   ISSN 0026-895X                               
JRNL        PMID   26385885                                                     
JRNL        DOI    10.1124/MOL.115.101030                                       
REMARK   2                                                                      
REMARK   2 RESOLUTION.    2.40 ANGSTROMS.                                       
REMARK   3                                                                      
REMARK   3 REFINEMENT.                                                          
REMARK   3   PROGRAM     : REFMAC 5.8.0107                                      
REMARK   3   AUTHORS     : MURSHUDOV,SKUBAK,LEBEDEV,PANNU,STEINER,              
REMARK   3               : NICHOLLS,WINN,LONG,VAGIN                             
REMARK   3                                                                      
REMARK   3    REFINEMENT TARGET : MAXIMUM LIKELIHOOD                            
REMARK   3                                                                      
REMARK   3  DATA USED IN REFINEMENT.                                            
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 2.40                           
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 37.79                          
REMARK   3   DATA CUTOFF            (SIGMA(F)) : NULL                           
REMARK   3   COMPLETENESS FOR RANGE        (%) : 98.0                           
REMARK   3   NUMBER OF REFLECTIONS             : 11942                          
REMARK   3                                                                      
REMARK   3  FIT TO DATA USED IN REFINEMENT.                                     
REMARK   3   CROSS-VALIDATION METHOD          : THROUGHOUT                      
REMARK   3   FREE R VALUE TEST SET SELECTION  : RANDOM                          
REMARK   3   R VALUE     (WORKING + TEST SET) : 0.218                           
REMARK   3   R VALUE            (WORKING SET) : 0.217                           
REMARK   3   FREE R VALUE                     : 0.248                           
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 4.800                           
REMARK   3   FREE R VALUE TEST SET COUNT      : 608                             
REMARK   3                                                                      
REMARK   3  FIT IN THE HIGHEST RESOLUTION BIN.                                  
REMARK   3   TOTAL NUMBER OF BINS USED           : 20                           
REMARK   3   BIN RESOLUTION RANGE HIGH       (A) : 2.40                         
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 2.46                         
REMARK   3   REFLECTION IN BIN     (WORKING SET) : 847                          
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 98.04                        
REMARK   3   BIN R VALUE           (WORKING SET) : 0.2940                       
REMARK   3   BIN FREE R VALUE SET COUNT          : 54                           
REMARK   3   BIN FREE R VALUE                    : 0.2850                       
REMARK   3                                                                      
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.                    
REMARK   3   PROTEIN ATOMS            : 2270                                    
REMARK   3   NUCLEIC ACID ATOMS       : 0                                       
REMARK   3   HETEROGEN ATOMS          : 137                                     
REMARK   3   SOLVENT ATOMS            : 26                                      
REMARK   3                                                                      
REMARK   3  B VALUES.                                                           
REMARK   3   FROM WILSON PLOT           (A**2) : NULL                           
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 39.35                          
REMARK   3   OVERALL ANISOTROPIC B VALUE.                                       
REMARK   3    B11 (A**2) : -0.03000                                             
REMARK   3    B22 (A**2) : 0.09000                                              
REMARK   3    B33 (A**2) : -0.06000                                             
REMARK   3    B12 (A**2) : 0.00000                                              
REMARK   3    B13 (A**2) : 0.00000                                              
REMARK   3    B23 (A**2) : 0.00000                                              
REMARK   3                                                                      
REMARK   3  ESTIMATED OVERALL COORDINATE ERROR.                                 
REMARK   3   ESU BASED ON R VALUE                            (A): 0.561         
REMARK   3   ESU BASED ON FREE R VALUE                       (A): 0.275         
REMARK   3   ESU BASED ON MAXIMUM LIKELIHOOD                 (A): 0.223         
REMARK   3   ESU FOR B VALUES BASED ON MAXIMUM LIKELIHOOD (A**2): 9.816         
REMARK   3                                                                      
REMARK   3 CORRELATION COEFFICIENTS.                                            
REMARK   3   CORRELATION COEFFICIENT FO-FC      : 0.922                         
REMARK   3   CORRELATION COEFFICIENT FO-FC FREE : 0.905                         
REMARK   3                                                                      
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES        COUNT    RMS    WEIGHT      
REMARK   3   BOND LENGTHS REFINED ATOMS        (A):  2461 ; 0.008 ; 0.020       
REMARK   3   BOND LENGTHS OTHERS               (A):  2510 ; 0.002 ; 0.020       
REMARK   3   BOND ANGLES REFINED ATOMS   (DEGREES):  3323 ; 1.290 ; 1.996       
REMARK   3   BOND ANGLES OTHERS          (DEGREES):  5740 ; 0.921 ; 3.000       
REMARK   3   TORSION ANGLES, PERIOD 1    (DEGREES):   285 ; 4.987 ; 5.000       
REMARK   3   TORSION ANGLES, PERIOD 2    (DEGREES):    86 ;36.951 ;21.860       
REMARK   3   TORSION ANGLES, PERIOD 3    (DEGREES):   396 ;13.654 ;15.000       
REMARK   3   TORSION ANGLES, PERIOD 4    (DEGREES):    17 ;15.620 ;15.000       
REMARK   3   CHIRAL-CENTER RESTRAINTS       (A**3):   387 ; 0.064 ; 0.200       
REMARK   3   GENERAL PLANES REFINED ATOMS      (A):  2600 ; 0.005 ; 0.020       
REMARK   3   GENERAL PLANES OTHERS             (A):   577 ; 0.001 ; 0.020       
REMARK   3   NON-BONDED CONTACTS REFINED ATOMS (A):  NULL ;  NULL ;  NULL       
REMARK   3   NON-BONDED CONTACTS OTHERS        (A):  NULL ;  NULL ;  NULL       
REMARK   3   NON-BONDED TORSION REFINED ATOMS  (A):  NULL ;  NULL ;  NULL       
REMARK   3   NON-BONDED TORSION OTHERS         (A):  NULL ;  NULL ;  NULL       
REMARK   3   H-BOND (X...Y) REFINED ATOMS      (A):  NULL ;  NULL ;  NULL       
REMARK   3   H-BOND (X...Y) OTHERS             (A):  NULL ;  NULL ;  NULL       
REMARK   3   POTENTIAL METAL-ION REFINED ATOMS (A):  NULL ;  NULL ;  NULL       
REMARK   3   POTENTIAL METAL-ION OTHERS        (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY VDW REFINED ATOMS        (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY VDW OTHERS               (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY H-BOND REFINED ATOMS     (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY H-BOND OTHERS            (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY METAL-ION REFINED ATOMS  (A):  NULL ;  NULL ;  NULL       
REMARK   3   SYMMETRY METAL-ION OTHERS         (A):  NULL ;  NULL ;  NULL       
REMARK   3                                                                      
REMARK   3  ISOTROPIC THERMAL FACTOR RESTRAINTS.     COUNT   RMS    WEIGHT      
REMARK   3   MAIN-CHAIN BOND REFINED ATOMS  (A**2):  1140 ; 1.370 ; 3.712       
REMARK   3   MAIN-CHAIN BOND OTHER ATOMS    (A**2):  1139 ; 1.370 ; 3.710       
REMARK   3   MAIN-CHAIN ANGLE REFINED ATOMS (A**2):  1422 ; 2.378 ; 5.555       
REMARK   3   MAIN-CHAIN ANGLE OTHER ATOMS   (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SIDE-CHAIN BOND REFINED ATOMS  (A**2):  1318 ; 1.555 ; 4.106       
REMARK   3   SIDE-CHAIN BOND OTHER ATOMS    (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SIDE-CHAIN ANGLE REFINED ATOMS (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SIDE-CHAIN ANGLE OTHER ATOMS   (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   LONG RANGE B REFINED ATOMS     (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   LONG RANGE B OTHER ATOMS       (A**2):  NULL ;  NULL ;  NULL       
REMARK   3                                                                      
REMARK   3 ANISOTROPIC THERMAL FACTOR RESTRAINTS.    COUNT   RMS   WEIGHT       
REMARK   3   RIGID-BOND RESTRAINTS          (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SPHERICITY; FREE ATOMS         (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SPHERICITY; BONDED ATOMS       (A**2):  NULL ;  NULL ;  NULL       
REMARK   3                                                                      
REMARK   3  NCS RESTRAINTS STATISTICS                                           
REMARK   3   NUMBER OF DIFFERENT NCS GROUPS : NULL                              
REMARK   3                                                                      
REMARK   3  TLS DETAILS                                                         
REMARK   3   NUMBER OF TLS GROUPS  : NULL                                       
REMARK   3                                                                      
REMARK   3  BULK SOLVENT MODELLING.                                             
REMARK   3   METHOD USED : MASK                                                 
REMARK   3   PARAMETERS FOR MASK CALCULATION                                    
REMARK   3   VDW PROBE RADIUS   : 1.20                                          
REMARK   3   ION PROBE RADIUS   : 0.80                                          
REMARK   3   SHRINKAGE RADIUS   : 0.80                                          
REMARK   3                                                                      
REMARK   3  OTHER REFINEMENT REMARKS: HYDROGENS HAVE BEEN ADDED IN THE RIDING   
REMARK   3  POSITIONS. U VALUES REFINED INDIVIDUALLY                            
REMARK   4                                                                      
REMARK   4 5A8E COMPLIES WITH FORMAT V. 3.30, 13-JUL-11                         
REMARK 100                                                                      
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBE ON 15-JUL-15.                  
REMARK 100 THE DEPOSITION ID IS D_1290063698.                                   
REMARK 200                                                                      
REMARK 200 EXPERIMENTAL DETAILS                                                 
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION                  
REMARK 200  DATE OF DATA COLLECTION        : NULL; NULL                         
REMARK 200  TEMPERATURE           (KELVIN) : 100; 100                           
REMARK 200  PH                             : 7                                  
REMARK 200  NUMBER OF CRYSTALS USED        : 4                                  
REMARK 200                                                                      
REMARK 200  SYNCHROTRON              (Y/N) : Y; Y                               
REMARK 200  RADIATION SOURCE               : ESRF; DIAMOND                      
REMARK 200  BEAMLINE                       : ID29; I24                          
REMARK 200  X-RAY GENERATOR MODEL          : NULL; NULL                         
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M; M                               
REMARK 200  WAVELENGTH OR RANGE        (A) : 0.8726; 0.969                      
REMARK 200  MONOCHROMATOR                  : NULL; NULL                         
REMARK 200  OPTICS                         : NULL; NULL                         
REMARK 200                                                                      
REMARK 200  DETECTOR TYPE                  : PIXEL; CCD                         
REMARK 200  DETECTOR MANUFACTURER          : PILATUS; ADSC CCD                  
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : MOSFLM                             
REMARK 200  DATA SCALING SOFTWARE          : AIMLESS                            
REMARK 200                                                                      
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 12526                              
REMARK 200  RESOLUTION RANGE HIGH      (A) : 2.400                              
REMARK 200  RESOLUTION RANGE LOW       (A) : 37.800                             
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : 2.000                              
REMARK 200                                                                      
REMARK 200 OVERALL.                                                             
REMARK 200  COMPLETENESS FOR RANGE     (%) : 98.4                               
REMARK 200  DATA REDUNDANCY                : 4.800                              
REMARK 200  R MERGE                    (I) : 0.16000                            
REMARK 200  R SYM                      (I) : NULL                               
REMARK 200  <I/SIGMA(I)> FOR THE DATA SET  : 8.2000                             
REMARK 200                                                                      
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.                                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 2.40                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 2.53                     
REMARK 200  COMPLETENESS FOR SHELL     (%) : 98.3                               
REMARK 200  DATA REDUNDANCY IN SHELL       : 4.90                               
REMARK 200  R MERGE FOR SHELL          (I) : 0.70000                            
REMARK 200  R SYM FOR SHELL            (I) : NULL                               
REMARK 200  <I/SIGMA(I)> FOR SHELL         : 1.900                              
REMARK 200                                                                      
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH; SINGLE WAVELENGTH           
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MIR                          
REMARK 200 SOFTWARE USED: PHASER                                                
REMARK 200 STARTING MODEL: PDB ENTRY 4BVN                                       
REMARK 200                                                                      
REMARK 200 REMARK: NONE                                                         
REMARK 280                                                                      
REMARK 280 CRYSTAL                                                              
REMARK 280 SOLVENT CONTENT, VS   (%): 43.40                                     
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.17                     
REMARK 280                                                                      
REMARK 280 CRYSTALLIZATION CONDITIONS: 25% PEG600, 0.1M ADA PH7.0, LIPIDIC      
REMARK 280  CUBIC PHASE (LCP), TEMPERATURE 293K                                 
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY                                            
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 21 2 21                        
REMARK 290                                                                      
REMARK 290      SYMOP   SYMMETRY                                                
REMARK 290     NNNMMM   OPERATOR                                                
REMARK 290       1555   X,Y,Z                                                   
REMARK 290       2555   -X,Y,-Z                                                 
REMARK 290       3555   X+1/2,-Y,-Z+1/2                                         
REMARK 290       4555   -X+1/2,-Y,Z+1/2                                         
REMARK 290                                                                      
REMARK 290     WHERE NNN -> OPERATOR NUMBER                                     
REMARK 290           MMM -> TRANSLATION VECTOR                                  
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY TRANSFORMATIONS                            
REMARK 290 THE FOLLOWING TRANSFORMATIONS OPERATE ON THE ATOM/HETATM             
REMARK 290 RECORDS IN THIS ENTRY TO PRODUCE CRYSTALLOGRAPHICALLY                
REMARK 290 RELATED MOLECULES.                                                   
REMARK 290   SMTRY1   1  1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   1  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   1  0.000000  0.000000  1.000000        0.00000            
REMARK 290   SMTRY1   2 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   2  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   2  0.000000  0.000000 -1.000000        0.00000            
REMARK 290   SMTRY1   3  1.000000  0.000000  0.000000       26.50950            
REMARK 290   SMTRY2   3  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   3  0.000000  0.000000 -1.000000       47.78050            
REMARK 290   SMTRY1   4 -1.000000  0.000000  0.000000       26.50950            
REMARK 290   SMTRY2   4  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   4  0.000000  0.000000  1.000000       47.78050            
REMARK 290                                                                      
REMARK 290 REMARK: NULL                                                         
REMARK 300                                                                      
REMARK 300 BIOMOLECULE: 1                                                       
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM                
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN                  
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON               
REMARK 300 BURIED SURFACE AREA.                                                 
REMARK 350                                                                      
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN           
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE                
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS          
REMARK 350 GIVEN BELOW.  BOTH NON-CRYSTALLOGRAPHIC AND                          
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.                               
REMARK 350                                                                      
REMARK 350 BIOMOLECULE: 1                                                       
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: MONOMERIC                         
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: MONOMERIC                  
REMARK 350 SOFTWARE USED: PISA                                                  
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A                                     
REMARK 350   BIOMT1   1  1.000000  0.000000  0.000000        0.00000            
REMARK 350   BIOMT2   1  0.000000  1.000000  0.000000        0.00000            
REMARK 350   BIOMT3   1  0.000000  0.000000  1.000000        0.00000            
REMARK 465                                                                      
REMARK 465 MISSING RESIDUES                                                     
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE                       
REMARK 465 EXPERIMENT. (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN               
REMARK 465 IDENTIFIER; SSSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)                
REMARK 465                                                                      
REMARK 465   M RES C SSSEQI                                                     
REMARK 465     MET A    31                                                      
REMARK 465     GLY A    32                                                      
REMARK 465     ALA A    33                                                      
REMARK 465     GLU A    34                                                      
REMARK 465     LEU A    35                                                      
REMARK 465     ILE A   241                                                      
REMARK 465     ASP A   242                                                      
REMARK 465     ARG A   243                                                      
REMARK 465     ALA A   244                                                      
REMARK 465     SER A   245                                                      
REMARK 465     LYS A   246                                                      
REMARK 465     ARG A   355                                                      
REMARK 465     LEU A   356                                                      
REMARK 465     LEU A   357                                                      
REMARK 465     ALA A   358                                                      
REMARK 465     PHE A   359                                                      
REMARK 465     PRO A   360                                                      
REMARK 465     ARG A   361                                                      
REMARK 465     LYS A   362                                                      
REMARK 465     ALA A   363                                                      
REMARK 465     ASP A   364                                                      
REMARK 465     ARG A   365                                                      
REMARK 465     ARG A   366                                                      
REMARK 465     LEU A   367                                                      
REMARK 465     HIS A   368                                                      
REMARK 465     HIS A   369                                                      
REMARK 465     HIS A   370                                                      
REMARK 465     HIS A   371                                                      
REMARK 465     HIS A   372                                                      
REMARK 465     HIS A   373                                                      
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: CLOSE CONTACTS                                             
REMARK 500                                                                      
REMARK 500 THE FOLLOWING ATOMS THAT ARE RELATED BY CRYSTALLOGRAPHIC             
REMARK 500 SYMMETRY ARE IN CLOSE CONTACT.  AN ATOM LOCATED WITHIN 0.15          
REMARK 500 ANGSTROMS OF A SYMMETRY RELATED ATOM IS ASSUMED TO BE ON A           
REMARK 500 SPECIAL POSITION AND IS, THEREFORE, LISTED IN REMARK 375             
REMARK 500 INSTEAD OF REMARK 500.  ATOMS WITH NON-BLANK ALTERNATE               
REMARK 500 LOCATION INDICATORS ARE NOT INCLUDED IN THE CALCULATIONS.            
REMARK 500                                                                      
REMARK 500 DISTANCE CUTOFF:                                                     
REMARK 500 2.2 ANGSTROMS FOR CONTACTS NOT INVOLVING HYDROGEN ATOMS              
REMARK 500 1.6 ANGSTROMS FOR CONTACTS INVOLVING HYDROGEN ATOMS                  
REMARK 500                                                                      
REMARK 500  ATM1  RES C  SSEQI   ATM2  RES C  SSEQI  SSYMOP   DISTANCE          
REMARK 500   OG   SER A   145     OG   SER A   145     2655     1.82            
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: TORSION ANGLES                                             
REMARK 500                                                                      
REMARK 500 TORSION ANGLES OUTSIDE THE EXPECTED RAMACHANDRAN REGIONS:            
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;               
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).                             
REMARK 500                                                                      
REMARK 500 STANDARD TABLE:                                                      
REMARK 500 FORMAT:(10X,I3,1X,A3,1X,A1,I4,A1,4X,F7.2,3X,F7.2)                    
REMARK 500                                                                      
REMARK 500 EXPECTED VALUES: GJ KLEYWEGT AND TA JONES (1996). PHI/PSI-           
REMARK 500 CHOLOGY: RAMACHANDRAN REVISITED. STRUCTURE 4, 1395 - 1400            
REMARK 500                                                                      
REMARK 500  M RES CSSEQI        PSI       PHI                                   
REMARK 500    PHE A 216      -64.47   -139.87                                   
REMARK 500    THR A 277      138.51    -37.27                                   
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 610                                                                      
REMARK 610 MISSING HETEROATOM                                                   
REMARK 610 THE FOLLOWING RESIDUES HAVE MISSING ATOMS (M=MODEL NUMBER;           
REMARK 610 RES=RESIDUE NAME; C=CHAIN IDENTIFIER; SSEQ=SEQUENCE NUMBER;          
REMARK 610 I=INSERTION CODE):                                                   
REMARK 610   M RES C SSEQI                                                      
REMARK 610     OLC A 2001                                                       
REMARK 610     OLC A 2003                                                       
REMARK 610     OLC A 2004                                                       
REMARK 620                                                                      
REMARK 620 METAL COORDINATION                                                   
REMARK 620 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;               
REMARK 620 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE):                             
REMARK 620                                                                      
REMARK 620 COORDINATION ANGLES FOR:  M RES CSSEQI METAL                         
REMARK 620                              NA A 401  NA                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 HOH A3014   O                                                      
REMARK 620 2 HOH A3015   O    96.5                                              
REMARK 620 3 ASP A 195   O   163.7  82.3                                        
REMARK 620 4 HOH A3009   O   101.4  79.7  94.4                                  
REMARK 620 5 CYS A 192   O    95.7 109.0  69.6 159.9                            
REMARK 620 6 CYS A 198   O    99.8 151.3  88.3  74.0  92.8                      
REMARK 620 N                    1     2     3     4     5                       
REMARK 620                                                                      
REMARK 620 COORDINATION ANGLES FOR:  M RES CSSEQI METAL                         
REMARK 620                              NA A 402  NA                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 ASP A  87   OD1                                                    
REMARK 620 2 HOH A3003   O    86.8                                              
REMARK 620 3 HOH A3004   O    65.1 150.4                                        
REMARK 620 4 HOH A3022   O   101.1 113.2  82.9                                  
REMARK 620 5 SER A 128   OG  130.7  96.9  94.8 121.5                            
REMARK 620 N                    1     2     3     4                             
REMARK 800                                                                      
REMARK 800 SITE                                                                 
REMARK 800 SITE_IDENTIFIER: AC1                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE NA A 401                  
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC2                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE NA A 402                  
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC3                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE XTK A 501                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC4                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE MHA A 801                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC5                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OLC A 2001                
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC6                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OLC A 2002                
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC7                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OLC A 2003                
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC8                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OLC A 2004                
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC9                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OLC A 2005                
REMARK 999                                                                      
REMARK 999 SEQUENCE                                                             
REMARK 999 THE FOLLOWING MUTATIONS WERE MADE TO IMPROVE                         
REMARK 999 THERMOSTABILITY R68S,M90V,I129V,Y227A,A282L,F327A,F338M,             
REMARK 999 Y343L. THE FOLLOWING MUTATIONS WERE MADE TO IMPROVE                  
REMARK 999 EXPRESSION AND HELP CRYSTALLIZATION C116L, E130W,C358A.              
DBREF  5A8E A   33   368  UNP    P07700   ADRB1_MELGA     33    368             
SEQADV 5A8E MET A   31  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E GLY A   32  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E HIS A  369  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E HIS A  370  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E HIS A  371  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E HIS A  372  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E HIS A  373  UNP  P07700              EXPRESSION TAG                 
SEQADV 5A8E SER A   68  UNP  P07700    ARG    68 ENGINEERED MUTATION            
SEQADV 5A8E VAL A   90  UNP  P07700    MET    90 ENGINEERED MUTATION            
SEQADV 5A8E LEU A  116  UNP  P07700    CYS   116 ENGINEERED MUTATION            
SEQADV 5A8E VAL A  129  UNP  P07700    ILE   129 ENGINEERED MUTATION            
SEQADV 5A8E TRP A  130  UNP  P07700    GLU   130 ENGINEERED MUTATION            
SEQADV 5A8E ALA A  227  UNP  P07700    TYR   227 ENGINEERED MUTATION            
SEQADV 5A8E LEU A  282  UNP  P07700    ALA   282 ENGINEERED MUTATION            
SEQADV 5A8E ALA A  327  UNP  P07700    PHE   327 ENGINEERED MUTATION            
SEQADV 5A8E MET A  338  UNP  P07700    PHE   338 ENGINEERED MUTATION            
SEQADV 5A8E LEU A  343  UNP  P07700    TYR   343 ENGINEERED MUTATION            
SEQADV 5A8E ALA A  358  UNP  P07700    CYS   358 ENGINEERED MUTATION            
SEQRES   1 A  315  MET GLY ALA GLU LEU LEU SER GLN GLN TRP GLU ALA GLY          
SEQRES   2 A  315  MET SER LEU LEU MET ALA LEU VAL VAL LEU LEU ILE VAL          
SEQRES   3 A  315  ALA GLY ASN VAL LEU VAL ILE ALA ALA ILE GLY SER THR          
SEQRES   4 A  315  GLN ARG LEU GLN THR LEU THR ASN LEU PHE ILE THR SER          
SEQRES   5 A  315  LEU ALA CYS ALA ASP LEU VAL VAL GLY LEU LEU VAL VAL          
SEQRES   6 A  315  PRO PHE GLY ALA THR LEU VAL VAL ARG GLY THR TRP LEU          
SEQRES   7 A  315  TRP GLY SER PHE LEU CYS GLU LEU TRP THR SER LEU ASP          
SEQRES   8 A  315  VAL LEU CYS VAL THR ALA SER VAL TRP THR LEU CYS VAL          
SEQRES   9 A  315  ILE ALA ILE ASP ARG TYR LEU ALA ILE THR SER PRO PHE          
SEQRES  10 A  315  ARG TYR GLN SER LEU MET THR ARG ALA ARG ALA LYS VAL          
SEQRES  11 A  315  ILE ILE CYS THR VAL TRP ALA ILE SER ALA LEU VAL SER          
SEQRES  12 A  315  PHE LEU PRO ILE MET MET HIS TRP TRP ARG ASP GLU ASP          
SEQRES  13 A  315  PRO GLN ALA LEU LYS CYS TYR GLN ASP PRO GLY CYS CYS          
SEQRES  14 A  315  ASP PHE VAL THR ASN ARG ALA TYR ALA ILE ALA SER SER          
SEQRES  15 A  315  ILE ILE SER PHE TYR ILE PRO LEU LEU ILE MET ILE PHE          
SEQRES  16 A  315  VAL ALA LEU ARG VAL TYR ARG GLU ALA LYS GLU GLN ILE          
SEQRES  17 A  315  ARG LYS ILE ASP ARG ALA SER LYS ARG LYS THR SER ARG          
SEQRES  18 A  315  VAL MET LEU MET ARG GLU HIS LYS ALA LEU LYS THR LEU          
SEQRES  19 A  315  GLY ILE ILE MET GLY VAL PHE THR LEU CYS TRP LEU PRO          
SEQRES  20 A  315  PHE PHE LEU VAL ASN ILE VAL ASN VAL PHE ASN ARG ASP          
SEQRES  21 A  315  LEU VAL PRO ASP TRP LEU PHE VAL ALA PHE ASN TRP LEU          
SEQRES  22 A  315  GLY TYR ALA ASN SER ALA MET ASN PRO ILE ILE LEU CYS          
SEQRES  23 A  315  ARG SER PRO ASP PHE ARG LYS ALA PHE LYS ARG LEU LEU          
SEQRES  24 A  315  ALA PHE PRO ARG LYS ALA ASP ARG ARG LEU HIS HIS HIS          
SEQRES  25 A  315  HIS HIS HIS                                                  
HET     NA  A 401       1                                                       
HET     NA  A 402       1                                                       
HET    XTK  A 501      22                                                       
HET    MHA  A 801      13                                                       
HET    OLC  A2001      16                                                       
HET    OLC  A2002      25                                                       
HET    OLC  A2003      13                                                       
HET    OLC  A2004      21                                                       
HET    OLC  A2005      25                                                       
HETNAM      NA SODIUM ION                                                       
HETNAM     XTK 4-[(2S)-3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY]-7-METHYL-          
HETNAM   2 XTK  1H-INDOLE-2-CARBONITRILE                                        
HETNAM     MHA (CARBAMOYLMETHYL-CARBOXYMETHYL-AMINO)-ACETIC ACID                
HETNAM     OLC (2R)-2,3-DIHYDROXYPROPYL (9Z)-OCTADEC-9-ENOATE                   
HETSYN     MHA N-(2-ACETAMIDO)IMINODIACETIC ACID                                
HETSYN     OLC 1-OLEOYL-R-GLYCEROL                                              
FORMUL   2   NA    2(NA 1+)                                                     
FORMUL   4  XTK    C17 H23 N3 O2                                                
FORMUL   5  MHA    C6 H10 N2 O5                                                 
FORMUL   6  OLC    5(C21 H40 O4)                                                
FORMUL  11  HOH   *26(H2 O)                                                     
HELIX    1   1 LEU A   36  SER A   68  1                                  33    
HELIX    2   2 THR A   74  LEU A   93  1                                  20    
HELIX    3   3 LEU A   93  GLY A  105  1                                  13    
HELIX    4   4 TRP A  109  SER A  145  1                                  37    
HELIX    5   5 SER A  145  MET A  153  1                                   9    
HELIX    6   6 THR A  154  MET A  179  1                                  26    
HELIX    7   7 ASP A  186  ASP A  195  1                                  10    
HELIX    8   8 ASN A  204  PHE A  216  1                                  13    
HELIX    9   9 PHE A  216  LYS A  240  1                                  25    
HELIX   10  10 SER A  278  ASN A  316  1                                  39    
HELIX   11  11 ARG A  317  VAL A  320  5                                   4    
HELIX   12  12 PRO A  321  ARG A  345  1                                  25    
HELIX   13  13 SER A  346  LYS A  354  1                                   9    
SSBOND   1 CYS A  114    CYS A  199                          1555   1555  2.04  
SSBOND   2 CYS A  192    CYS A  198                          1555   1555  2.06  
LINK        NA    NA A 401                 O   HOH A3014     1555   1555  2.30  
LINK        NA    NA A 401                 O   HOH A3015     1555   1555  2.33  
LINK        NA    NA A 401                 O   ASP A 195     1555   1555  2.52  
LINK        NA    NA A 401                 O   HOH A3009     1555   1555  2.69  
LINK        NA    NA A 401                 O   CYS A 192     1555   1555  2.56  
LINK        NA    NA A 401                 O   CYS A 198     1555   1555  2.31  
LINK        NA    NA A 402                 OD1 ASP A  87     1555   1555  2.60  
LINK        NA    NA A 402                 O   HOH A3003     1555   1555  2.13  
LINK        NA    NA A 402                 O   HOH A3004     1555   1555  2.57  
LINK        NA    NA A 402                 O   HOH A3022     1555   1555  2.32  
LINK        NA    NA A 402                 OG  SER A 128     1555   1555  2.46  
SITE     1 AC1  6 CYS A 192  ASP A 195  CYS A 198  HOH A3009                    
SITE     2 AC1  6 HOH A3014  HOH A3015                                          
SITE     1 AC2  5 ASP A  87  SER A 128  HOH A3003  HOH A3004                    
SITE     2 AC2  5 HOH A3022                                                     
SITE     1 AC3 13 TRP A 117  ASP A 121  VAL A 122  THR A 203                    
SITE     2 AC3 13 ALA A 208  SER A 211  SER A 215  TRP A 303                    
SITE     3 AC3 13 PHE A 306  PHE A 307  ASN A 310  ASN A 329                    
SITE     4 AC3 13 TYR A 333                                                     
SITE     1 AC4 10 GLY A 110  SER A 111  PRO A 196  LYS A 287                    
SITE     2 AC4 10 LYS A 290  THR A 291  ARG A 345  SER A 346                    
SITE     3 AC4 10 HOH A3008  HOH A3026                                          
SITE     1 AC5  7 ALA A 227  ILE A 238  ARG A 239  HIS A 286                    
SITE     2 AC5  7 LEU A 289  GLY A 293  OLC A2002                               
SITE     1 AC6  8 TRP A 107  LEU A 108  ASP A 195  GLY A 197                    
SITE     2 AC6  8 LYS A 287  LYS A 290  GLY A 293  OLC A2001                    
SITE     1 AC7  1 TYR A 140                                                     
SITE     1 AC8  9 GLN A  73  THR A  74  LEU A  75  THR A  76                    
SITE     2 AC8  9 ARG A 139  ILE A 143  ARG A 155  GLU A 285                    
SITE     3 AC8  9 ALA A 288                                                     
SITE     1 AC9  6 TRP A 181  ASP A 184  ASN A 204  ARG A 205                    
SITE     2 AC9  6 LYS A 276  PHE A 315                                          
CRYST1   53.019   61.777   95.561  90.00  90.00  90.00 P 21 2 21     4          
ORIGX1      1.000000  0.000000  0.000000        0.00000                         
ORIGX2      0.000000  1.000000  0.000000        0.00000                         
ORIGX3      0.000000  0.000000  1.000000        0.00000                         
SCALE1      0.018861  0.000000  0.000000        0.00000                         
SCALE2      0.000000  0.016187  0.000000        0.00000                         
SCALE3      0.000000  0.000000  0.010465        0.00000                         
ATOM      1  N   LEU A  36      28.465  41.894  43.339  1.00 95.49           N  
ATOM      2  CA  LEU A  36      29.415  42.780  42.592  1.00 96.34           C  
ATOM      3  C   LEU A  36      28.821  43.333  41.295  1.00 98.32           C  
ATOM      4  O   LEU A  36      29.086  44.481  40.934  1.00 98.08           O  
ATOM      5  CB  LEU A  36      30.721  42.036  42.290  1.00 95.56           C  
ATOM      6  CG  LEU A  36      31.860  42.835  41.648  1.00 93.96           C  
ATOM      7  CD1 LEU A  36      32.237  44.039  42.502  1.00 93.87           C  
ATOM      8  CD2 LEU A  36      33.059  41.927  41.420  1.00 92.35           C  
ATOM      9  N   SER A  37      28.048  42.506  40.591  1.00101.01           N  
ATOM     10  CA  SER A  37      27.246  42.962  39.447  1.00103.08           C  
ATOM     11  C   SER A  37      26.144  43.941  39.879  1.00106.54           C  
ATOM     12  O   SER A  37      25.751  44.816  39.102  1.00110.44           O  
ATOM     13  CB  SER A  37      26.626  41.768  38.715  1.00102.13           C  
ATOM     14  OG  SER A  37      25.752  41.043  39.563  1.00100.54           O  
ATOM     15  N   GLN A  38      25.648  43.776  41.108  1.00106.92           N  
ATOM     16  CA  GLN A  38      24.687  44.704  41.718  1.00104.39           C  
ATOM     17  C   GLN A  38      25.318  46.065  42.046  1.00100.89           C  
ATOM     18  O   GLN A  38      24.659  47.098  41.910  1.00100.30           O  
ATOM     19  CB  GLN A  38      24.085  44.081  42.987  1.00105.47           C  
ATOM     20  CG  GLN A  38      22.888  44.818  43.583  1.00107.19           C  
ATOM     21  CD  GLN A  38      21.582  44.588  42.832  1.00107.23           C  
ATOM     22  OE1 GLN A  38      21.571  44.151  41.678  1.00105.69           O  
ATOM     23  NE2 GLN A  38      20.465  44.888  43.492  1.00106.18           N  
ATOM     24  N   GLN A  39      26.575  46.060  42.492  1.00 97.65           N  
ATOM     25  CA  GLN A  39      27.335  47.304  42.715  1.00 96.16           C  
ATOM     26  C   GLN A  39      27.554  48.091  41.417  1.00 91.92           C  
ATOM     27  O   GLN A  39      27.482  49.323  41.417  1.00 95.05           O  
ATOM     28  CB  GLN A  39      28.690  47.015  43.388  1.00 97.89           C  
ATOM     29  CG  GLN A  39      28.608  46.772  44.892  1.00 98.12           C  
ATOM     30  CD  GLN A  39      28.329  48.034  45.699  1.00 99.98           C  
ATOM     31  OE1 GLN A  39      28.327  49.146  45.168  1.00101.20           O  
ATOM     32  NE2 GLN A  39      28.091  47.862  46.997  1.00102.41           N  
ATOM     33  N   TRP A  40      27.821  47.374  40.325  1.00 84.81           N  
ATOM     34  CA  TRP A  40      27.959  47.980  38.997  1.00 80.04           C  
ATOM     35  C   TRP A  40      26.609  48.458  38.442  1.00 79.29           C  
ATOM     36  O   TRP A  40      26.532  49.539  37.859  1.00 77.91           O  
ATOM     37  CB  TRP A  40      28.602  46.985  38.030  1.00 77.44           C  
ATOM     38  CG  TRP A  40      29.028  47.584  36.733  1.00 74.53           C  
ATOM     39  CD1 TRP A  40      30.121  48.369  36.516  1.00 75.76           C  
ATOM     40  CD2 TRP A  40      28.381  47.433  35.466  1.00 72.52           C  
ATOM     41  NE1 TRP A  40      30.193  48.725  35.191  1.00 75.39           N  
ATOM     42  CE2 TRP A  40      29.138  48.164  34.522  1.00 73.45           C  
ATOM     43  CE3 TRP A  40      27.232  46.755  35.035  1.00 70.42           C  
ATOM     44  CZ2 TRP A  40      28.785  48.235  33.168  1.00 72.88           C  
ATOM     45  CZ3 TRP A  40      26.882  46.824  33.689  1.00 70.07           C  
ATOM     46  CH2 TRP A  40      27.657  47.562  32.772  1.00 71.32           C  
ATOM     47  N   GLU A  41      25.563  47.646  38.614  1.00 77.53           N  
ATOM     48  CA  GLU A  41      24.189  48.040  38.249  1.00 77.61           C  
ATOM     49  C   GLU A  41      23.729  49.294  38.992  1.00 76.92           C  
ATOM     50  O   GLU A  41      23.213  50.226  38.378  1.00 79.25           O  
ATOM     51  CB  GLU A  41      23.178  46.911  38.519  1.00 78.13           C  
ATOM     52  CG  GLU A  41      22.967  45.943  37.362  1.00 79.52           C  
ATOM     53  CD  GLU A  41      21.689  45.129  37.502  1.00 80.73           C  
ATOM     54  OE1 GLU A  41      21.292  44.818  38.646  1.00 82.13           O  
ATOM     55  OE2 GLU A  41      21.079  44.795  36.465  1.00 79.02           O  
ATOM     56  N   ALA A  42      23.908  49.293  40.312  1.00 74.80           N  
ATOM     57  CA  ALA A  42      23.539  50.430  41.162  1.00 72.88           C  
ATOM     58  C   ALA A  42      24.417  51.651  40.895  1.00 71.01           C  
ATOM     59  O   ALA A  42      23.925  52.781  40.914  1.00 68.72           O  
ATOM     60  CB  ALA A  42      23.622  50.043  42.631  1.00 72.21           C  
ATOM     61  N   GLY A  43      25.708  51.410  40.658  1.00 70.42           N  
ATOM     62  CA  GLY A  43      26.675  52.464  40.352  1.00 69.59           C  
ATOM     63  C   GLY A  43      26.413  53.139  39.021  1.00 68.87           C  
ATOM     64  O   GLY A  43      26.407  54.369  38.938  1.00 68.15           O  
ATOM     65  N   MET A  44      26.192  52.332  37.982  1.00 68.75           N  
ATOM     66  CA  MET A  44      25.886  52.850  36.644  1.00 68.25           C  
ATOM     67  C   MET A  44      24.505  53.511  36.589  1.00 65.63           C  
ATOM     68  O   MET A  44      24.368  54.578  36.000  1.00 67.05           O  
ATOM     69  CB  MET A  44      26.002  51.754  35.575  1.00 70.30           C  
ATOM     70  CG  MET A  44      27.432  51.347  35.233  1.00 72.50           C  
ATOM     71  SD  MET A  44      28.340  52.635  34.352  1.00 76.15           S  
ATOM     72  CE  MET A  44      29.555  51.689  33.437  1.00 77.41           C  
ATOM     73  N   SER A  45      23.500  52.893  37.213  1.00 60.80           N  
ATOM     74  CA  SER A  45      22.155  53.491  37.337  1.00 59.80           C  
ATOM     75  C   SER A  45      22.177  54.954  37.791  1.00 59.01           C  
ATOM     76  O   SER A  45      21.507  55.799  37.194  1.00 59.92           O  
ATOM     77  CB  SER A  45      21.284  52.689  38.315  1.00 59.81           C  
ATOM     78  OG  SER A  45      20.833  51.476  37.738  1.00 60.22           O  
ATOM     79  N   LEU A  46      22.947  55.235  38.841  1.00 57.60           N  
ATOM     80  CA  LEU A  46      23.053  56.586  39.407  1.00 57.57           C  
ATOM     81  C   LEU A  46      23.804  57.538  38.478  1.00 55.82           C  
ATOM     82  O   LEU A  46      23.376  58.676  38.291  1.00 57.37           O  
ATOM     83  CB  LEU A  46      23.734  56.545  40.785  1.00 59.48           C  
ATOM     84  CG  LEU A  46      23.967  57.868  41.531  1.00 60.40           C  
ATOM     85  CD1 LEU A  46      22.669  58.634  41.750  1.00 60.27           C  
ATOM     86  CD2 LEU A  46      24.662  57.601  42.856  1.00 60.58           C  
ATOM     87  N   LEU A  47      24.923  57.072  37.920  1.00 53.55           N  
ATOM     88  CA  LEU A  47      25.688  57.830  36.912  1.00 53.05           C  
ATOM     89  C   LEU A  47      24.842  58.201  35.677  1.00 51.13           C  
ATOM     90  O   LEU A  47      24.995  59.291  35.124  1.00 48.78           O  
ATOM     91  CB  LEU A  47      26.943  57.045  36.482  1.00 53.61           C  
ATOM     92  CG  LEU A  47      27.733  57.523  35.252  1.00 55.98           C  
ATOM     93  CD1 LEU A  47      28.274  58.936  35.431  1.00 56.88           C  
ATOM     94  CD2 LEU A  47      28.869  56.558  34.946  1.00 56.75           C  
ATOM     95  N   MET A  48      23.963  57.293  35.253  1.00 49.36           N  
ATOM     96  CA  MET A  48      23.076  57.550  34.115  1.00 48.89           C  
ATOM     97  C   MET A  48      21.985  58.566  34.465  1.00 47.54           C  
ATOM     98  O   MET A  48      21.639  59.403  33.635  1.00 48.58           O  
ATOM     99  CB  MET A  48      22.442  56.251  33.608  1.00 49.38           C  
ATOM    100  CG  MET A  48      23.432  55.218  33.083  1.00 50.41           C  
ATOM    101  SD  MET A  48      24.322  55.700  31.599  1.00 51.09           S  
ATOM    102  CE  MET A  48      25.085  54.139  31.159  1.00 51.53           C  
ATOM    103  N   ALA A  49      21.449  58.490  35.683  1.00 45.83           N  
ATOM    104  CA  ALA A  49      20.487  59.482  36.175  1.00 44.76           C  
ATOM    105  C   ALA A  49      21.071  60.898  36.155  1.00 44.71           C  
ATOM    106  O   ALA A  49      20.396  61.834  35.732  1.00 44.69           O  
ATOM    107  CB  ALA A  49      20.028  59.124  37.579  1.00 44.90           C  
ATOM    108  N   LEU A  50      22.324  61.039  36.593  1.00 44.83           N  
ATOM    109  CA  LEU A  50      23.034  62.326  36.563  1.00 44.94           C  
ATOM    110  C   LEU A  50      23.302  62.836  35.141  1.00 42.75           C  
ATOM    111  O   LEU A  50      23.168  64.034  34.880  1.00 42.89           O  
ATOM    112  CB  LEU A  50      24.358  62.247  37.344  1.00 46.73           C  
ATOM    113  CG  LEU A  50      24.294  61.962  38.854  1.00 49.21           C  
ATOM    114  CD1 LEU A  50      25.664  62.177  39.485  1.00 49.05           C  
ATOM    115  CD2 LEU A  50      23.244  62.815  39.563  1.00 50.46           C  
ATOM    116  N   VAL A  51      23.677  61.937  34.233  1.00 40.34           N  
ATOM    117  CA  VAL A  51      23.817  62.288  32.808  1.00 39.36           C  
ATOM    118  C   VAL A  51      22.478  62.778  32.225  1.00 37.07           C  
ATOM    119  O   VAL A  51      22.434  63.815  31.556  1.00 33.30           O  
ATOM    120  CB  VAL A  51      24.385  61.109  31.982  1.00 39.68           C  
ATOM    121  CG1 VAL A  51      24.245  61.351  30.483  1.00 40.02           C  
ATOM    122  CG2 VAL A  51      25.851  60.881  32.332  1.00 40.24           C  
ATOM    123  N   VAL A  52      21.402  62.037  32.495  1.00 36.53           N  
ATOM    124  CA  VAL A  52      20.051  62.427  32.059  1.00 38.00           C  
ATOM    125  C   VAL A  52      19.694  63.816  32.605  1.00 38.83           C  
ATOM    126  O   VAL A  52      19.254  64.688  31.848  1.00 39.37           O  
ATOM    127  CB  VAL A  52      18.967  61.398  32.485  1.00 37.46           C  
ATOM    128  CG1 VAL A  52      17.556  61.933  32.236  1.00 37.03           C  
ATOM    129  CG2 VAL A  52      19.146  60.078  31.744  1.00 37.63           C  
ATOM    130  N   LEU A  53      19.897  64.012  33.909  1.00 39.01           N  
ATOM    131  CA  LEU A  53      19.589  65.288  34.563  1.00 39.99           C  
ATOM    132  C   LEU A  53      20.388  66.453  33.973  1.00 38.31           C  
ATOM    133  O   LEU A  53      19.840  67.528  33.752  1.00 40.00           O  
ATOM    134  CB  LEU A  53      19.841  65.200  36.076  1.00 42.05           C  
ATOM    135  CG  LEU A  53      19.514  66.445  36.922  1.00 42.70           C  
ATOM    136  CD1 LEU A  53      18.035  66.773  36.844  1.00 42.49           C  
ATOM    137  CD2 LEU A  53      19.948  66.256  38.370  1.00 43.29           C  
ATOM    138  N   LEU A  54      21.676  66.235  33.733  1.00 36.01           N  
ATOM    139  CA  LEU A  54      22.544  67.254  33.135  1.00 34.44           C  
ATOM    140  C   LEU A  54      22.109  67.608  31.715  1.00 31.85           C  
ATOM    141  O   LEU A  54      22.004  68.782  31.374  1.00 30.69           O  
ATOM    142  CB  LEU A  54      23.998  66.764  33.126  1.00 35.74           C  
ATOM    143  CG  LEU A  54      25.089  67.719  32.630  1.00 36.68           C  
ATOM    144  CD1 LEU A  54      25.260  68.886  33.593  1.00 36.56           C  
ATOM    145  CD2 LEU A  54      26.403  66.972  32.451  1.00 36.59           C  
ATOM    146  N   ILE A  55      21.865  66.592  30.891  1.00 31.03           N  
ATOM    147  CA  ILE A  55      21.436  66.808  29.504  1.00 30.36           C  
ATOM    148  C   ILE A  55      20.076  67.500  29.469  1.00 30.07           C  
ATOM    149  O   ILE A  55      19.905  68.486  28.754  1.00 29.60           O  
ATOM    150  CB  ILE A  55      21.374  65.484  28.690  1.00 30.14           C  
ATOM    151  CG1 ILE A  55      22.787  64.925  28.470  1.00 29.87           C  
ATOM    152  CG2 ILE A  55      20.687  65.698  27.338  1.00 29.91           C  
ATOM    153  CD1 ILE A  55      22.827  63.480  28.011  1.00 29.78           C  
ATOM    154  N   VAL A  56      19.117  66.980  30.237  1.00 30.05           N  
ATOM    155  CA  VAL A  56      17.745  67.503  30.215  1.00 30.04           C  
ATOM    156  C   VAL A  56      17.678  68.905  30.826  1.00 29.98           C  
ATOM    157  O   VAL A  56      17.159  69.819  30.185  1.00 30.68           O  
ATOM    158  CB  VAL A  56      16.745  66.553  30.912  1.00 30.51           C  
ATOM    159  CG1 VAL A  56      15.368  67.201  31.045  1.00 30.36           C  
ATOM    160  CG2 VAL A  56      16.629  65.242  30.138  1.00 30.15           C  
ATOM    161  N   ALA A  57      18.206  69.079  32.039  1.00 28.65           N  
ATOM    162  CA  ALA A  57      18.163  70.386  32.711  1.00 28.36           C  
ATOM    163  C   ALA A  57      18.977  71.429  31.959  1.00 27.60           C  
ATOM    164  O   ALA A  57      18.520  72.569  31.785  1.00 28.81           O  
ATOM    165  CB  ALA A  57      18.645  70.290  34.154  1.00 28.39           C  
ATOM    166  N   GLY A  58      20.179  71.043  31.534  1.00 25.68           N  
ATOM    167  CA  GLY A  58      21.040  71.914  30.756  1.00 24.84           C  
ATOM    168  C   GLY A  58      20.331  72.456  29.533  1.00 24.45           C  
ATOM    169  O   GLY A  58      20.298  73.667  29.312  1.00 24.68           O  
ATOM    170  N   ASN A  59      19.728  71.568  28.754  1.00 24.49           N  
ATOM    171  CA  ASN A  59      19.068  71.985  27.507  1.00 25.16           C  
ATOM    172  C   ASN A  59      17.715  72.690  27.669  1.00 26.01           C  
ATOM    173  O   ASN A  59      17.337  73.485  26.798  1.00 26.38           O  
ATOM    174  CB  ASN A  59      19.018  70.833  26.505  1.00 24.90           C  
ATOM    175  CG  ASN A  59      20.373  70.595  25.855  1.00 24.89           C  
ATOM    176  OD1 ASN A  59      20.794  71.370  25.006  1.00 25.42           O  
ATOM    177  ND2 ASN A  59      21.070  69.544  26.267  1.00 24.92           N  
ATOM    178  N   VAL A  60      17.008  72.446  28.776  1.00 26.90           N  
ATOM    179  CA  VAL A  60      15.831  73.265  29.111  1.00 27.39           C  
ATOM    180  C   VAL A  60      16.253  74.711  29.466  1.00 27.52           C  
ATOM    181  O   VAL A  60      15.597  75.676  29.046  1.00 26.46           O  
ATOM    182  CB  VAL A  60      14.988  72.663  30.260  1.00 28.24           C  
ATOM    183  CG1 VAL A  60      13.819  73.575  30.607  1.00 28.37           C  
ATOM    184  CG2 VAL A  60      14.441  71.292  29.885  1.00 28.90           C  
ATOM    185  N   LEU A  61      17.334  74.858  30.232  1.00 27.92           N  
ATOM    186  CA  LEU A  61      17.822  76.189  30.629  1.00 29.17           C  
ATOM    187  C   LEU A  61      18.184  77.040  29.418  1.00 29.23           C  
ATOM    188  O   LEU A  61      17.763  78.200  29.324  1.00 28.45           O  
ATOM    189  CB  LEU A  61      19.030  76.104  31.580  1.00 30.31           C  
ATOM    190  CG  LEU A  61      18.728  75.903  33.068  1.00 32.45           C  
ATOM    191  CD1 LEU A  61      20.021  75.649  33.828  1.00 32.89           C  
ATOM    192  CD2 LEU A  61      17.990  77.106  33.657  1.00 33.02           C  
ATOM    193  N   VAL A  62      18.951  76.449  28.499  1.00 28.28           N  
ATOM    194  CA  VAL A  62      19.322  77.094  27.235  1.00 27.30           C  
ATOM    195  C   VAL A  62      18.080  77.615  26.524  1.00 27.29           C  
ATOM    196  O   VAL A  62      18.020  78.782  26.147  1.00 26.96           O  
ATOM    197  CB  VAL A  62      20.104  76.114  26.324  1.00 26.90           C  
ATOM    198  CG1 VAL A  62      20.189  76.606  24.880  1.00 26.56           C  
ATOM    199  CG2 VAL A  62      21.501  75.898  26.884  1.00 26.93           C  
ATOM    200  N   ILE A  63      17.089  76.742  26.367  1.00 28.01           N  
ATOM    201  CA  ILE A  63      15.825  77.099  25.717  1.00 28.09           C  
ATOM    202  C   ILE A  63      15.050  78.155  26.538  1.00 28.19           C  
ATOM    203  O   ILE A  63      14.457  79.065  25.962  1.00 27.89           O  
ATOM    204  CB  ILE A  63      14.966  75.840  25.444  1.00 28.39           C  
ATOM    205  CG1 ILE A  63      15.688  74.909  24.458  1.00 28.51           C  
ATOM    206  CG2 ILE A  63      13.611  76.220  24.854  1.00 28.78           C  
ATOM    207  CD1 ILE A  63      15.191  73.479  24.466  1.00 28.45           C  
ATOM    208  N   ALA A  64      15.075  78.029  27.868  1.00 28.48           N  
ATOM    209  CA  ALA A  64      14.467  79.012  28.785  1.00 28.30           C  
ATOM    210  C   ALA A  64      15.190  80.364  28.799  1.00 29.02           C  
ATOM    211  O   ALA A  64      14.561  81.400  28.968  1.00 28.62           O  
ATOM    212  CB  ALA A  64      14.412  78.450  30.197  1.00 27.95           C  
ATOM    213  N   ALA A  65      16.513  80.343  28.659  1.00 30.59           N  
ATOM    214  CA  ALA A  65      17.305  81.561  28.528  1.00 31.46           C  
ATOM    215  C   ALA A  65      16.931  82.306  27.259  1.00 33.85           C  
ATOM    216  O   ALA A  65      16.761  83.527  27.283  1.00 36.82           O  
ATOM    217  CB  ALA A  65      18.789  81.236  28.520  1.00 31.29           C  
ATOM    218  N   ILE A  66      16.786  81.567  26.160  1.00 34.74           N  
ATOM    219  CA  ILE A  66      16.485  82.164  24.856  1.00 35.69           C  
ATOM    220  C   ILE A  66      15.063  82.742  24.832  1.00 37.33           C  
ATOM    221  O   ILE A  66      14.857  83.854  24.344  1.00 38.07           O  
ATOM    222  CB  ILE A  66      16.717  81.157  23.697  1.00 34.44           C  
ATOM    223  CG1 ILE A  66      18.205  80.796  23.613  1.00 34.19           C  
ATOM    224  CG2 ILE A  66      16.262  81.743  22.362  1.00 33.98           C  
ATOM    225  CD1 ILE A  66      18.502  79.545  22.818  1.00 34.32           C  
ATOM    226  N   GLY A  67      14.101  81.997  25.373  1.00 38.75           N  
ATOM    227  CA  GLY A  67      12.697  82.418  25.384  1.00 40.23           C  
ATOM    228  C   GLY A  67      12.299  83.480  26.403  1.00 42.37           C  
ATOM    229  O   GLY A  67      11.216  84.060  26.289  1.00 42.56           O  
ATOM    230  N   SER A  68      13.145  83.730  27.406  1.00 44.71           N  
ATOM    231  CA  SER A  68      12.829  84.691  28.473  1.00 46.18           C  
ATOM    232  C   SER A  68      13.681  85.965  28.447  1.00 47.05           C  
ATOM    233  O   SER A  68      13.681  86.718  29.426  1.00 47.81           O  
ATOM    234  CB  SER A  68      12.988  84.013  29.834  1.00 47.05           C  
ATOM    235  OG  SER A  68      14.353  83.930  30.208  1.00 47.75           O  
ATOM    236  N   THR A  69      14.391  86.211  27.344  1.00 47.88           N  
ATOM    237  CA  THR A  69      15.367  87.301  27.270  1.00 48.97           C  
ATOM    238  C   THR A  69      15.342  87.961  25.890  1.00 52.36           C  
ATOM    239  O   THR A  69      15.476  87.278  24.878  1.00 51.21           O  
ATOM    240  CB  THR A  69      16.801  86.789  27.558  1.00 47.82           C  
ATOM    241  OG1 THR A  69      16.782  85.856  28.645  1.00 46.46           O  
ATOM    242  CG2 THR A  69      17.731  87.941  27.912  1.00 47.84           C  
ATOM    243  N   GLN A  70      15.182  89.287  25.874  1.00 56.50           N  
ATOM    244  CA  GLN A  70      15.181  90.101  24.644  1.00 59.91           C  
ATOM    245  C   GLN A  70      16.504  90.014  23.877  1.00 59.86           C  
ATOM    246  O   GLN A  70      16.507  89.831  22.660  1.00 57.80           O  
ATOM    247  CB  GLN A  70      14.881  91.575  24.999  1.00 62.94           C  
ATOM    248  CG  GLN A  70      14.994  92.594  23.864  1.00 64.60           C  
ATOM    249  CD  GLN A  70      14.055  92.312  22.702  1.00 67.08           C  
ATOM    250  OE1 GLN A  70      12.935  91.833  22.896  1.00 67.93           O  
ATOM    251  NE2 GLN A  70      14.499  92.628  21.485  1.00 68.68           N  
ATOM    252  N   ARG A  71      17.611  90.176  24.603  1.00 62.74           N  
ATOM    253  CA  ARG A  71      18.970  90.095  24.037  1.00 64.27           C  
ATOM    254  C   ARG A  71      19.247  88.805  23.252  1.00 61.83           C  
ATOM    255  O   ARG A  71      19.946  88.842  22.235  1.00 59.91           O  
ATOM    256  CB  ARG A  71      20.025  90.228  25.146  1.00 69.17           C  
ATOM    257  CG  ARG A  71      20.352  91.654  25.565  1.00 72.82           C  
ATOM    258  CD  ARG A  71      21.195  91.657  26.838  1.00 76.90           C  
ATOM    259  NE  ARG A  71      22.202  92.722  26.882  1.00 79.59           N  
ATOM    260  CZ  ARG A  71      23.035  92.944  27.904  1.00 81.51           C  
ATOM    261  NH1 ARG A  71      23.000  92.182  29.000  1.00 83.06           N  
ATOM    262  NH2 ARG A  71      23.914  93.941  27.834  1.00 81.30           N  
ATOM    263  N   LEU A  72      18.700  87.680  23.727  1.00 57.77           N  
ATOM    264  CA  LEU A  72      18.912  86.366  23.096  1.00 55.02           C  
ATOM    265  C   LEU A  72      17.879  85.991  22.006  1.00 54.16           C  
ATOM    266  O   LEU A  72      17.874  84.848  21.536  1.00 52.26           O  
ATOM    267  CB  LEU A  72      18.981  85.275  24.180  1.00 53.96           C  
ATOM    268  CG  LEU A  72      20.101  85.408  25.223  1.00 52.91           C  
ATOM    269  CD1 LEU A  72      19.961  84.327  26.282  1.00 52.20           C  
ATOM    270  CD2 LEU A  72      21.482  85.343  24.586  1.00 52.39           C  
ATOM    271  N   GLN A  73      17.049  86.945  21.570  1.00 52.78           N  
ATOM    272  CA  GLN A  73      16.065  86.710  20.503  1.00 53.33           C  
ATOM    273  C   GLN A  73      16.654  86.955  19.107  1.00 51.49           C  
ATOM    274  O   GLN A  73      16.092  87.710  18.310  1.00 52.38           O  
ATOM    275  CB  GLN A  73      14.824  87.596  20.709  1.00 55.81           C  
ATOM    276  CG  GLN A  73      13.974  87.205  21.900  1.00 56.73           C  
ATOM    277  CD  GLN A  73      13.158  85.960  21.629  1.00 58.82           C  
ATOM    278  OE1 GLN A  73      12.078  86.033  21.038  1.00 61.91           O  
ATOM    279  NE2 GLN A  73      13.673  84.806  22.048  1.00 60.09           N  
ATOM    280  N   THR A  74      17.772  86.297  18.808  1.00 48.05           N  
ATOM    281  CA  THR A  74      18.421  86.397  17.504  1.00 45.86           C  
ATOM    282  C   THR A  74      18.027  85.202  16.637  1.00 45.22           C  
ATOM    283  O   THR A  74      17.511  84.200  17.144  1.00 46.13           O  
ATOM    284  CB  THR A  74      19.951  86.467  17.649  1.00 44.48           C  
ATOM    285  OG1 THR A  74      20.416  85.365  18.436  1.00 43.25           O  
ATOM    286  CG2 THR A  74      20.355  87.771  18.320  1.00 43.97           C  
ATOM    287  N   LEU A  75      18.254  85.327  15.330  1.00 43.60           N  
ATOM    288  CA  LEU A  75      17.964  84.247  14.376  1.00 42.99           C  
ATOM    289  C   LEU A  75      18.819  83.012  14.636  1.00 40.77           C  
ATOM    290  O   LEU A  75      18.326  81.884  14.582  1.00 37.83           O  
ATOM    291  CB  LEU A  75      18.182  84.722  12.936  1.00 44.51           C  
ATOM    292  CG  LEU A  75      17.102  85.664  12.403  1.00 45.31           C  
ATOM    293  CD1 LEU A  75      17.615  86.516  11.253  1.00 46.82           C  
ATOM    294  CD2 LEU A  75      15.889  84.870  11.964  1.00 45.81           C  
ATOM    295  N   THR A  76      20.099  83.243  14.912  1.00 39.32           N  
ATOM    296  CA  THR A  76      21.033  82.181  15.262  1.00 39.69           C  
ATOM    297  C   THR A  76      20.554  81.354  16.454  1.00 38.22           C  
ATOM    298  O   THR A  76      20.643  80.127  16.429  1.00 36.92           O  
ATOM    299  CB  THR A  76      22.430  82.760  15.556  1.00 40.76           C  
ATOM    300  OG1 THR A  76      22.886  83.488  14.406  1.00 43.58           O  
ATOM    301  CG2 THR A  76      23.429  81.663  15.866  1.00 41.00           C  
ATOM    302  N   ASN A  77      20.043  82.021  17.486  1.00 37.08           N  
ATOM    303  CA  ASN A  77      19.559  81.322  18.681  1.00 36.28           C  
ATOM    304  C   ASN A  77      18.281  80.501  18.466  1.00 36.49           C  
ATOM    305  O   ASN A  77      18.004  79.580  19.240  1.00 36.02           O  
ATOM    306  CB  ASN A  77      19.410  82.293  19.858  1.00 36.37           C  
ATOM    307  CG  ASN A  77      20.749  82.675  20.475  1.00 35.84           C  
ATOM    308  OD1 ASN A  77      21.791  82.102  20.154  1.00 36.49           O  
ATOM    309  ND2 ASN A  77      20.724  83.639  21.374  1.00 36.16           N  
ATOM    310  N   LEU A  78      17.513  80.827  17.425  1.00 37.18           N  
ATOM    311  CA  LEU A  78      16.460  79.929  16.938  1.00 37.50           C  
ATOM    312  C   LEU A  78      17.052  78.649  16.359  1.00 35.61           C  
ATOM    313  O   LEU A  78      16.492  77.571  16.561  1.00 35.72           O  
ATOM    314  CB  LEU A  78      15.551  80.605  15.900  1.00 40.31           C  
ATOM    315  CG  LEU A  78      14.273  81.230  16.458  1.00 43.15           C  
ATOM    316  CD1 LEU A  78      14.584  82.347  17.443  1.00 44.06           C  
ATOM    317  CD2 LEU A  78      13.420  81.745  15.308  1.00 45.09           C  
ATOM    318  N   PHE A  79      18.165  78.765  15.633  1.00 33.80           N  
ATOM    319  CA  PHE A  79      18.905  77.577  15.189  1.00 33.23           C  
ATOM    320  C   PHE A  79      19.543  76.819  16.364  1.00 31.78           C  
ATOM    321  O   PHE A  79      19.568  75.583  16.352  1.00 31.13           O  
ATOM    322  CB  PHE A  79      19.956  77.912  14.121  1.00 33.37           C  
ATOM    323  CG  PHE A  79      19.379  78.494  12.857  1.00 34.08           C  
ATOM    324  CD1 PHE A  79      18.381  77.825  12.157  1.00 34.96           C  
ATOM    325  CD2 PHE A  79      19.850  79.704  12.349  1.00 34.23           C  
ATOM    326  CE1 PHE A  79      17.847  78.360  10.993  1.00 35.56           C  
ATOM    327  CE2 PHE A  79      19.325  80.242  11.185  1.00 34.68           C  
ATOM    328  CZ  PHE A  79      18.321  79.569  10.505  1.00 35.40           C  
ATOM    329  N   ILE A  80      20.042  77.547  17.368  1.00 29.98           N  
ATOM    330  CA  ILE A  80      20.517  76.932  18.627  1.00 30.20           C  
ATOM    331  C   ILE A  80      19.406  76.117  19.306  1.00 29.24           C  
ATOM    332  O   ILE A  80      19.669  75.037  19.841  1.00 27.80           O  
ATOM    333  CB  ILE A  80      21.079  77.992  19.621  1.00 31.16           C  
ATOM    334  CG1 ILE A  80      22.396  78.598  19.109  1.00 31.73           C  
ATOM    335  CG2 ILE A  80      21.280  77.430  21.029  1.00 31.81           C  
ATOM    336  CD1 ILE A  80      23.555  77.625  19.006  1.00 32.69           C  
ATOM    337  N   THR A  81      18.176  76.639  19.283  1.00 28.76           N  
ATOM    338  CA  THR A  81      17.016  75.944  19.862  1.00 28.15           C  
ATOM    339  C   THR A  81      16.773  74.562  19.232  1.00 27.13           C  
ATOM    340  O   THR A  81      16.378  73.635  19.939  1.00 25.67           O  
ATOM    341  CB  THR A  81      15.749  76.829  19.791  1.00 29.00           C  
ATOM    342  OG1 THR A  81      15.975  78.022  20.555  1.00 29.68           O  
ATOM    343  CG2 THR A  81      14.523  76.117  20.352  1.00 29.78           C  
ATOM    344  N   SER A  82      17.030  74.429  17.925  1.00 26.49           N  
ATOM    345  CA  SER A  82      16.918  73.136  17.222  1.00 26.02           C  
ATOM    346  C   SER A  82      17.929  72.113  17.752  1.00 25.77           C  
ATOM    347  O   SER A  82      17.572  70.954  17.992  1.00 25.24           O  
ATOM    348  CB  SER A  82      17.072  73.320  15.702  1.00 26.71           C  
ATOM    349  OG  SER A  82      17.319  72.093  15.029  1.00 26.81           O  
ATOM    350  N   LEU A  83      19.175  72.546  17.945  1.00 25.64           N  
ATOM    351  CA  LEU A  83      20.209  71.698  18.560  1.00 26.27           C  
ATOM    352  C   LEU A  83      19.802  71.296  19.958  1.00 25.30           C  
ATOM    353  O   LEU A  83      19.874  70.122  20.317  1.00 25.06           O  
ATOM    354  CB  LEU A  83      21.562  72.408  18.636  1.00 27.24           C  
ATOM    355  CG  LEU A  83      22.225  72.773  17.313  1.00 28.37           C  
ATOM    356  CD1 LEU A  83      23.342  73.778  17.543  1.00 29.62           C  
ATOM    357  CD2 LEU A  83      22.756  71.528  16.624  1.00 29.04           C  
ATOM    358  N   ALA A  84      19.366  72.281  20.736  1.00 25.65           N  
ATOM    359  CA  ALA A  84      18.861  72.050  22.094  1.00 25.97           C  
ATOM    360  C   ALA A  84      17.697  71.059  22.130  1.00 26.14           C  
ATOM    361  O   ALA A  84      17.617  70.259  23.049  1.00 26.93           O  
ATOM    362  CB  ALA A  84      18.453  73.368  22.742  1.00 26.10           C  
ATOM    363  N   CYS A  85      16.804  71.116  21.140  1.00 26.93           N  
ATOM    364  CA  CYS A  85      15.706  70.148  21.025  1.00 28.00           C  
ATOM    365  C   CYS A  85      16.220  68.737  20.739  1.00 29.06           C  
ATOM    366  O   CYS A  85      15.727  67.761  21.322  1.00 29.48           O  
ATOM    367  CB  CYS A  85      14.710  70.555  19.930  1.00 28.56           C  
ATOM    368  SG  CYS A  85      13.624  71.927  20.376  1.00 29.79           S  
ATOM    369  N   ALA A  86      17.197  68.631  19.837  1.00 29.28           N  
ATOM    370  CA  ALA A  86      17.827  67.348  19.532  1.00 29.13           C  
ATOM    371  C   ALA A  86      18.555  66.785  20.750  1.00 29.19           C  
ATOM    372  O   ALA A  86      18.464  65.598  21.025  1.00 30.35           O  
ATOM    373  CB  ALA A  86      18.779  67.481  18.353  1.00 29.27           C  
ATOM    374  N   ASP A  87      19.269  67.630  21.482  1.00 29.46           N  
ATOM    375  CA  ASP A  87      19.931  67.188  22.720  1.00 31.19           C  
ATOM    376  C   ASP A  87      18.920  66.764  23.799  1.00 30.98           C  
ATOM    377  O   ASP A  87      19.166  65.829  24.564  1.00 30.25           O  
ATOM    378  CB  ASP A  87      20.863  68.284  23.250  1.00 32.48           C  
ATOM    379  CG  ASP A  87      22.026  68.583  22.300  1.00 34.32           C  
ATOM    380  OD1 ASP A  87      22.409  67.686  21.513  1.00 34.04           O  
ATOM    381  OD2 ASP A  87      22.568  69.713  22.341  1.00 37.33           O  
ATOM    382  N   LEU A  88      17.777  67.442  23.829  1.00 30.90           N  
ATOM    383  CA  LEU A  88      16.690  67.124  24.761  1.00 31.32           C  
ATOM    384  C   LEU A  88      16.042  65.763  24.467  1.00 30.52           C  
ATOM    385  O   LEU A  88      15.765  64.996  25.393  1.00 30.53           O  
ATOM    386  CB  LEU A  88      15.630  68.236  24.723  1.00 31.95           C  
ATOM    387  CG  LEU A  88      14.770  68.528  25.944  1.00 32.05           C  
ATOM    388  CD1 LEU A  88      15.621  68.731  27.187  1.00 32.57           C  
ATOM    389  CD2 LEU A  88      13.944  69.772  25.655  1.00 31.73           C  
ATOM    390  N   VAL A  89      15.812  65.461  23.187  1.00 29.00           N  
ATOM    391  CA  VAL A  89      15.292  64.141  22.788  1.00 28.12           C  
ATOM    392  C   VAL A  89      16.283  63.029  23.159  1.00 27.45           C  
ATOM    393  O   VAL A  89      15.880  61.957  23.606  1.00 28.15           O  
ATOM    394  CB  VAL A  89      14.916  64.102  21.286  1.00 28.48           C  
ATOM    395  CG1 VAL A  89      14.588  62.685  20.815  1.00 28.66           C  
ATOM    396  CG2 VAL A  89      13.715  65.003  21.029  1.00 28.18           C  
ATOM    397  N   VAL A  90      17.575  63.301  22.999  1.00 26.83           N  
ATOM    398  CA  VAL A  90      18.628  62.372  23.421  1.00 26.02           C  
ATOM    399  C   VAL A  90      18.538  62.091  24.927  1.00 25.41           C  
ATOM    400  O   VAL A  90      18.570  60.938  25.346  1.00 25.21           O  
ATOM    401  CB  VAL A  90      20.040  62.889  23.007  1.00 25.34           C  
ATOM    402  CG1 VAL A  90      21.162  62.101  23.665  1.00 24.76           C  
ATOM    403  CG2 VAL A  90      20.194  62.806  21.498  1.00 26.10           C  
ATOM    404  N   GLY A  91      18.420  63.145  25.725  1.00 25.92           N  
ATOM    405  CA  GLY A  91      18.340  63.024  27.182  1.00 26.60           C  
ATOM    406  C   GLY A  91      17.116  62.287  27.708  1.00 27.39           C  
ATOM    407  O   GLY A  91      17.234  61.521  28.661  1.00 27.82           O  
ATOM    408  N   LEU A  92      15.955  62.508  27.082  1.00 28.10           N  
ATOM    409  CA  LEU A  92      14.684  61.924  27.534  1.00 29.18           C  
ATOM    410  C   LEU A  92      14.408  60.531  26.970  1.00 30.68           C  
ATOM    411  O   LEU A  92      13.909  59.666  27.687  1.00 32.24           O  
ATOM    412  CB  LEU A  92      13.502  62.826  27.149  1.00 29.33           C  
ATOM    413  CG  LEU A  92      13.506  64.284  27.634  1.00 29.66           C  
ATOM    414  CD1 LEU A  92      12.482  65.087  26.847  1.00 29.38           C  
ATOM    415  CD2 LEU A  92      13.257  64.404  29.132  1.00 29.56           C  
ATOM    416  N   LEU A  93      14.680  60.328  25.681  1.00 31.33           N  
ATOM    417  CA  LEU A  93      14.290  59.089  24.997  1.00 31.56           C  
ATOM    418  C   LEU A  93      15.476  58.171  24.695  1.00 31.93           C  
ATOM    419  O   LEU A  93      15.428  56.986  25.020  1.00 35.31           O  
ATOM    420  CB  LEU A  93      13.508  59.409  23.726  1.00 31.52           C  
ATOM    421  CG  LEU A  93      12.305  60.352  23.895  1.00 32.26           C  
ATOM    422  CD1 LEU A  93      11.573  60.534  22.576  1.00 32.82           C  
ATOM    423  CD2 LEU A  93      11.328  59.859  24.949  1.00 32.76           C  
ATOM    424  N   VAL A  94      16.551  58.711  24.128  1.00 30.19           N  
ATOM    425  CA  VAL A  94      17.677  57.883  23.697  1.00 28.95           C  
ATOM    426  C   VAL A  94      18.500  57.372  24.881  1.00 28.74           C  
ATOM    427  O   VAL A  94      18.677  56.164  25.018  1.00 29.25           O  
ATOM    428  CB  VAL A  94      18.581  58.606  22.677  1.00 28.54           C  
ATOM    429  CG1 VAL A  94      19.745  57.716  22.253  1.00 28.48           C  
ATOM    430  CG2 VAL A  94      17.769  59.010  21.455  1.00 28.61           C  
ATOM    431  N   VAL A  95      19.000  58.264  25.730  1.00 28.63           N  
ATOM    432  CA  VAL A  95      19.903  57.841  26.815  1.00 29.50           C  
ATOM    433  C   VAL A  95      19.252  56.900  27.853  1.00 30.46           C  
ATOM    434  O   VAL A  95      19.898  55.939  28.273  1.00 31.24           O  
ATOM    435  CB  VAL A  95      20.625  59.049  27.476  1.00 29.28           C  
ATOM    436  CG1 VAL A  95      21.330  58.666  28.777  1.00 29.09           C  
ATOM    437  CG2 VAL A  95      21.641  59.633  26.505  1.00 29.30           C  
ATOM    438  N   PRO A  96      17.989  57.149  28.260  1.00 32.14           N  
ATOM    439  CA  PRO A  96      17.365  56.230  29.231  1.00 33.48           C  
ATOM    440  C   PRO A  96      17.178  54.795  28.734  1.00 35.13           C  
ATOM    441  O   PRO A  96      17.458  53.859  29.479  1.00 36.36           O  
ATOM    442  CB  PRO A  96      16.019  56.905  29.526  1.00 33.09           C  
ATOM    443  CG  PRO A  96      16.326  58.354  29.362  1.00 32.77           C  
ATOM    444  CD  PRO A  96      17.191  58.382  28.125  1.00 32.39           C  
ATOM    445  N   PHE A  97      16.715  54.626  27.496  1.00 36.90           N  
ATOM    446  CA  PHE A  97      16.682  53.300  26.851  1.00 37.35           C  
ATOM    447  C   PHE A  97      18.084  52.688  26.720  1.00 36.71           C  
ATOM    448  O   PHE A  97      18.264  51.482  26.910  1.00 37.94           O  
ATOM    449  CB  PHE A  97      16.061  53.379  25.444  1.00 39.23           C  
ATOM    450  CG  PHE A  97      14.550  53.371  25.411  1.00 40.55           C  
ATOM    451  CD1 PHE A  97      13.817  52.407  26.099  1.00 41.18           C  
ATOM    452  CD2 PHE A  97      13.855  54.296  24.628  1.00 41.44           C  
ATOM    453  CE1 PHE A  97      12.428  52.391  26.042  1.00 41.72           C  
ATOM    454  CE2 PHE A  97      12.467  54.283  24.565  1.00 41.57           C  
ATOM    455  CZ  PHE A  97      11.754  53.324  25.266  1.00 41.79           C  
ATOM    456  N   GLY A  98      19.061  53.515  26.360  1.00 35.58           N  
ATOM    457  CA  GLY A  98      20.446  53.077  26.222  1.00 35.60           C  
ATOM    458  C   GLY A  98      21.078  52.639  27.532  1.00 35.83           C  
ATOM    459  O   GLY A  98      21.778  51.631  27.575  1.00 35.67           O  
ATOM    460  N   ALA A  99      20.833  53.402  28.597  1.00 36.05           N  
ATOM    461  CA  ALA A  99      21.336  53.074  29.942  1.00 35.88           C  
ATOM    462  C   ALA A  99      20.921  51.675  30.387  1.00 35.84           C  
ATOM    463  O   ALA A  99      21.752  50.907  30.869  1.00 36.47           O  
ATOM    464  CB  ALA A  99      20.858  54.102  30.958  1.00 36.05           C  
ATOM    465  N   THR A 100      19.642  51.350  30.199  1.00 35.59           N  
ATOM    466  CA  THR A 100      19.112  50.028  30.540  1.00 35.21           C  
ATOM    467  C   THR A 100      19.763  48.900  29.724  1.00 35.47           C  
ATOM    468  O   THR A 100      19.911  47.796  30.224  1.00 34.74           O  
ATOM    469  CB  THR A 100      17.577  49.948  30.375  1.00 35.14           C  
ATOM    470  OG1 THR A 100      17.208  50.178  29.008  1.00 34.42           O  
ATOM    471  CG2 THR A 100      16.876  50.955  31.292  1.00 34.59           C  
ATOM    472  N   LEU A 101      20.137  49.182  28.477  1.00 37.00           N  
ATOM    473  CA  LEU A 101      20.850  48.215  27.633  1.00 39.65           C  
ATOM    474  C   LEU A 101      22.285  47.980  28.119  1.00 42.06           C  
ATOM    475  O   LEU A 101      22.762  46.840  28.142  1.00 41.58           O  
ATOM    476  CB  LEU A 101      20.857  48.683  26.172  1.00 39.74           C  
ATOM    477  CG  LEU A 101      21.508  47.794  25.110  1.00 39.64           C  
ATOM    478  CD1 LEU A 101      21.063  46.341  25.203  1.00 39.76           C  
ATOM    479  CD2 LEU A 101      21.194  48.346  23.731  1.00 39.97           C  
ATOM    480  N   VAL A 102      22.959  49.059  28.509  1.00 44.99           N  
ATOM    481  CA  VAL A 102      24.314  48.984  29.054  1.00 48.27           C  
ATOM    482  C   VAL A 102      24.326  48.238  30.400  1.00 50.79           C  
ATOM    483  O   VAL A 102      25.115  47.308  30.575  1.00 52.12           O  
ATOM    484  CB  VAL A 102      24.953  50.397  29.186  1.00 49.41           C  
ATOM    485  CG1 VAL A 102      26.260  50.360  29.982  1.00 49.67           C  
ATOM    486  CG2 VAL A 102      25.200  50.996  27.805  1.00 48.17           C  
ATOM    487  N   VAL A 103      23.450  48.625  31.330  1.00 51.94           N  
ATOM    488  CA  VAL A 103      23.478  48.044  32.683  1.00 54.28           C  
ATOM    489  C   VAL A 103      22.987  46.592  32.736  1.00 54.32           C  
ATOM    490  O   VAL A 103      23.614  45.765  33.393  1.00 56.57           O  
ATOM    491  CB  VAL A 103      22.747  48.907  33.752  1.00 55.48           C  
ATOM    492  CG1 VAL A 103      23.320  50.320  33.788  1.00 56.20           C  
ATOM    493  CG2 VAL A 103      21.236  48.926  33.549  1.00 57.06           C  
ATOM    494  N   ARG A 104      21.889  46.272  32.049  1.00 53.94           N  
ATOM    495  CA  ARG A 104      21.365  44.891  32.040  1.00 52.90           C  
ATOM    496  C   ARG A 104      22.065  43.982  31.028  1.00 48.13           C  
ATOM    497  O   ARG A 104      22.068  42.768  31.201  1.00 45.40           O  
ATOM    498  CB  ARG A 104      19.847  44.864  31.808  1.00 55.93           C  
ATOM    499  CG  ARG A 104      19.035  45.435  32.962  1.00 60.42           C  
ATOM    500  CD  ARG A 104      18.926  44.456  34.126  1.00 64.64           C  
ATOM    501  NE  ARG A 104      18.707  45.156  35.400  1.00 70.46           N  
ATOM    502  CZ  ARG A 104      17.638  45.047  36.199  1.00 74.22           C  
ATOM    503  NH1 ARG A 104      16.615  44.240  35.911  1.00 75.05           N  
ATOM    504  NH2 ARG A 104      17.595  45.760  37.326  1.00 75.84           N  
ATOM    505  N   GLY A 105      22.647  44.562  29.978  1.00 45.86           N  
ATOM    506  CA  GLY A 105      23.307  43.786  28.922  1.00 43.24           C  
ATOM    507  C   GLY A 105      22.368  43.126  27.919  1.00 41.26           C  
ATOM    508  O   GLY A 105      22.804  42.293  27.128  1.00 41.40           O  
ATOM    509  N   THR A 106      21.087  43.499  27.943  1.00 39.20           N  
ATOM    510  CA  THR A 106      20.084  43.001  26.991  1.00 36.75           C  
ATOM    511  C   THR A 106      19.006  44.065  26.792  1.00 33.65           C  
ATOM    512  O   THR A 106      18.900  44.997  27.592  1.00 34.55           O  
ATOM    513  CB  THR A 106      19.442  41.670  27.461  1.00 36.98           C  
ATOM    514  OG1 THR A 106      18.375  41.299  26.578  1.00 36.87           O  
ATOM    515  CG2 THR A 106      18.891  41.778  28.882  1.00 37.89           C  
ATOM    516  N   TRP A 107      18.220  43.920  25.729  1.00 30.25           N  
ATOM    517  CA  TRP A 107      17.139  44.854  25.416  1.00 28.39           C  
ATOM    518  C   TRP A 107      15.817  44.358  26.026  1.00 28.22           C  
ATOM    519  O   TRP A 107      15.344  43.273  25.696  1.00 27.40           O  
ATOM    520  CB  TRP A 107      17.016  45.036  23.896  1.00 26.92           C  
ATOM    521  CG  TRP A 107      15.982  46.055  23.480  1.00 24.98           C  
ATOM    522  CD1 TRP A 107      14.759  45.798  22.953  1.00 24.63           C  
ATOM    523  CD2 TRP A 107      16.094  47.479  23.557  1.00 23.90           C  
ATOM    524  NE1 TRP A 107      14.093  46.968  22.700  1.00 24.36           N  
ATOM    525  CE2 TRP A 107      14.891  48.019  23.057  1.00 23.78           C  
ATOM    526  CE3 TRP A 107      17.096  48.355  23.990  1.00 23.78           C  
ATOM    527  CZ2 TRP A 107      14.653  49.397  22.985  1.00 23.62           C  
ATOM    528  CZ3 TRP A 107      16.862  49.738  23.912  1.00 23.37           C  
ATOM    529  CH2 TRP A 107      15.649  50.237  23.413  1.00 23.59           C  
ATOM    530  N   LEU A 108      15.234  45.168  26.907  1.00 28.26           N  
ATOM    531  CA  LEU A 108      14.026  44.804  27.651  1.00 28.71           C  
ATOM    532  C   LEU A 108      12.720  45.239  26.976  1.00 28.43           C  
ATOM    533  O   LEU A 108      11.654  44.730  27.324  1.00 28.94           O  
ATOM    534  CB  LEU A 108      14.066  45.437  29.045  1.00 29.51           C  
ATOM    535  CG  LEU A 108      15.328  45.246  29.890  1.00 30.30           C  
ATOM    536  CD1 LEU A 108      15.261  46.130  31.124  1.00 30.06           C  
ATOM    537  CD2 LEU A 108      15.505  43.785  30.271  1.00 30.88           C  
ATOM    538  N   TRP A 109      12.792  46.155  26.012  1.00 27.35           N  
ATOM    539  CA  TRP A 109      11.607  46.910  25.578  1.00 26.68           C  
ATOM    540  C   TRP A 109      10.922  46.387  24.309  1.00 26.11           C  
ATOM    541  O   TRP A 109      10.027  47.044  23.777  1.00 25.09           O  
ATOM    542  CB  TRP A 109      11.968  48.397  25.469  1.00 26.80           C  
ATOM    543  CG  TRP A 109      12.645  48.846  26.709  1.00 27.28           C  
ATOM    544  CD1 TRP A 109      13.967  49.140  26.863  1.00 27.66           C  
ATOM    545  CD2 TRP A 109      12.055  48.955  28.008  1.00 27.63           C  
ATOM    546  NE1 TRP A 109      14.230  49.472  28.172  1.00 27.40           N  
ATOM    547  CE2 TRP A 109      13.073  49.360  28.897  1.00 28.09           C  
ATOM    548  CE3 TRP A 109      10.758  48.764  28.507  1.00 28.06           C  
ATOM    549  CZ2 TRP A 109      12.831  49.584  30.263  1.00 29.20           C  
ATOM    550  CZ3 TRP A 109      10.518  48.980  29.865  1.00 27.98           C  
ATOM    551  CH2 TRP A 109      11.548  49.387  30.724  1.00 28.53           C  
ATOM    552  N   GLY A 110      11.299  45.193  23.855  1.00 25.54           N  
ATOM    553  CA  GLY A 110      10.662  44.583  22.697  1.00 25.27           C  
ATOM    554  C   GLY A 110      11.153  45.147  21.376  1.00 25.30           C  
ATOM    555  O   GLY A 110      11.878  46.141  21.330  1.00 25.48           O  
ATOM    556  N   SER A 111      10.730  44.504  20.297  1.00 25.22           N  
ATOM    557  CA  SER A 111      11.279  44.757  18.972  1.00 25.76           C  
ATOM    558  C   SER A 111      10.826  46.084  18.371  1.00 26.35           C  
ATOM    559  O   SER A 111      11.601  46.723  17.669  1.00 27.08           O  
ATOM    560  CB  SER A 111      10.946  43.603  18.030  1.00 25.72           C  
ATOM    561  OG  SER A 111       9.548  43.419  17.952  1.00 27.21           O  
ATOM    562  N   PHE A 112       9.592  46.507  18.640  1.00 27.26           N  
ATOM    563  CA  PHE A 112       9.116  47.795  18.118  1.00 28.03           C  
ATOM    564  C   PHE A 112       9.878  48.986  18.703  1.00 27.73           C  
ATOM    565  O   PHE A 112      10.298  49.866  17.966  1.00 28.01           O  
ATOM    566  CB  PHE A 112       7.619  48.010  18.346  1.00 28.45           C  
ATOM    567  CG  PHE A 112       7.170  49.411  18.009  1.00 29.34           C  
ATOM    568  CD1 PHE A 112       7.294  49.894  16.711  1.00 29.66           C  
ATOM    569  CD2 PHE A 112       6.678  50.265  18.989  1.00 29.91           C  
ATOM    570  CE1 PHE A 112       6.911  51.186  16.388  1.00 29.60           C  
ATOM    571  CE2 PHE A 112       6.294  51.561  18.669  1.00 30.28           C  
ATOM    572  CZ  PHE A 112       6.415  52.021  17.369  1.00 29.82           C  
ATOM    573  N   LEU A 113      10.026  49.018  20.022  1.00 27.62           N  
ATOM    574  CA  LEU A 113      10.725  50.114  20.692  1.00 27.58           C  
ATOM    575  C   LEU A 113      12.223  50.121  20.415  1.00 27.05           C  
ATOM    576  O   LEU A 113      12.847  51.169  20.504  1.00 26.00           O  
ATOM    577  CB  LEU A 113      10.481  50.078  22.203  1.00 28.06           C  
ATOM    578  CG  LEU A 113       9.045  50.413  22.607  1.00 29.62           C  
ATOM    579  CD1 LEU A 113       8.812  50.084  24.068  1.00 30.25           C  
ATOM    580  CD2 LEU A 113       8.722  51.884  22.340  1.00 30.12           C  
ATOM    581  N   CYS A 114      12.799  48.957  20.117  1.00 27.47           N  
ATOM    582  CA  CYS A 114      14.167  48.882  19.600  1.00 27.54           C  
ATOM    583  C   CYS A 114      14.280  49.681  18.314  1.00 27.50           C  
ATOM    584  O   CYS A 114      15.212  50.458  18.162  1.00 26.77           O  
ATOM    585  CB  CYS A 114      14.582  47.427  19.337  1.00 27.69           C  
ATOM    586  SG  CYS A 114      16.172  47.224  18.493  1.00 27.85           S  
ATOM    587  N   GLU A 115      13.324  49.480  17.406  1.00 28.72           N  
ATOM    588  CA  GLU A 115      13.307  50.163  16.108  1.00 30.16           C  
ATOM    589  C   GLU A 115      13.025  51.660  16.222  1.00 28.62           C  
ATOM    590  O   GLU A 115      13.642  52.460  15.518  1.00 28.69           O  
ATOM    591  CB  GLU A 115      12.288  49.517  15.165  1.00 33.35           C  
ATOM    592  CG  GLU A 115      12.648  48.099  14.749  1.00 37.55           C  
ATOM    593  CD  GLU A 115      11.684  47.524  13.723  1.00 42.27           C  
ATOM    594  OE1 GLU A 115      10.503  47.269  14.075  1.00 44.88           O  
ATOM    595  OE2 GLU A 115      12.112  47.321  12.561  1.00 45.87           O  
ATOM    596  N   LEU A 116      12.091  52.033  17.093  1.00 26.61           N  
ATOM    597  CA  LEU A 116      11.785  53.435  17.330  1.00 25.94           C  
ATOM    598  C   LEU A 116      12.954  54.147  18.006  1.00 25.22           C  
ATOM    599  O   LEU A 116      13.280  55.278  17.651  1.00 24.21           O  
ATOM    600  CB  LEU A 116      10.528  53.576  18.189  1.00 26.57           C  
ATOM    601  CG  LEU A 116      10.108  55.017  18.519  1.00 27.08           C  
ATOM    602  CD1 LEU A 116       9.698  55.759  17.251  1.00 27.08           C  
ATOM    603  CD2 LEU A 116       8.996  55.042  19.552  1.00 26.65           C  
ATOM    604  N   TRP A 117      13.553  53.484  18.995  1.00 24.88           N  
ATOM    605  CA  TRP A 117      14.726  54.001  19.699  1.00 25.07           C  
ATOM    606  C   TRP A 117      15.854  54.284  18.719  1.00 24.69           C  
ATOM    607  O   TRP A 117      16.423  55.376  18.726  1.00 24.51           O  
ATOM    608  CB  TRP A 117      15.192  53.008  20.771  1.00 25.37           C  
ATOM    609  CG  TRP A 117      16.461  53.378  21.485  1.00 25.89           C  
ATOM    610  CD1 TRP A 117      16.674  54.471  22.287  1.00 26.60           C  
ATOM    611  CD2 TRP A 117      17.688  52.635  21.486  1.00 25.46           C  
ATOM    612  NE1 TRP A 117      17.965  54.455  22.776  1.00 26.65           N  
ATOM    613  CE2 TRP A 117      18.607  53.342  22.298  1.00 25.81           C  
ATOM    614  CE3 TRP A 117      18.100  51.440  20.882  1.00 25.22           C  
ATOM    615  CZ2 TRP A 117      19.914  52.895  22.514  1.00 25.14           C  
ATOM    616  CZ3 TRP A 117      19.399  50.993  21.102  1.00 24.80           C  
ATOM    617  CH2 TRP A 117      20.287  51.718  21.919  1.00 24.96           C  
ATOM    618  N   THR A 118      16.152  53.305  17.871  1.00 24.14           N  
ATOM    619  CA  THR A 118      17.183  53.458  16.850  1.00 24.52           C  
ATOM    620  C   THR A 118      16.878  54.614  15.886  1.00 24.63           C  
ATOM    621  O   THR A 118      17.776  55.389  15.568  1.00 25.42           O  
ATOM    622  CB  THR A 118      17.404  52.154  16.063  1.00 24.55           C  
ATOM    623  OG1 THR A 118      17.582  51.067  16.979  1.00 25.03           O  
ATOM    624  CG2 THR A 118      18.636  52.253  15.199  1.00 24.73           C  
ATOM    625  N   SER A 119      15.625  54.743  15.452  1.00 24.21           N  
ATOM    626  CA  SER A 119      15.221  55.817  14.526  1.00 24.26           C  
ATOM    627  C   SER A 119      15.358  57.224  15.123  1.00 24.22           C  
ATOM    628  O   SER A 119      15.739  58.161  14.425  1.00 24.51           O  
ATOM    629  CB  SER A 119      13.780  55.607  14.044  1.00 24.63           C  
ATOM    630  OG  SER A 119      13.652  54.378  13.339  1.00 25.27           O  
ATOM    631  N   LEU A 120      15.036  57.363  16.406  1.00 24.09           N  
ATOM    632  CA  LEU A 120      15.150  58.645  17.112  1.00 24.29           C  
ATOM    633  C   LEU A 120      16.608  59.023  17.369  1.00 23.62           C  
ATOM    634  O   LEU A 120      16.971  60.204  17.316  1.00 23.04           O  
ATOM    635  CB  LEU A 120      14.411  58.595  18.455  1.00 24.67           C  
ATOM    636  CG  LEU A 120      12.891  58.547  18.406  1.00 25.50           C  
ATOM    637  CD1 LEU A 120      12.352  58.303  19.811  1.00 26.10           C  
ATOM    638  CD2 LEU A 120      12.314  59.828  17.816  1.00 25.53           C  
ATOM    639  N   ASP A 121      17.412  58.012  17.694  1.00 22.53           N  
ATOM    640  CA  ASP A 121      18.854  58.159  17.861  1.00 22.09           C  
ATOM    641  C   ASP A 121      19.473  58.714  16.566  1.00 22.00           C  
ATOM    642  O   ASP A 121      20.158  59.744  16.574  1.00 22.09           O  
ATOM    643  CB  ASP A 121      19.456  56.791  18.227  1.00 21.87           C  
ATOM    644  CG  ASP A 121      20.901  56.873  18.681  1.00 21.62           C  
ATOM    645  OD1 ASP A 121      21.538  57.931  18.497  1.00 21.35           O  
ATOM    646  OD2 ASP A 121      21.406  55.855  19.213  1.00 20.80           O  
ATOM    647  N   VAL A 122      19.184  58.039  15.459  1.00 21.76           N  
ATOM    648  CA  VAL A 122      19.651  58.444  14.122  1.00 21.59           C  
ATOM    649  C   VAL A 122      19.152  59.843  13.716  1.00 21.26           C  
ATOM    650  O   VAL A 122      19.911  60.632  13.140  1.00 20.12           O  
ATOM    651  CB  VAL A 122      19.235  57.398  13.063  1.00 21.22           C  
ATOM    652  CG1 VAL A 122      19.484  57.899  11.647  1.00 21.39           C  
ATOM    653  CG2 VAL A 122      19.992  56.091  13.288  1.00 21.60           C  
ATOM    654  N   LEU A 123      17.881  60.123  14.014  1.00 21.52           N  
ATOM    655  CA  LEU A 123      17.247  61.424  13.737  1.00 21.84           C  
ATOM    656  C   LEU A 123      17.951  62.590  14.418  1.00 21.81           C  
ATOM    657  O   LEU A 123      18.231  63.602  13.774  1.00 21.43           O  
ATOM    658  CB  LEU A 123      15.770  61.407  14.175  1.00 22.34           C  
ATOM    659  CG  LEU A 123      15.001  62.739  14.187  1.00 22.59           C  
ATOM    660  CD1 LEU A 123      14.907  63.314  12.784  1.00 22.79           C  
ATOM    661  CD2 LEU A 123      13.620  62.551  14.792  1.00 22.79           C  
ATOM    662  N   CYS A 124      18.182  62.451  15.725  1.00 22.20           N  
ATOM    663  CA  CYS A 124      18.836  63.487  16.530  1.00 22.90           C  
ATOM    664  C   CYS A 124      20.236  63.832  16.032  1.00 22.29           C  
ATOM    665  O   CYS A 124      20.607  65.007  15.985  1.00 22.78           O  
ATOM    666  CB  CYS A 124      18.910  63.062  17.997  1.00 24.33           C  
ATOM    667  SG  CYS A 124      17.299  63.007  18.810  1.00 27.35           S  
ATOM    668  N   VAL A 125      21.011  62.818  15.656  1.00 21.43           N  
ATOM    669  CA  VAL A 125      22.343  63.065  15.102  1.00 21.25           C  
ATOM    670  C   VAL A 125      22.240  63.801  13.757  1.00 20.82           C  
ATOM    671  O   VAL A 125      23.003  64.738  13.502  1.00 20.31           O  
ATOM    672  CB  VAL A 125      23.157  61.771  14.930  1.00 21.34           C  
ATOM    673  CG1 VAL A 125      24.495  62.069  14.265  1.00 21.53           C  
ATOM    674  CG2 VAL A 125      23.387  61.106  16.284  1.00 21.90           C  
ATOM    675  N   THR A 126      21.290  63.370  12.920  1.00 20.15           N  
ATOM    676  CA  THR A 126      21.108  63.923  11.582  1.00 19.34           C  
ATOM    677  C   THR A 126      20.617  65.362  11.650  1.00 19.67           C  
ATOM    678  O   THR A 126      21.176  66.233  10.991  1.00 20.34           O  
ATOM    679  CB  THR A 126      20.124  63.076  10.757  1.00 18.91           C  
ATOM    680  OG1 THR A 126      20.568  61.712  10.748  1.00 18.57           O  
ATOM    681  CG2 THR A 126      20.029  63.589   9.309  1.00 19.24           C  
ATOM    682  N   ALA A 127      19.583  65.609  12.450  1.00 19.66           N  
ATOM    683  CA  ALA A 127      19.033  66.954  12.601  1.00 19.52           C  
ATOM    684  C   ALA A 127      20.062  67.928  13.188  1.00 19.34           C  
ATOM    685  O   ALA A 127      20.105  69.087  12.800  1.00 19.22           O  
ATOM    686  CB  ALA A 127      17.780  66.915  13.464  1.00 19.63           C  
ATOM    687  N   SER A 128      20.879  67.446  14.126  1.00 19.64           N  
ATOM    688  CA  SER A 128      21.951  68.253  14.740  1.00 19.70           C  
ATOM    689  C   SER A 128      23.000  68.706  13.746  1.00 19.19           C  
ATOM    690  O   SER A 128      23.277  69.894  13.644  1.00 19.06           O  
ATOM    691  CB  SER A 128      22.677  67.469  15.831  1.00 19.69           C  
ATOM    692  OG  SER A 128      21.862  67.290  16.967  1.00 19.88           O  
ATOM    693  N   VAL A 129      23.600  67.752  13.042  1.00 19.20           N  
ATOM    694  CA  VAL A 129      24.685  68.080  12.111  1.00 20.05           C  
ATOM    695  C   VAL A 129      24.212  68.911  10.908  1.00 20.40           C  
ATOM    696  O   VAL A 129      24.952  69.774  10.436  1.00 20.53           O  
ATOM    697  CB  VAL A 129      25.516  66.839  11.684  1.00 20.13           C  
ATOM    698  CG1 VAL A 129      24.715  65.875  10.828  1.00 20.34           C  
ATOM    699  CG2 VAL A 129      26.791  67.271  10.963  1.00 19.94           C  
ATOM    700  N   TRP A 130      22.988  68.672  10.436  1.00 21.11           N  
ATOM    701  CA  TRP A 130      22.406  69.504   9.371  1.00 21.43           C  
ATOM    702  C   TRP A 130      22.067  70.923   9.848  1.00 21.63           C  
ATOM    703  O   TRP A 130      22.195  71.870   9.075  1.00 22.03           O  
ATOM    704  CB  TRP A 130      21.182  68.823   8.724  1.00 21.88           C  
ATOM    705  CG  TRP A 130      21.589  67.878   7.658  1.00 22.14           C  
ATOM    706  CD1 TRP A 130      21.614  66.517   7.727  1.00 22.37           C  
ATOM    707  CD2 TRP A 130      22.094  68.226   6.368  1.00 22.36           C  
ATOM    708  NE1 TRP A 130      22.092  65.994   6.549  1.00 22.49           N  
ATOM    709  CE2 TRP A 130      22.394  67.022   5.698  1.00 22.51           C  
ATOM    710  CE3 TRP A 130      22.325  69.441   5.713  1.00 22.71           C  
ATOM    711  CZ2 TRP A 130      22.903  66.994   4.400  1.00 22.90           C  
ATOM    712  CZ3 TRP A 130      22.839  69.415   4.422  1.00 23.17           C  
ATOM    713  CH2 TRP A 130      23.120  68.199   3.778  1.00 23.11           C  
ATOM    714  N   THR A 131      21.635  71.060  11.103  1.00 21.06           N  
ATOM    715  CA  THR A 131      21.407  72.367  11.720  1.00 20.99           C  
ATOM    716  C   THR A 131      22.714  73.147  11.917  1.00 21.33           C  
ATOM    717  O   THR A 131      22.734  74.369  11.746  1.00 21.73           O  
ATOM    718  CB  THR A 131      20.694  72.233  13.087  1.00 21.14           C  
ATOM    719  OG1 THR A 131      19.410  71.623  12.904  1.00 21.12           O  
ATOM    720  CG2 THR A 131      20.514  73.596  13.765  1.00 20.95           C  
ATOM    721  N   LEU A 132      23.796  72.466  12.296  1.00 21.58           N  
ATOM    722  CA  LEU A 132      25.110  73.128  12.355  1.00 21.99           C  
ATOM    723  C   LEU A 132      25.561  73.574  10.959  1.00 22.95           C  
ATOM    724  O   LEU A 132      26.146  74.657  10.796  1.00 23.53           O  
ATOM    725  CB  LEU A 132      26.171  72.239  12.999  1.00 21.28           C  
ATOM    726  CG  LEU A 132      25.951  71.892  14.473  1.00 21.39           C  
ATOM    727  CD1 LEU A 132      26.881  70.768  14.903  1.00 21.24           C  
ATOM    728  CD2 LEU A 132      26.120  73.103  15.375  1.00 21.49           C  
ATOM    729  N   CYS A 133      25.271  72.751   9.959  1.00 23.23           N  
ATOM    730  CA  CYS A 133      25.523  73.124   8.575  1.00 25.08           C  
ATOM    731  C   CYS A 133      24.700  74.349   8.108  1.00 24.58           C  
ATOM    732  O   CYS A 133      25.230  75.209   7.401  1.00 24.68           O  
ATOM    733  CB  CYS A 133      25.279  71.933   7.666  1.00 26.56           C  
ATOM    734  SG  CYS A 133      25.700  72.309   5.972  1.00 31.92           S  
ATOM    735  N   VAL A 134      23.429  74.430   8.511  1.00 23.77           N  
ATOM    736  CA  VAL A 134      22.594  75.614   8.256  1.00 24.11           C  
ATOM    737  C   VAL A 134      23.143  76.867   8.959  1.00 24.22           C  
ATOM    738  O   VAL A 134      23.193  77.933   8.355  1.00 24.13           O  
ATOM    739  CB  VAL A 134      21.113  75.387   8.677  1.00 24.51           C  
ATOM    740  CG1 VAL A 134      20.302  76.683   8.628  1.00 24.38           C  
ATOM    741  CG2 VAL A 134      20.452  74.347   7.782  1.00 24.48           C  
ATOM    742  N   ILE A 135      23.536  76.730  10.227  1.00 24.88           N  
ATOM    743  CA  ILE A 135      24.138  77.832  11.002  1.00 24.38           C  
ATOM    744  C   ILE A 135      25.397  78.392  10.333  1.00 23.87           C  
ATOM    745  O   ILE A 135      25.568  79.607  10.267  1.00 22.72           O  
ATOM    746  CB  ILE A 135      24.448  77.405  12.463  1.00 24.82           C  
ATOM    747  CG1 ILE A 135      23.141  77.276  13.251  1.00 24.80           C  
ATOM    748  CG2 ILE A 135      25.374  78.409  13.166  1.00 25.05           C  
ATOM    749  CD1 ILE A 135      23.275  76.546  14.572  1.00 24.82           C  
ATOM    750  N   ALA A 136      26.270  77.514   9.846  1.00 24.29           N  
ATOM    751  CA  ALA A 136      27.498  77.950   9.163  1.00 24.73           C  
ATOM    752  C   ALA A 136      27.168  78.763   7.922  1.00 25.75           C  
ATOM    753  O   ALA A 136      27.727  79.842   7.718  1.00 25.76           O  
ATOM    754  CB  ALA A 136      28.370  76.761   8.792  1.00 24.45           C  
ATOM    755  N   ILE A 137      26.242  78.243   7.113  1.00 26.74           N  
ATOM    756  CA  ILE A 137      25.824  78.892   5.861  1.00 27.22           C  
ATOM    757  C   ILE A 137      25.119  80.228   6.120  1.00 26.91           C  
ATOM    758  O   ILE A 137      25.400  81.216   5.449  1.00 26.88           O  
ATOM    759  CB  ILE A 137      24.929  77.945   5.017  1.00 27.89           C  
ATOM    760  CG1 ILE A 137      25.765  76.770   4.490  1.00 28.20           C  
ATOM    761  CG2 ILE A 137      24.274  78.677   3.845  1.00 27.90           C  
ATOM    762  CD1 ILE A 137      24.945  75.588   4.006  1.00 28.36           C  
ATOM    763  N   ASP A 138      24.198  80.223   7.080  1.00 27.83           N  
ATOM    764  CA  ASP A 138      23.461  81.406   7.521  1.00 28.60           C  
ATOM    765  C   ASP A 138      24.420  82.545   7.876  1.00 30.32           C  
ATOM    766  O   ASP A 138      24.313  83.653   7.341  1.00 31.25           O  
ATOM    767  CB  ASP A 138      22.611  81.023   8.738  1.00 28.85           C  
ATOM    768  CG  ASP A 138      21.838  82.195   9.324  1.00 29.69           C  
ATOM    769  OD1 ASP A 138      20.830  82.613   8.724  1.00 31.50           O  
ATOM    770  OD2 ASP A 138      22.204  82.671  10.415  1.00 29.12           O  
ATOM    771  N   ARG A 139      25.375  82.239   8.757  1.00 31.13           N  
ATOM    772  CA  ARG A 139      26.342  83.218   9.250  1.00 30.30           C  
ATOM    773  C   ARG A 139      27.276  83.722   8.163  1.00 30.52           C  
ATOM    774  O   ARG A 139      27.604  84.902   8.155  1.00 30.58           O  
ATOM    775  CB  ARG A 139      27.159  82.650  10.421  1.00 30.03           C  
ATOM    776  CG  ARG A 139      26.383  82.449  11.718  1.00 30.34           C  
ATOM    777  CD  ARG A 139      25.737  83.734  12.209  1.00 30.95           C  
ATOM    778  NE  ARG A 139      24.371  83.924  11.700  1.00 31.84           N  
ATOM    779  CZ  ARG A 139      23.695  85.078  11.706  1.00 33.09           C  
ATOM    780  NH1 ARG A 139      24.231  86.183  12.177  1.00 33.38           N  
ATOM    781  NH2 ARG A 139      22.457  85.137  11.227  1.00 34.27           N  
ATOM    782  N   TYR A 140      27.705  82.841   7.261  1.00 31.83           N  
ATOM    783  CA  TYR A 140      28.477  83.262   6.080  1.00 33.56           C  
ATOM    784  C   TYR A 140      27.735  84.321   5.264  1.00 34.02           C  
ATOM    785  O   TYR A 140      28.310  85.352   4.925  1.00 32.59           O  
ATOM    786  CB  TYR A 140      28.820  82.081   5.171  1.00 34.17           C  
ATOM    787  CG  TYR A 140      29.707  82.497   4.021  1.00 37.34           C  
ATOM    788  CD1 TYR A 140      31.073  82.724   4.216  1.00 39.14           C  
ATOM    789  CD2 TYR A 140      29.179  82.705   2.741  1.00 38.97           C  
ATOM    790  CE1 TYR A 140      31.891  83.124   3.164  1.00 40.84           C  
ATOM    791  CE2 TYR A 140      29.986  83.107   1.686  1.00 39.67           C  
ATOM    792  CZ  TYR A 140      31.338  83.315   1.897  1.00 41.24           C  
ATOM    793  OH  TYR A 140      32.139  83.712   0.848  1.00 43.50           O  
ATOM    794  N   LEU A 141      26.461  84.063   4.972  1.00 34.93           N  
ATOM    795  CA  LEU A 141      25.639  85.016   4.229  1.00 37.13           C  
ATOM    796  C   LEU A 141      25.381  86.287   5.035  1.00 37.56           C  
ATOM    797  O   LEU A 141      25.342  87.383   4.469  1.00 38.81           O  
ATOM    798  CB  LEU A 141      24.316  84.375   3.786  1.00 37.06           C  
ATOM    799  CG  LEU A 141      24.466  83.210   2.803  1.00 38.03           C  
ATOM    800  CD1 LEU A 141      23.132  82.512   2.586  1.00 39.08           C  
ATOM    801  CD2 LEU A 141      25.056  83.669   1.476  1.00 38.29           C  
ATOM    802  N   ALA A 142      25.222  86.132   6.348  1.00 37.50           N  
ATOM    803  CA  ALA A 142      25.028  87.266   7.244  1.00 38.34           C  
ATOM    804  C   ALA A 142      26.224  88.240   7.270  1.00 39.99           C  
ATOM    805  O   ALA A 142      26.022  89.451   7.190  1.00 39.76           O  
ATOM    806  CB  ALA A 142      24.699  86.776   8.644  1.00 38.01           C  
ATOM    807  N   ILE A 143      27.453  87.727   7.378  1.00 41.31           N  
ATOM    808  CA  ILE A 143      28.651  88.606   7.355  1.00 43.07           C  
ATOM    809  C   ILE A 143      28.998  89.171   5.974  1.00 42.81           C  
ATOM    810  O   ILE A 143      29.435  90.317   5.884  1.00 42.85           O  
ATOM    811  CB  ILE A 143      29.936  87.966   7.965  1.00 45.19           C  
ATOM    812  CG1 ILE A 143      30.357  86.681   7.236  1.00 46.04           C  
ATOM    813  CG2 ILE A 143      29.765  87.760   9.464  1.00 46.29           C  
ATOM    814  CD1 ILE A 143      31.603  86.051   7.815  1.00 48.20           C  
ATOM    815  N   THR A 144      28.817  88.373   4.918  1.00 42.50           N  
ATOM    816  CA  THR A 144      29.173  88.785   3.550  1.00 42.09           C  
ATOM    817  C   THR A 144      28.122  89.678   2.882  1.00 43.41           C  
ATOM    818  O   THR A 144      28.466  90.472   2.007  1.00 44.44           O  
ATOM    819  CB  THR A 144      29.445  87.577   2.628  1.00 40.52           C  
ATOM    820  OG1 THR A 144      28.320  86.692   2.637  1.00 38.74           O  
ATOM    821  CG2 THR A 144      30.688  86.828   3.077  1.00 40.49           C  
ATOM    822  N   SER A 145      26.856  89.527   3.271  1.00 43.41           N  
ATOM    823  CA  SER A 145      25.780  90.402   2.804  1.00 45.06           C  
ATOM    824  C   SER A 145      24.860  90.778   3.968  1.00 44.98           C  
ATOM    825  O   SER A 145      23.700  90.364   4.001  1.00 43.96           O  
ATOM    826  CB  SER A 145      24.979  89.721   1.689  1.00 46.33           C  
ATOM    827  OG  SER A 145      25.795  89.461   0.562  1.00 50.75           O  
ATOM    828  N   PRO A 146      25.367  91.582   4.926  1.00 45.89           N  
ATOM    829  CA  PRO A 146      24.532  91.972   6.077  1.00 47.01           C  
ATOM    830  C   PRO A 146      23.301  92.790   5.692  1.00 48.55           C  
ATOM    831  O   PRO A 146      22.279  92.734   6.373  1.00 46.82           O  
ATOM    832  CB  PRO A 146      25.479  92.818   6.948  1.00 46.44           C  
ATOM    833  CG  PRO A 146      26.830  92.737   6.326  1.00 46.63           C  
ATOM    834  CD  PRO A 146      26.646  92.315   4.902  1.00 46.48           C  
ATOM    835  N   PHE A 147      23.412  93.516   4.585  1.00 52.79           N  
ATOM    836  CA  PHE A 147      22.378  94.427   4.115  1.00 55.70           C  
ATOM    837  C   PHE A 147      21.197  93.613   3.581  1.00 53.84           C  
ATOM    838  O   PHE A 147      20.062  93.769   4.044  1.00 50.74           O  
ATOM    839  CB  PHE A 147      22.964  95.361   3.040  1.00 59.04           C  
ATOM    840  CG  PHE A 147      24.232  96.071   3.475  1.00 62.41           C  
ATOM    841  CD1 PHE A 147      24.166  97.200   4.280  1.00 64.21           C  
ATOM    842  CD2 PHE A 147      25.492  95.596   3.100  1.00 63.23           C  
ATOM    843  CE1 PHE A 147      25.320  97.856   4.696  1.00 65.00           C  
ATOM    844  CE2 PHE A 147      26.652  96.244   3.515  1.00 64.47           C  
ATOM    845  CZ  PHE A 147      26.566  97.379   4.313  1.00 65.27           C  
ATOM    846  N   ARG A 148      21.487  92.721   2.636  1.00 53.71           N  
ATOM    847  CA  ARG A 148      20.487  91.803   2.092  1.00 54.54           C  
ATOM    848  C   ARG A 148      19.925  90.883   3.167  1.00 54.94           C  
ATOM    849  O   ARG A 148      18.701  90.764   3.310  1.00 54.60           O  
ATOM    850  CB  ARG A 148      21.094  90.954   0.979  1.00 56.63           C  
ATOM    851  CG  ARG A 148      20.153  89.902   0.399  1.00 59.88           C  
ATOM    852  CD  ARG A 148      20.754  89.199  -0.807  1.00 62.80           C  
ATOM    853  NE  ARG A 148      21.257  90.154  -1.793  1.00 65.39           N  
ATOM    854  CZ  ARG A 148      20.499  90.894  -2.605  1.00 69.08           C  
ATOM    855  NH1 ARG A 148      19.165  90.817  -2.580  1.00 70.01           N  
ATOM    856  NH2 ARG A 148      21.085  91.734  -3.458  1.00 70.29           N  
ATOM    857  N   TYR A 149      20.825  90.231   3.907  1.00 53.28           N  
ATOM    858  CA  TYR A 149      20.443  89.254   4.929  1.00 50.47           C  
ATOM    859  C   TYR A 149      19.369  89.794   5.864  1.00 54.57           C  
ATOM    860  O   TYR A 149      18.380  89.117   6.135  1.00 55.08           O  
ATOM    861  CB  TYR A 149      21.656  88.802   5.761  1.00 46.98           C  
ATOM    862  CG  TYR A 149      21.288  87.767   6.803  1.00 43.48           C  
ATOM    863  CD1 TYR A 149      20.836  88.149   8.069  1.00 41.59           C  
ATOM    864  CD2 TYR A 149      21.347  86.408   6.512  1.00 41.38           C  
ATOM    865  CE1 TYR A 149      20.465  87.211   9.016  1.00 39.76           C  
ATOM    866  CE2 TYR A 149      20.987  85.462   7.457  1.00 40.41           C  
ATOM    867  CZ  TYR A 149      20.542  85.869   8.711  1.00 39.93           C  
ATOM    868  OH  TYR A 149      20.173  84.953   9.676  1.00 38.43           O  
ATOM    869  N   GLN A 150      19.575  91.014   6.349  1.00 60.40           N  
ATOM    870  CA  GLN A 150      18.716  91.591   7.384  1.00 65.23           C  
ATOM    871  C   GLN A 150      17.356  92.042   6.833  1.00 64.12           C  
ATOM    872  O   GLN A 150      16.358  91.996   7.555  1.00 62.77           O  
ATOM    873  CB  GLN A 150      19.445  92.741   8.093  1.00 69.37           C  
ATOM    874  CG  GLN A 150      19.041  92.950   9.547  1.00 75.15           C  
ATOM    875  CD  GLN A 150      20.095  93.697  10.351  1.00 80.33           C  
ATOM    876  OE1 GLN A 150      21.007  94.308   9.789  1.00 84.60           O  
ATOM    877  NE2 GLN A 150      19.976  93.651  11.677  1.00 83.43           N  
ATOM    878  N   SER A 151      17.314  92.459   5.566  1.00 64.27           N  
ATOM    879  CA  SER A 151      16.041  92.796   4.910  1.00 65.70           C  
ATOM    880  C   SER A 151      15.235  91.545   4.522  1.00 64.33           C  
ATOM    881  O   SER A 151      14.006  91.593   4.494  1.00 63.98           O  
ATOM    882  CB  SER A 151      16.263  93.697   3.683  1.00 65.74           C  
ATOM    883  OG  SER A 151      16.603  92.951   2.526  1.00 67.63           O  
ATOM    884  N   LEU A 152      15.926  90.435   4.243  1.00 64.80           N  
ATOM    885  CA  LEU A 152      15.296  89.222   3.702  1.00 65.82           C  
ATOM    886  C   LEU A 152      14.974  88.130   4.742  1.00 65.25           C  
ATOM    887  O   LEU A 152      13.914  87.511   4.659  1.00 68.63           O  
ATOM    888  CB  LEU A 152      16.176  88.650   2.584  1.00 66.68           C  
ATOM    889  CG  LEU A 152      15.592  87.592   1.638  1.00 68.28           C  
ATOM    890  CD1 LEU A 152      14.218  87.973   1.097  1.00 68.10           C  
ATOM    891  CD2 LEU A 152      16.562  87.339   0.489  1.00 68.10           C  
ATOM    892  N   MET A 153      15.869  87.888   5.704  1.00 63.09           N  
ATOM    893  CA  MET A 153      15.635  86.851   6.727  1.00 60.72           C  
ATOM    894  C   MET A 153      14.754  87.370   7.855  1.00 60.65           C  
ATOM    895  O   MET A 153      14.941  88.489   8.327  1.00 59.18           O  
ATOM    896  CB  MET A 153      16.950  86.303   7.309  1.00 60.32           C  
ATOM    897  CG  MET A 153      17.566  85.160   6.511  1.00 59.52           C  
ATOM    898  SD  MET A 153      16.607  83.627   6.547  1.00 60.92           S  
ATOM    899  CE  MET A 153      16.755  83.139   8.263  1.00 60.30           C  
ATOM    900  N   THR A 154      13.799  86.539   8.272  1.00 62.20           N  
ATOM    901  CA  THR A 154      12.898  86.835   9.388  1.00 63.05           C  
ATOM    902  C   THR A 154      12.815  85.645  10.342  1.00 63.35           C  
ATOM    903  O   THR A 154      13.221  84.529  10.004  1.00 60.95           O  
ATOM    904  CB  THR A 154      11.470  87.160   8.898  1.00 62.56           C  
ATOM    905  OG1 THR A 154      10.952  86.055   8.147  1.00 62.24           O  
ATOM    906  CG2 THR A 154      11.464  88.414   8.034  1.00 61.47           C  
ATOM    907  N   ARG A 155      12.276  85.911  11.530  1.00 65.08           N  
ATOM    908  CA  ARG A 155      12.089  84.906  12.583  1.00 66.12           C  
ATOM    909  C   ARG A 155      11.243  83.717  12.109  1.00 65.91           C  
ATOM    910  O   ARG A 155      11.516  82.572  12.474  1.00 66.35           O  
ATOM    911  CB  ARG A 155      11.439  85.557  13.810  1.00 69.13           C  
ATOM    912  CG  ARG A 155      11.579  84.762  15.099  1.00 72.93           C  
ATOM    913  CD  ARG A 155      11.239  85.596  16.333  1.00 74.44           C  
ATOM    914  NE  ARG A 155      12.046  86.815  16.428  1.00 75.06           N  
ATOM    915  CZ  ARG A 155      13.338  86.868  16.762  1.00 76.62           C  
ATOM    916  NH1 ARG A 155      14.029  85.767  17.057  1.00 77.09           N  
ATOM    917  NH2 ARG A 155      13.951  88.047  16.804  1.00 78.48           N  
ATOM    918  N   ALA A 156      10.227  84.002  11.295  1.00 65.16           N  
ATOM    919  CA  ALA A 156       9.365  82.970  10.712  1.00 63.61           C  
ATOM    920  C   ALA A 156      10.083  82.124   9.656  1.00 62.51           C  
ATOM    921  O   ALA A 156       9.882  80.908   9.598  1.00 66.60           O  
ATOM    922  CB  ALA A 156       8.113  83.602  10.115  1.00 63.55           C  
ATOM    923  N   ARG A 157      10.907  82.760   8.823  1.00 57.73           N  
ATOM    924  CA  ARG A 157      11.668  82.039   7.796  1.00 56.16           C  
ATOM    925  C   ARG A 157      12.728  81.093   8.389  1.00 54.18           C  
ATOM    926  O   ARG A 157      13.037  80.054   7.795  1.00 52.39           O  
ATOM    927  CB  ARG A 157      12.318  83.022   6.821  1.00 58.16           C  
ATOM    928  CG  ARG A 157      13.031  82.358   5.652  1.00 60.38           C  
ATOM    929  CD  ARG A 157      13.252  83.317   4.496  1.00 62.76           C  
ATOM    930  NE  ARG A 157      14.330  82.871   3.610  1.00 65.45           N  
ATOM    931  CZ  ARG A 157      14.678  83.465   2.467  1.00 68.03           C  
ATOM    932  NH1 ARG A 157      14.034  84.547   2.026  1.00 69.91           N  
ATOM    933  NH2 ARG A 157      15.678  82.966   1.748  1.00 68.99           N  
ATOM    934  N   ALA A 158      13.282  81.458   9.547  1.00 51.91           N  
ATOM    935  CA  ALA A 158      14.175  80.574  10.303  1.00 49.23           C  
ATOM    936  C   ALA A 158      13.453  79.300  10.748  1.00 47.28           C  
ATOM    937  O   ALA A 158      13.969  78.200  10.545  1.00 46.63           O  
ATOM    938  CB  ALA A 158      14.760  81.300  11.507  1.00 49.21           C  
ATOM    939  N   LYS A 159      12.264  79.456  11.337  1.00 46.11           N  
ATOM    940  CA  LYS A 159      11.430  78.313  11.766  1.00 46.17           C  
ATOM    941  C   LYS A 159      11.111  77.344  10.621  1.00 43.38           C  
ATOM    942  O   LYS A 159      11.124  76.124  10.807  1.00 43.12           O  
ATOM    943  CB  LYS A 159      10.111  78.790  12.389  1.00 48.53           C  
ATOM    944  CG  LYS A 159      10.227  79.401  13.780  1.00 50.56           C  
ATOM    945  CD  LYS A 159       8.855  79.839  14.288  1.00 52.67           C  
ATOM    946  CE  LYS A 159       8.775  79.886  15.806  1.00 54.64           C  
ATOM    947  NZ  LYS A 159       9.450  81.089  16.362  1.00 57.12           N  
ATOM    948  N   VAL A 160      10.828  77.900   9.446  1.00 41.05           N  
ATOM    949  CA  VAL A 160      10.552  77.110   8.241  1.00 38.99           C  
ATOM    950  C   VAL A 160      11.763  76.264   7.837  1.00 37.41           C  
ATOM    951  O   VAL A 160      11.617  75.082   7.497  1.00 37.67           O  
ATOM    952  CB  VAL A 160      10.097  78.024   7.067  1.00 39.28           C  
ATOM    953  CG1 VAL A 160      10.106  77.292   5.721  1.00 38.10           C  
ATOM    954  CG2 VAL A 160       8.710  78.585   7.351  1.00 38.97           C  
ATOM    955  N   ILE A 161      12.949  76.871   7.868  1.00 35.59           N  
ATOM    956  CA  ILE A 161      14.194  76.147   7.573  1.00 34.55           C  
ATOM    957  C   ILE A 161      14.417  75.015   8.585  1.00 33.27           C  
ATOM    958  O   ILE A 161      14.765  73.901   8.200  1.00 31.30           O  
ATOM    959  CB  ILE A 161      15.423  77.087   7.538  1.00 34.42           C  
ATOM    960  CG1 ILE A 161      15.328  78.042   6.339  1.00 34.54           C  
ATOM    961  CG2 ILE A 161      16.722  76.282   7.451  1.00 34.44           C  
ATOM    962  CD1 ILE A 161      16.189  79.283   6.461  1.00 34.53           C  
ATOM    963  N   ILE A 162      14.194  75.313   9.864  1.00 32.35           N  
ATOM    964  CA  ILE A 162      14.319  74.324  10.938  1.00 32.38           C  
ATOM    965  C   ILE A 162      13.363  73.147  10.708  1.00 33.02           C  
ATOM    966  O   ILE A 162      13.760  71.987  10.858  1.00 32.14           O  
ATOM    967  CB  ILE A 162      14.083  74.963  12.334  1.00 32.12           C  
ATOM    968  CG1 ILE A 162      15.211  75.950  12.660  1.00 32.11           C  
ATOM    969  CG2 ILE A 162      14.015  73.895  13.423  1.00 32.22           C  
ATOM    970  CD1 ILE A 162      14.932  76.853  13.840  1.00 32.16           C  
ATOM    971  N   CYS A 163      12.116  73.457  10.340  1.00 33.73           N  
ATOM    972  CA ACYS A 163      11.103  72.440  10.031  0.50 33.30           C  
ATOM    973  CA BCYS A 163      11.124  72.420  10.055  0.50 33.55           C  
ATOM    974  C   CYS A 163      11.529  71.559   8.859  1.00 32.73           C  
ATOM    975  O   CYS A 163      11.373  70.343   8.901  1.00 33.89           O  
ATOM    976  CB ACYS A 163       9.753  73.103   9.717  0.50 33.87           C  
ATOM    977  CB BCYS A 163       9.730  73.024   9.847  0.50 34.41           C  
ATOM    978  SG ACYS A 163       8.421  71.960   9.269  0.50 33.57           S  
ATOM    979  SG BCYS A 163       8.925  73.498  11.395  0.50 34.82           S  
ATOM    980  N   THR A 164      12.056  72.181   7.808  1.00 31.59           N  
ATOM    981  CA  THR A 164      12.540  71.438   6.635  1.00 31.46           C  
ATOM    982  C   THR A 164      13.700  70.491   7.004  1.00 31.34           C  
ATOM    983  O   THR A 164      13.704  69.329   6.589  1.00 33.01           O  
ATOM    984  CB  THR A 164      12.964  72.397   5.506  1.00 32.17           C  
ATOM    985  OG1 THR A 164      11.891  73.304   5.232  1.00 32.89           O  
ATOM    986  CG2 THR A 164      13.312  71.646   4.226  1.00 32.42           C  
ATOM    987  N   VAL A 165      14.650  70.980   7.805  1.00 29.67           N  
ATOM    988  CA  VAL A 165      15.721  70.143   8.353  1.00 29.20           C  
ATOM    989  C   VAL A 165      15.150  68.909   9.086  1.00 29.43           C  
ATOM    990  O   VAL A 165      15.477  67.775   8.727  1.00 28.49           O  
ATOM    991  CB  VAL A 165      16.676  70.946   9.281  1.00 29.05           C  
ATOM    992  CG1 VAL A 165      17.617  70.025  10.059  1.00 28.67           C  
ATOM    993  CG2 VAL A 165      17.493  71.947   8.471  1.00 29.04           C  
ATOM    994  N   TRP A 166      14.298  69.128  10.088  1.00 29.16           N  
ATOM    995  CA  TRP A 166      13.706  68.009  10.847  1.00 29.86           C  
ATOM    996  C   TRP A 166      12.789  67.096  10.008  1.00 31.32           C  
ATOM    997  O   TRP A 166      12.729  65.890  10.250  1.00 30.97           O  
ATOM    998  CB  TRP A 166      12.950  68.513  12.082  1.00 29.46           C  
ATOM    999  CG  TRP A 166      13.841  68.912  13.239  1.00 29.24           C  
ATOM   1000  CD1 TRP A 166      14.437  70.123  13.440  1.00 28.98           C  
ATOM   1001  CD2 TRP A 166      14.211  68.098  14.362  1.00 29.04           C  
ATOM   1002  NE1 TRP A 166      15.156  70.116  14.611  1.00 28.14           N  
ATOM   1003  CE2 TRP A 166      15.035  68.886  15.197  1.00 28.71           C  
ATOM   1004  CE3 TRP A 166      13.928  66.780  14.742  1.00 29.11           C  
ATOM   1005  CZ2 TRP A 166      15.582  68.396  16.390  1.00 29.53           C  
ATOM   1006  CZ3 TRP A 166      14.473  66.292  15.932  1.00 29.30           C  
ATOM   1007  CH2 TRP A 166      15.291  67.098  16.738  1.00 29.23           C  
ATOM   1008  N   ALA A 167      12.085  67.670   9.031  1.00 33.09           N  
ATOM   1009  CA  ALA A 167      11.240  66.895   8.117  1.00 33.21           C  
ATOM   1010  C   ALA A 167      12.072  66.006   7.192  1.00 33.86           C  
ATOM   1011  O   ALA A 167      11.782  64.815   7.075  1.00 35.24           O  
ATOM   1012  CB  ALA A 167      10.336  67.811   7.308  1.00 33.32           C  
ATOM   1013  N   ILE A 168      13.113  66.560   6.561  1.00 34.40           N  
ATOM   1014  CA  ILE A 168      14.015  65.741   5.723  1.00 34.68           C  
ATOM   1015  C   ILE A 168      14.778  64.735   6.594  1.00 33.57           C  
ATOM   1016  O   ILE A 168      14.857  63.558   6.244  1.00 33.99           O  
ATOM   1017  CB  ILE A 168      15.031  66.559   4.888  1.00 35.92           C  
ATOM   1018  CG1 ILE A 168      14.333  67.559   3.956  1.00 37.08           C  
ATOM   1019  CG2 ILE A 168      15.877  65.624   4.019  1.00 35.97           C  
ATOM   1020  CD1 ILE A 168      15.225  68.714   3.546  1.00 37.87           C  
ATOM   1021  N   SER A 169      15.327  65.194   7.721  1.00 32.53           N  
ATOM   1022  CA  SER A 169      16.029  64.306   8.663  1.00 31.36           C  
ATOM   1023  C   SER A 169      15.169  63.106   9.035  1.00 30.90           C  
ATOM   1024  O   SER A 169      15.643  61.982   9.004  1.00 29.74           O  
ATOM   1025  CB  SER A 169      16.455  65.051   9.931  1.00 30.70           C  
ATOM   1026  OG  SER A 169      17.465  65.995   9.639  1.00 30.44           O  
ATOM   1027  N   ALA A 170      13.904  63.355   9.360  1.00 32.26           N  
ATOM   1028  CA  ALA A 170      12.947  62.284   9.675  1.00 34.10           C  
ATOM   1029  C   ALA A 170      12.703  61.335   8.496  1.00 36.17           C  
ATOM   1030  O   ALA A 170      12.653  60.119   8.693  1.00 35.02           O  
ATOM   1031  CB  ALA A 170      11.633  62.871  10.157  1.00 34.39           C  
ATOM   1032  N   LEU A 171      12.568  61.888   7.284  1.00 38.95           N  
ATOM   1033  CA  LEU A 171      12.476  61.077   6.051  1.00 41.26           C  
ATOM   1034  C   LEU A 171      13.658  60.115   5.945  1.00 41.48           C  
ATOM   1035  O   LEU A 171      13.466  58.893   5.980  1.00 41.12           O  
ATOM   1036  CB  LEU A 171      12.395  61.965   4.787  1.00 43.85           C  
ATOM   1037  CG  LEU A 171      12.693  61.344   3.405  1.00 46.14           C  
ATOM   1038  CD1 LEU A 171      11.556  60.430   2.978  1.00 46.95           C  
ATOM   1039  CD2 LEU A 171      12.953  62.410   2.345  1.00 47.05           C  
ATOM   1040  N   VAL A 172      14.869  60.674   5.842  1.00 40.87           N  
ATOM   1041  CA  VAL A 172      16.088  59.864   5.676  1.00 40.65           C  
ATOM   1042  C   VAL A 172      16.392  58.946   6.871  1.00 39.47           C  
ATOM   1043  O   VAL A 172      17.066  57.933   6.697  1.00 41.55           O  
ATOM   1044  CB  VAL A 172      17.352  60.710   5.339  1.00 43.09           C  
ATOM   1045  CG1 VAL A 172      17.144  61.518   4.062  1.00 44.06           C  
ATOM   1046  CG2 VAL A 172      17.773  61.622   6.492  1.00 44.13           C  
ATOM   1047  N   SER A 173      15.910  59.300   8.066  1.00 37.09           N  
ATOM   1048  CA  SER A 173      16.125  58.499   9.272  1.00 36.04           C  
ATOM   1049  C   SER A 173      15.106  57.376   9.400  1.00 36.99           C  
ATOM   1050  O   SER A 173      15.480  56.216   9.536  1.00 37.83           O  
ATOM   1051  CB  SER A 173      16.064  59.370  10.532  1.00 35.74           C  
ATOM   1052  OG  SER A 173      17.057  60.381  10.516  1.00 34.77           O  
ATOM   1053  N   PHE A 174      13.821  57.720   9.366  1.00 37.39           N  
ATOM   1054  CA  PHE A 174      12.760  56.742   9.657  1.00 38.07           C  
ATOM   1055  C   PHE A 174      12.470  55.788   8.499  1.00 38.99           C  
ATOM   1056  O   PHE A 174      12.263  54.598   8.727  1.00 39.91           O  
ATOM   1057  CB  PHE A 174      11.461  57.426  10.116  1.00 37.65           C  
ATOM   1058  CG  PHE A 174      11.406  57.687  11.594  1.00 37.33           C  
ATOM   1059  CD1 PHE A 174      11.994  58.822  12.140  1.00 38.18           C  
ATOM   1060  CD2 PHE A 174      10.763  56.790  12.448  1.00 37.55           C  
ATOM   1061  CE1 PHE A 174      11.945  59.058  13.512  1.00 38.40           C  
ATOM   1062  CE2 PHE A 174      10.707  57.020  13.816  1.00 37.21           C  
ATOM   1063  CZ  PHE A 174      11.302  58.154  14.350  1.00 38.08           C  
ATOM   1064  N   LEU A 175      12.453  56.293   7.268  1.00 39.18           N  
ATOM   1065  CA  LEU A 175      12.088  55.457   6.124  1.00 39.36           C  
ATOM   1066  C   LEU A 175      12.959  54.195   6.016  1.00 38.65           C  
ATOM   1067  O   LEU A 175      12.407  53.086   6.021  1.00 35.80           O  
ATOM   1068  CB  LEU A 175      12.076  56.262   4.811  1.00 41.71           C  
ATOM   1069  CG  LEU A 175      11.848  55.517   3.496  1.00 43.17           C  
ATOM   1070  CD1 LEU A 175      10.471  54.875   3.489  1.00 44.39           C  
ATOM   1071  CD2 LEU A 175      12.002  56.479   2.329  1.00 44.72           C  
ATOM   1072  N   PRO A 176      14.312  54.348   5.948  1.00 37.51           N  
ATOM   1073  CA  PRO A 176      15.149  53.146   5.803  1.00 35.68           C  
ATOM   1074  C   PRO A 176      15.041  52.143   6.959  1.00 35.12           C  
ATOM   1075  O   PRO A 176      15.159  50.942   6.727  1.00 32.43           O  
ATOM   1076  CB  PRO A 176      16.571  53.717   5.709  1.00 35.82           C  
ATOM   1077  CG  PRO A 176      16.382  55.113   5.237  1.00 36.06           C  
ATOM   1078  CD  PRO A 176      15.149  55.563   5.955  1.00 36.57           C  
ATOM   1079  N   ILE A 177      14.794  52.637   8.174  1.00 36.53           N  
ATOM   1080  CA  ILE A 177      14.645  51.781   9.355  1.00 37.96           C  
ATOM   1081  C   ILE A 177      13.319  51.015   9.287  1.00 40.71           C  
ATOM   1082  O   ILE A 177      13.297  49.803   9.517  1.00 40.82           O  
ATOM   1083  CB  ILE A 177      14.743  52.583  10.677  1.00 38.08           C  
ATOM   1084  CG1 ILE A 177      16.065  53.365  10.763  1.00 38.10           C  
ATOM   1085  CG2 ILE A 177      14.594  51.667  11.894  1.00 37.98           C  
ATOM   1086  CD1 ILE A 177      17.320  52.528  10.791  1.00 38.70           C  
ATOM   1087  N   MET A 178      12.233  51.725   8.968  1.00 44.60           N  
ATOM   1088  CA  MET A 178      10.915  51.114   8.715  1.00 48.06           C  
ATOM   1089  C   MET A 178      10.963  50.023   7.645  1.00 47.53           C  
ATOM   1090  O   MET A 178      10.432  48.932   7.853  1.00 47.59           O  
ATOM   1091  CB  MET A 178       9.892  52.174   8.279  1.00 52.55           C  
ATOM   1092  CG  MET A 178       9.307  53.000   9.412  1.00 56.57           C  
ATOM   1093  SD  MET A 178       8.510  54.518   8.838  1.00 65.25           S  
ATOM   1094  CE  MET A 178       7.376  53.912   7.583  1.00 63.22           C  
ATOM   1095  N   MET A 179      11.610  50.325   6.518  1.00 46.41           N  
ATOM   1096  CA  MET A 179      11.688  49.407   5.368  1.00 46.81           C  
ATOM   1097  C   MET A 179      12.689  48.247   5.498  1.00 45.10           C  
ATOM   1098  O   MET A 179      12.759  47.410   4.598  1.00 45.59           O  
ATOM   1099  CB  MET A 179      12.022  50.194   4.088  1.00 49.57           C  
ATOM   1100  CG  MET A 179      11.002  51.255   3.692  1.00 52.13           C  
ATOM   1101  SD  MET A 179       9.482  50.558   3.025  1.00 54.91           S  
ATOM   1102  CE  MET A 179       8.441  50.492   4.487  1.00 54.53           C  
ATOM   1103  N   HIS A 180      13.460  48.198   6.586  1.00 44.10           N  
ATOM   1104  CA  HIS A 180      14.501  47.171   6.801  1.00 43.80           C  
ATOM   1105  C   HIS A 180      15.628  47.173   5.750  1.00 41.04           C  
ATOM   1106  O   HIS A 180      16.274  46.150   5.528  1.00 41.74           O  
ATOM   1107  CB  HIS A 180      13.888  45.762   6.948  1.00 45.53           C  
ATOM   1108  CG  HIS A 180      13.001  45.609   8.145  1.00 47.74           C  
ATOM   1109  ND1 HIS A 180      11.928  44.746   8.169  1.00 50.39           N  
ATOM   1110  CD2 HIS A 180      13.029  46.208   9.360  1.00 48.51           C  
ATOM   1111  CE1 HIS A 180      11.335  44.815   9.349  1.00 50.16           C  
ATOM   1112  NE2 HIS A 180      11.982  45.698  10.089  1.00 48.77           N  
ATOM   1113  N   TRP A 181      15.889  48.333   5.148  1.00 38.29           N  
ATOM   1114  CA  TRP A 181      16.994  48.502   4.194  1.00 37.53           C  
ATOM   1115  C   TRP A 181      18.377  48.313   4.835  1.00 35.54           C  
ATOM   1116  O   TRP A 181      19.360  48.039   4.156  1.00 34.94           O  
ATOM   1117  CB  TRP A 181      16.927  49.900   3.562  1.00 39.72           C  
ATOM   1118  CG  TRP A 181      15.767  50.131   2.621  1.00 40.47           C  
ATOM   1119  CD1 TRP A 181      14.908  49.193   2.110  1.00 41.46           C  
ATOM   1120  CD2 TRP A 181      15.371  51.383   2.054  1.00 40.86           C  
ATOM   1121  NE1 TRP A 181      13.996  49.790   1.277  1.00 41.74           N  
ATOM   1122  CE2 TRP A 181      14.259  51.132   1.219  1.00 42.03           C  
ATOM   1123  CE3 TRP A 181      15.850  52.692   2.166  1.00 41.48           C  
ATOM   1124  CZ2 TRP A 181      13.610  52.149   0.503  1.00 43.38           C  
ATOM   1125  CZ3 TRP A 181      15.205  53.706   1.453  1.00 43.44           C  
ATOM   1126  CH2 TRP A 181      14.094  53.425   0.634  1.00 43.79           C  
ATOM   1127  N   TRP A 182      18.429  48.485   6.148  1.00 35.05           N  
ATOM   1128  CA  TRP A 182      19.645  48.347   6.954  1.00 34.40           C  
ATOM   1129  C   TRP A 182      20.087  46.915   7.251  1.00 34.72           C  
ATOM   1130  O   TRP A 182      21.255  46.702   7.548  1.00 35.16           O  
ATOM   1131  CB  TRP A 182      19.493  49.111   8.284  1.00 34.78           C  
ATOM   1132  CG  TRP A 182      18.307  48.692   9.107  1.00 34.58           C  
ATOM   1133  CD1 TRP A 182      17.013  49.071   8.925  1.00 34.55           C  
ATOM   1134  CD2 TRP A 182      18.310  47.813  10.232  1.00 35.33           C  
ATOM   1135  NE1 TRP A 182      16.204  48.480   9.857  1.00 35.41           N  
ATOM   1136  CE2 TRP A 182      16.974  47.703  10.678  1.00 35.28           C  
ATOM   1137  CE3 TRP A 182      19.310  47.105  10.911  1.00 35.96           C  
ATOM   1138  CZ2 TRP A 182      16.610  46.917  11.772  1.00 35.61           C  
ATOM   1139  CZ3 TRP A 182      18.947  46.322  12.011  1.00 36.18           C  
ATOM   1140  CH2 TRP A 182      17.609  46.237  12.426  1.00 36.11           C  
ATOM   1141  N   ARG A 183      19.190  45.938   7.153  1.00 35.74           N  
ATOM   1142  CA  ARG A 183      19.488  44.592   7.649  1.00 38.25           C  
ATOM   1143  C   ARG A 183      20.606  43.876   6.878  1.00 38.25           C  
ATOM   1144  O   ARG A 183      20.765  44.056   5.668  1.00 37.09           O  
ATOM   1145  CB  ARG A 183      18.221  43.729   7.698  1.00 40.89           C  
ATOM   1146  CG  ARG A 183      17.168  44.298   8.641  1.00 43.19           C  
ATOM   1147  CD  ARG A 183      16.154  43.278   9.134  1.00 44.94           C  
ATOM   1148  NE  ARG A 183      15.390  43.837  10.250  1.00 47.37           N  
ATOM   1149  CZ  ARG A 183      14.549  43.160  11.035  1.00 48.79           C  
ATOM   1150  NH1 ARG A 183      14.314  41.864  10.842  1.00 49.10           N  
ATOM   1151  NH2 ARG A 183      13.927  43.799  12.028  1.00 51.05           N  
ATOM   1152  N   ASP A 184      21.388  43.100   7.626  1.00 38.92           N  
ATOM   1153  CA  ASP A 184      22.485  42.291   7.117  1.00 41.04           C  
ATOM   1154  C   ASP A 184      21.983  40.849   7.059  1.00 40.94           C  
ATOM   1155  O   ASP A 184      21.000  40.515   7.709  1.00 39.76           O  
ATOM   1156  CB  ASP A 184      23.688  42.421   8.061  1.00 43.37           C  
ATOM   1157  CG  ASP A 184      24.972  41.874   7.466  1.00 45.29           C  
ATOM   1158  OD1 ASP A 184      25.386  42.391   6.406  1.00 46.13           O  
ATOM   1159  OD2 ASP A 184      25.565  40.940   8.062  1.00 45.51           O  
ATOM   1160  N   GLU A 185      22.648  40.005   6.275  1.00 43.21           N  
ATOM   1161  CA  GLU A 185      22.186  38.632   6.001  1.00 45.58           C  
ATOM   1162  C   GLU A 185      22.968  37.572   6.816  1.00 43.50           C  
ATOM   1163  O   GLU A 185      22.662  36.380   6.743  1.00 42.14           O  
ATOM   1164  CB  GLU A 185      22.317  38.359   4.486  1.00 49.16           C  
ATOM   1165  CG  GLU A 185      21.162  37.659   3.747  1.00 52.76           C  
ATOM   1166  CD  GLU A 185      20.438  36.553   4.511  1.00 56.45           C  
ATOM   1167  OE1 GLU A 185      19.461  36.863   5.230  1.00 58.47           O  
ATOM   1168  OE2 GLU A 185      20.798  35.364   4.346  1.00 57.99           O  
ATOM   1169  N   ASP A 186      23.962  38.006   7.594  1.00 42.54           N  
ATOM   1170  CA  ASP A 186      24.799  37.094   8.379  1.00 42.61           C  
ATOM   1171  C   ASP A 186      23.967  36.392   9.463  1.00 41.39           C  
ATOM   1172  O   ASP A 186      23.043  37.003   9.992  1.00 39.90           O  
ATOM   1173  CB  ASP A 186      25.949  37.865   9.029  1.00 43.97           C  
ATOM   1174  CG  ASP A 186      26.963  36.954   9.681  1.00 46.94           C  
ATOM   1175  OD1 ASP A 186      27.845  36.412   8.968  1.00 47.97           O  
ATOM   1176  OD2 ASP A 186      26.868  36.765  10.913  1.00 48.56           O  
ATOM   1177  N   PRO A 187      24.276  35.110   9.780  1.00 41.90           N  
ATOM   1178  CA  PRO A 187      23.566  34.398  10.860  1.00 42.25           C  
ATOM   1179  C   PRO A 187      23.545  35.109  12.213  1.00 42.42           C  
ATOM   1180  O   PRO A 187      22.514  35.099  12.886  1.00 43.12           O  
ATOM   1181  CB  PRO A 187      24.341  33.085  10.979  1.00 42.48           C  
ATOM   1182  CG  PRO A 187      24.865  32.844   9.615  1.00 42.13           C  
ATOM   1183  CD  PRO A 187      25.143  34.190   9.014  1.00 41.58           C  
ATOM   1184  N   GLN A 188      24.672  35.703  12.600  1.00 43.22           N  
ATOM   1185  CA  GLN A 188      24.745  36.548  13.799  1.00 44.53           C  
ATOM   1186  C   GLN A 188      23.684  37.636  13.737  1.00 41.15           C  
ATOM   1187  O   GLN A 188      22.911  37.808  14.680  1.00 40.88           O  
ATOM   1188  CB  GLN A 188      26.130  37.208  13.924  1.00 47.52           C  
ATOM   1189  CG  GLN A 188      26.349  38.021  15.199  1.00 50.91           C  
ATOM   1190  CD  GLN A 188      27.340  39.158  15.008  1.00 54.55           C  
ATOM   1191  OE1 GLN A 188      28.558  38.950  15.016  1.00 59.03           O  
ATOM   1192  NE2 GLN A 188      26.823  40.371  14.840  1.00 55.25           N  
ATOM   1193  N   ALA A 189      23.670  38.366  12.623  1.00 38.70           N  
ATOM   1194  CA  ALA A 189      22.722  39.455  12.405  1.00 36.65           C  
ATOM   1195  C   ALA A 189      21.284  38.951  12.435  1.00 35.86           C  
ATOM   1196  O   ALA A 189      20.430  39.554  13.083  1.00 33.80           O  
ATOM   1197  CB  ALA A 189      23.006  40.162  11.086  1.00 35.74           C  
ATOM   1198  N   LEU A 190      21.031  37.842  11.743  1.00 35.95           N  
ATOM   1199  CA  LEU A 190      19.687  37.266  11.662  1.00 36.79           C  
ATOM   1200  C   LEU A 190      19.178  36.802  13.027  1.00 37.19           C  
ATOM   1201  O   LEU A 190      17.999  36.982  13.335  1.00 36.40           O  
ATOM   1202  CB  LEU A 190      19.641  36.109  10.651  1.00 36.94           C  
ATOM   1203  CG  LEU A 190      19.874  36.462   9.174  1.00 37.28           C  
ATOM   1204  CD1 LEU A 190      19.968  35.187   8.345  1.00 37.29           C  
ATOM   1205  CD2 LEU A 190      18.798  37.396   8.632  1.00 37.18           C  
ATOM   1206  N   LYS A 191      20.069  36.226  13.833  1.00 37.74           N  
ATOM   1207  CA  LYS A 191      19.749  35.815  15.206  1.00 39.23           C  
ATOM   1208  C   LYS A 191      19.372  37.014  16.083  1.00 38.38           C  
ATOM   1209  O   LYS A 191      18.450  36.930  16.898  1.00 38.00           O  
ATOM   1210  CB  LYS A 191      20.929  35.063  15.836  1.00 41.93           C  
ATOM   1211  CG  LYS A 191      20.572  34.287  17.095  1.00 45.75           C  
ATOM   1212  CD  LYS A 191      21.819  33.860  17.858  1.00 49.59           C  
ATOM   1213  CE  LYS A 191      21.473  32.994  19.063  1.00 52.20           C  
ATOM   1214  NZ  LYS A 191      20.598  33.704  20.042  1.00 54.17           N  
ATOM   1215  N   CYS A 192      20.095  38.120  15.918  1.00 36.66           N  
ATOM   1216  CA  CYS A 192      19.772  39.365  16.611  1.00 34.83           C  
ATOM   1217  C   CYS A 192      18.400  39.902  16.200  1.00 34.87           C  
ATOM   1218  O   CYS A 192      17.677  40.442  17.040  1.00 34.56           O  
ATOM   1219  CB  CYS A 192      20.855  40.414  16.353  1.00 34.29           C  
ATOM   1220  SG  CYS A 192      20.618  41.975  17.228  1.00 35.31           S  
ATOM   1221  N   TYR A 193      18.042  39.746  14.922  1.00 34.83           N  
ATOM   1222  CA  TYR A 193      16.741  40.195  14.402  1.00 35.04           C  
ATOM   1223  C   TYR A 193      15.590  39.306  14.867  1.00 36.43           C  
ATOM   1224  O   TYR A 193      14.491  39.800  15.088  1.00 36.66           O  
ATOM   1225  CB  TYR A 193      16.732  40.300  12.864  1.00 34.23           C  
ATOM   1226  CG  TYR A 193      17.884  41.084  12.262  1.00 34.24           C  
ATOM   1227  CD1 TYR A 193      18.497  42.154  12.955  1.00 35.10           C  
ATOM   1228  CD2 TYR A 193      18.369  40.767  10.991  1.00 34.23           C  
ATOM   1229  CE1 TYR A 193      19.562  42.860  12.402  1.00 34.36           C  
ATOM   1230  CE2 TYR A 193      19.429  41.471  10.430  1.00 34.08           C  
ATOM   1231  CZ  TYR A 193      20.026  42.514  11.133  1.00 34.08           C  
ATOM   1232  OH  TYR A 193      21.075  43.207  10.572  1.00 31.18           O  
ATOM   1233  N   GLN A 194      15.841  38.005  15.002  1.00 39.18           N  
ATOM   1234  CA  GLN A 194      14.860  37.070  15.574  1.00 41.72           C  
ATOM   1235  C   GLN A 194      14.653  37.257  17.082  1.00 40.43           C  
ATOM   1236  O   GLN A 194      13.605  36.894  17.613  1.00 40.53           O  
ATOM   1237  CB  GLN A 194      15.287  35.622  15.321  1.00 45.13           C  
ATOM   1238  CG  GLN A 194      15.206  35.192  13.863  1.00 48.57           C  
ATOM   1239  CD  GLN A 194      16.036  33.949  13.579  1.00 52.57           C  
ATOM   1240  OE1 GLN A 194      16.289  33.135  14.476  1.00 54.73           O  
ATOM   1241  NE2 GLN A 194      16.471  33.799  12.329  1.00 54.02           N  
ATOM   1242  N   ASP A 195      15.665  37.787  17.759  1.00 38.30           N  
ATOM   1243  CA  ASP A 195      15.645  37.971  19.199  1.00 38.15           C  
ATOM   1244  C   ASP A 195      15.144  39.385  19.556  1.00 38.70           C  
ATOM   1245  O   ASP A 195      15.838  40.381  19.284  1.00 37.72           O  
ATOM   1246  CB  ASP A 195      17.061  37.745  19.744  1.00 37.69           C  
ATOM   1247  CG  ASP A 195      17.110  37.614  21.245  1.00 38.28           C  
ATOM   1248  OD1 ASP A 195      16.059  37.674  21.930  1.00 38.86           O  
ATOM   1249  OD2 ASP A 195      18.234  37.446  21.751  1.00 40.87           O  
ATOM   1250  N   PRO A 196      13.939  39.493  20.158  1.00 39.07           N  
ATOM   1251  CA  PRO A 196      13.551  40.803  20.727  1.00 37.98           C  
ATOM   1252  C   PRO A 196      14.494  41.336  21.828  1.00 35.61           C  
ATOM   1253  O   PRO A 196      14.486  42.536  22.100  1.00 34.60           O  
ATOM   1254  CB  PRO A 196      12.136  40.556  21.282  1.00 39.03           C  
ATOM   1255  CG  PRO A 196      11.888  39.084  21.167  1.00 39.77           C  
ATOM   1256  CD  PRO A 196      12.796  38.564  20.103  1.00 39.21           C  
ATOM   1257  N   GLY A 197      15.285  40.452  22.442  1.00 33.08           N  
ATOM   1258  CA  GLY A 197      16.302  40.835  23.417  1.00 32.53           C  
ATOM   1259  C   GLY A 197      17.593  41.428  22.883  1.00 32.51           C  
ATOM   1260  O   GLY A 197      18.389  41.942  23.663  1.00 32.44           O  
ATOM   1261  N   CYS A 198      17.814  41.347  21.571  1.00 33.03           N  
ATOM   1262  CA  CYS A 198      18.980  41.949  20.928  1.00 32.81           C  
ATOM   1263  C   CYS A 198      18.581  43.220  20.185  1.00 31.30           C  
ATOM   1264  O   CYS A 198      17.739  43.162  19.288  1.00 30.54           O  
ATOM   1265  CB  CYS A 198      19.607  40.962  19.945  1.00 33.10           C  
ATOM   1266  SG  CYS A 198      21.128  41.573  19.180  1.00 35.18           S  
ATOM   1267  N   CYS A 199      19.181  44.352  20.555  1.00 30.58           N  
ATOM   1268  CA  CYS A 199      19.003  45.617  19.833  1.00 30.85           C  
ATOM   1269  C   CYS A 199      20.359  46.214  19.423  1.00 32.31           C  
ATOM   1270  O   CYS A 199      20.614  47.403  19.605  1.00 33.49           O  
ATOM   1271  CB  CYS A 199      18.187  46.607  20.682  1.00 29.54           C  
ATOM   1272  SG  CYS A 199      17.531  48.031  19.778  1.00 27.72           S  
ATOM   1273  N   ASP A 200      21.231  45.371  18.875  1.00 34.34           N  
ATOM   1274  CA  ASP A 200      22.464  45.836  18.224  1.00 34.98           C  
ATOM   1275  C   ASP A 200      22.108  46.266  16.816  1.00 32.20           C  
ATOM   1276  O   ASP A 200      21.498  45.505  16.062  1.00 31.55           O  
ATOM   1277  CB  ASP A 200      23.527  44.730  18.152  1.00 37.13           C  
ATOM   1278  CG  ASP A 200      24.054  44.326  19.516  1.00 39.95           C  
ATOM   1279  OD1 ASP A 200      23.609  44.883  20.545  1.00 42.59           O  
ATOM   1280  OD2 ASP A 200      24.928  43.439  19.561  1.00 43.45           O  
ATOM   1281  N   PHE A 201      22.503  47.482  16.459  1.00 30.88           N  
ATOM   1282  CA  PHE A 201      22.246  48.030  15.134  1.00 29.57           C  
ATOM   1283  C   PHE A 201      23.281  47.448  14.162  1.00 29.15           C  
ATOM   1284  O   PHE A 201      24.192  48.147  13.714  1.00 29.06           O  
ATOM   1285  CB  PHE A 201      22.274  49.574  15.202  1.00 28.66           C  
ATOM   1286  CG  PHE A 201      21.643  50.276  14.019  1.00 28.86           C  
ATOM   1287  CD1 PHE A 201      20.482  49.793  13.402  1.00 28.74           C  
ATOM   1288  CD2 PHE A 201      22.188  51.471  13.551  1.00 29.02           C  
ATOM   1289  CE1 PHE A 201      19.910  50.469  12.332  1.00 28.91           C  
ATOM   1290  CE2 PHE A 201      21.616  52.148  12.482  1.00 29.02           C  
ATOM   1291  CZ  PHE A 201      20.474  51.649  11.875  1.00 28.77           C  
ATOM   1292  N   VAL A 202      23.119  46.153  13.867  1.00 28.01           N  
ATOM   1293  CA  VAL A 202      23.971  45.419  12.937  1.00 28.04           C  
ATOM   1294  C   VAL A 202      23.438  45.722  11.540  1.00 27.43           C  
ATOM   1295  O   VAL A 202      22.270  45.456  11.235  1.00 27.24           O  
ATOM   1296  CB  VAL A 202      23.924  43.886  13.169  1.00 29.06           C  
ATOM   1297  CG1 VAL A 202      24.876  43.168  12.217  1.00 29.54           C  
ATOM   1298  CG2 VAL A 202      24.270  43.537  14.606  1.00 29.34           C  
ATOM   1299  N   THR A 203      24.284  46.299  10.699  1.00 26.49           N  
ATOM   1300  CA  THR A 203      23.840  46.806   9.411  1.00 26.76           C  
ATOM   1301  C   THR A 203      24.692  46.242   8.295  1.00 25.79           C  
ATOM   1302  O   THR A 203      25.843  45.872   8.513  1.00 25.62           O  
ATOM   1303  CB  THR A 203      23.886  48.351   9.358  1.00 26.68           C  
ATOM   1304  OG1 THR A 203      25.242  48.808   9.454  1.00 27.21           O  
ATOM   1305  CG2 THR A 203      23.083  48.953  10.499  1.00 26.70           C  
ATOM   1306  N   ASN A 204      24.106  46.167   7.106  1.00 25.40           N  
ATOM   1307  CA  ASN A 204      24.867  45.915   5.887  1.00 24.61           C  
ATOM   1308  C   ASN A 204      25.698  47.156   5.521  1.00 25.19           C  
ATOM   1309  O   ASN A 204      25.349  48.283   5.872  1.00 24.30           O  
ATOM   1310  CB  ASN A 204      23.936  45.477   4.741  1.00 24.55           C  
ATOM   1311  CG  ASN A 204      22.980  46.571   4.296  1.00 24.81           C  
ATOM   1312  OD1 ASN A 204      23.407  47.592   3.764  1.00 26.28           O  
ATOM   1313  ND2 ASN A 204      21.681  46.354   4.481  1.00 24.87           N  
ATOM   1314  N   ARG A 205      26.825  46.916   4.864  1.00 26.56           N  
ATOM   1315  CA  ARG A 205      27.753  47.945   4.387  1.00 27.28           C  
ATOM   1316  C   ARG A 205      27.142  49.020   3.487  1.00 25.39           C  
ATOM   1317  O   ARG A 205      27.525  50.186   3.582  1.00 24.84           O  
ATOM   1318  CB  ARG A 205      28.925  47.294   3.644  1.00 30.29           C  
ATOM   1319  CG  ARG A 205      29.813  46.392   4.488  1.00 34.05           C  
ATOM   1320  CD  ARG A 205      30.775  45.610   3.606  1.00 38.75           C  
ATOM   1321  NE  ARG A 205      31.481  44.544   4.325  1.00 42.95           N  
ATOM   1322  CZ  ARG A 205      32.555  43.888   3.868  1.00 46.92           C  
ATOM   1323  NH1 ARG A 205      33.087  44.169   2.671  1.00 48.37           N  
ATOM   1324  NH2 ARG A 205      33.115  42.941   4.621  1.00 48.38           N  
ATOM   1325  N   ALA A 206      26.220  48.634   2.608  1.00 24.86           N  
ATOM   1326  CA  ALA A 206      25.564  49.598   1.710  1.00 24.73           C  
ATOM   1327  C   ALA A 206      24.820  50.677   2.490  1.00 23.94           C  
ATOM   1328  O   ALA A 206      25.001  51.872   2.240  1.00 22.53           O  
ATOM   1329  CB  ALA A 206      24.610  48.896   0.753  1.00 24.89           C  
ATOM   1330  N   TYR A 207      23.994  50.240   3.440  1.00 23.77           N  
ATOM   1331  CA  TYR A 207      23.265  51.161   4.311  1.00 23.89           C  
ATOM   1332  C   TYR A 207      24.206  52.004   5.182  1.00 23.13           C  
ATOM   1333  O   TYR A 207      24.026  53.222   5.294  1.00 23.40           O  
ATOM   1334  CB  TYR A 207      22.265  50.424   5.207  1.00 24.35           C  
ATOM   1335  CG  TYR A 207      21.715  51.324   6.282  1.00 25.02           C  
ATOM   1336  CD1 TYR A 207      20.682  52.212   6.011  1.00 25.83           C  
ATOM   1337  CD2 TYR A 207      22.267  51.330   7.561  1.00 25.50           C  
ATOM   1338  CE1 TYR A 207      20.193  53.065   6.991  1.00 26.22           C  
ATOM   1339  CE2 TYR A 207      21.788  52.176   8.547  1.00 25.63           C  
ATOM   1340  CZ  TYR A 207      20.754  53.045   8.261  1.00 25.97           C  
ATOM   1341  OH  TYR A 207      20.281  53.887   9.245  1.00 26.56           O  
ATOM   1342  N   ALA A 208      25.190  51.355   5.796  1.00 21.60           N  
ATOM   1343  CA  ALA A 208      26.129  52.037   6.686  1.00 21.18           C  
ATOM   1344  C   ALA A 208      26.890  53.166   6.011  1.00 20.77           C  
ATOM   1345  O   ALA A 208      26.981  54.259   6.559  1.00 20.11           O  
ATOM   1346  CB  ALA A 208      27.117  51.042   7.275  1.00 21.30           C  
ATOM   1347  N   ILE A 209      27.441  52.891   4.829  1.00 20.57           N  
ATOM   1348  CA  ILE A 209      28.210  53.885   4.086  1.00 20.62           C  
ATOM   1349  C   ILE A 209      27.285  54.994   3.597  1.00 20.06           C  
ATOM   1350  O   ILE A 209      27.566  56.173   3.809  1.00 20.26           O  
ATOM   1351  CB  ILE A 209      28.999  53.245   2.907  1.00 21.45           C  
ATOM   1352  CG1 ILE A 209      30.104  52.331   3.444  1.00 21.98           C  
ATOM   1353  CG2 ILE A 209      29.633  54.312   2.018  1.00 21.24           C  
ATOM   1354  CD1 ILE A 209      30.538  51.262   2.468  1.00 22.70           C  
ATOM   1355  N   ALA A 210      26.178  54.613   2.966  1.00 19.70           N  
ATOM   1356  CA  ALA A 210      25.244  55.583   2.390  1.00 19.59           C  
ATOM   1357  C   ALA A 210      24.572  56.468   3.434  1.00 19.55           C  
ATOM   1358  O   ALA A 210      24.510  57.679   3.259  1.00 19.55           O  
ATOM   1359  CB  ALA A 210      24.195  54.877   1.548  1.00 19.77           C  
ATOM   1360  N   SER A 211      24.081  55.877   4.520  1.00 19.78           N  
ATOM   1361  CA  SER A 211      23.435  56.662   5.586  1.00 20.09           C  
ATOM   1362  C   SER A 211      24.418  57.626   6.259  1.00 20.17           C  
ATOM   1363  O   SER A 211      24.091  58.790   6.482  1.00 20.03           O  
ATOM   1364  CB  SER A 211      22.815  55.747   6.636  1.00 20.17           C  
ATOM   1365  OG  SER A 211      23.815  55.027   7.328  1.00 20.37           O  
ATOM   1366  N   SER A 212      25.619  57.130   6.565  1.00 20.21           N  
ATOM   1367  CA  SER A 212      26.698  57.953   7.136  1.00 20.27           C  
ATOM   1368  C   SER A 212      27.123  59.128   6.269  1.00 20.61           C  
ATOM   1369  O   SER A 212      27.473  60.179   6.798  1.00 20.63           O  
ATOM   1370  CB  SER A 212      27.927  57.098   7.416  1.00 20.10           C  
ATOM   1371  OG  SER A 212      27.628  56.155   8.415  1.00 21.11           O  
ATOM   1372  N   ILE A 213      27.121  58.938   4.950  1.00 21.44           N  
ATOM   1373  CA  ILE A 213      27.448  60.006   4.010  1.00 22.13           C  
ATOM   1374  C   ILE A 213      26.377  61.104   4.024  1.00 22.40           C  
ATOM   1375  O   ILE A 213      26.681  62.277   4.207  1.00 21.79           O  
ATOM   1376  CB  ILE A 213      27.649  59.451   2.576  1.00 22.70           C  
ATOM   1377  CG1 ILE A 213      28.994  58.723   2.474  1.00 23.05           C  
ATOM   1378  CG2 ILE A 213      27.622  60.571   1.536  1.00 23.14           C  
ATOM   1379  CD1 ILE A 213      29.060  57.714   1.342  1.00 23.42           C  
ATOM   1380  N   ILE A 214      25.131  60.700   3.811  1.00 23.92           N  
ATOM   1381  CA  ILE A 214      23.993  61.620   3.731  1.00 25.17           C  
ATOM   1382  C   ILE A 214      23.716  62.322   5.060  1.00 25.00           C  
ATOM   1383  O   ILE A 214      23.394  63.508   5.075  1.00 24.93           O  
ATOM   1384  CB  ILE A 214      22.712  60.875   3.249  1.00 26.74           C  
ATOM   1385  CG1 ILE A 214      22.832  60.555   1.759  1.00 27.60           C  
ATOM   1386  CG2 ILE A 214      21.437  61.687   3.508  1.00 27.45           C  
ATOM   1387  CD1 ILE A 214      21.694  59.710   1.213  1.00 28.75           C  
ATOM   1388  N   SER A 215      23.818  61.587   6.164  1.00 24.97           N  
ATOM   1389  CA  SER A 215      23.424  62.115   7.472  1.00 25.11           C  
ATOM   1390  C   SER A 215      24.546  62.718   8.295  1.00 24.43           C  
ATOM   1391  O   SER A 215      24.247  63.365   9.285  1.00 24.70           O  
ATOM   1392  CB  SER A 215      22.743  61.031   8.305  1.00 25.55           C  
ATOM   1393  OG  SER A 215      21.472  60.692   7.776  1.00 26.55           O  
ATOM   1394  N   PHE A 216      25.812  62.514   7.915  1.00 23.90           N  
ATOM   1395  CA  PHE A 216      26.942  62.991   8.723  1.00 23.49           C  
ATOM   1396  C   PHE A 216      28.103  63.574   7.905  1.00 23.61           C  
ATOM   1397  O   PHE A 216      28.392  64.767   8.019  1.00 22.94           O  
ATOM   1398  CB  PHE A 216      27.443  61.877   9.660  1.00 23.25           C  
ATOM   1399  CG  PHE A 216      28.590  62.297  10.538  1.00 22.49           C  
ATOM   1400  CD1 PHE A 216      28.369  63.117  11.647  1.00 22.35           C  
ATOM   1401  CD2 PHE A 216      29.891  61.900  10.247  1.00 21.80           C  
ATOM   1402  CE1 PHE A 216      29.426  63.521  12.449  1.00 21.92           C  
ATOM   1403  CE2 PHE A 216      30.950  62.301  11.047  1.00 21.75           C  
ATOM   1404  CZ  PHE A 216      30.717  63.111  12.151  1.00 21.69           C  
ATOM   1405  N   TYR A 217      28.764  62.755   7.091  1.00 24.27           N  
ATOM   1406  CA  TYR A 217      30.003  63.197   6.412  1.00 25.26           C  
ATOM   1407  C   TYR A 217      29.818  64.412   5.502  1.00 26.33           C  
ATOM   1408  O   TYR A 217      30.636  65.328   5.537  1.00 26.56           O  
ATOM   1409  CB  TYR A 217      30.673  62.063   5.627  1.00 24.85           C  
ATOM   1410  CG  TYR A 217      31.314  61.016   6.506  1.00 25.30           C  
ATOM   1411  CD1 TYR A 217      32.439  61.324   7.282  1.00 25.79           C  
ATOM   1412  CD2 TYR A 217      30.813  59.713   6.561  1.00 25.24           C  
ATOM   1413  CE1 TYR A 217      33.037  60.371   8.098  1.00 25.94           C  
ATOM   1414  CE2 TYR A 217      31.409  58.751   7.366  1.00 26.23           C  
ATOM   1415  CZ  TYR A 217      32.519  59.085   8.135  1.00 26.55           C  
ATOM   1416  OH  TYR A 217      33.108  58.136   8.939  1.00 27.85           O  
ATOM   1417  N   ILE A 218      28.760  64.419   4.693  1.00 27.08           N  
ATOM   1418  CA  ILE A 218      28.485  65.565   3.816  1.00 27.77           C  
ATOM   1419  C   ILE A 218      28.161  66.836   4.604  1.00 26.32           C  
ATOM   1420  O   ILE A 218      28.801  67.867   4.379  1.00 26.35           O  
ATOM   1421  CB  ILE A 218      27.382  65.257   2.762  1.00 29.05           C  
ATOM   1422  CG1 ILE A 218      27.901  64.223   1.752  1.00 30.19           C  
ATOM   1423  CG2 ILE A 218      26.913  66.522   2.037  1.00 29.00           C  
ATOM   1424  CD1 ILE A 218      29.231  64.557   1.104  1.00 30.57           C  
ATOM   1425  N   PRO A 219      27.177  66.777   5.517  1.00 24.94           N  
ATOM   1426  CA  PRO A 219      26.948  68.003   6.281  1.00 24.43           C  
ATOM   1427  C   PRO A 219      28.153  68.427   7.155  1.00 24.33           C  
ATOM   1428  O   PRO A 219      28.417  69.630   7.267  1.00 23.83           O  
ATOM   1429  CB  PRO A 219      25.691  67.688   7.105  1.00 24.37           C  
ATOM   1430  CG  PRO A 219      25.553  66.206   7.082  1.00 24.50           C  
ATOM   1431  CD  PRO A 219      26.157  65.748   5.795  1.00 24.43           C  
ATOM   1432  N   LEU A 220      28.890  67.467   7.722  1.00 23.98           N  
ATOM   1433  CA  LEU A 220      30.103  67.793   8.498  1.00 24.73           C  
ATOM   1434  C   LEU A 220      31.165  68.524   7.670  1.00 25.33           C  
ATOM   1435  O   LEU A 220      31.737  69.510   8.145  1.00 24.69           O  
ATOM   1436  CB  LEU A 220      30.741  66.545   9.121  1.00 24.89           C  
ATOM   1437  CG  LEU A 220      31.837  66.845  10.155  1.00 25.00           C  
ATOM   1438  CD1 LEU A 220      31.206  67.227  11.484  1.00 25.45           C  
ATOM   1439  CD2 LEU A 220      32.777  65.664  10.330  1.00 25.19           C  
ATOM   1440  N   LEU A 221      31.417  68.043   6.447  1.00 25.52           N  
ATOM   1441  CA  LEU A 221      32.413  68.656   5.557  1.00 25.58           C  
ATOM   1442  C   LEU A 221      31.990  70.038   5.067  1.00 25.04           C  
ATOM   1443  O   LEU A 221      32.812  70.950   4.999  1.00 24.24           O  
ATOM   1444  CB  LEU A 221      32.732  67.743   4.373  1.00 26.48           C  
ATOM   1445  CG  LEU A 221      33.417  66.420   4.744  1.00 28.15           C  
ATOM   1446  CD1 LEU A 221      33.321  65.430   3.587  1.00 28.88           C  
ATOM   1447  CD2 LEU A 221      34.868  66.619   5.179  1.00 28.52           C  
ATOM   1448  N   ILE A 222      30.712  70.197   4.742  1.00 25.57           N  
ATOM   1449  CA  ILE A 222      30.174  71.511   4.372  1.00 25.71           C  
ATOM   1450  C   ILE A 222      30.284  72.479   5.556  1.00 25.56           C  
ATOM   1451  O   ILE A 222      30.713  73.615   5.378  1.00 26.13           O  
ATOM   1452  CB  ILE A 222      28.712  71.421   3.870  1.00 26.54           C  
ATOM   1453  CG1 ILE A 222      28.663  70.669   2.530  1.00 26.76           C  
ATOM   1454  CG2 ILE A 222      28.112  72.815   3.686  1.00 26.72           C  
ATOM   1455  CD1 ILE A 222      27.270  70.310   2.057  1.00 26.83           C  
ATOM   1456  N   MET A 223      29.904  72.022   6.751  1.00 24.98           N  
ATOM   1457  CA  MET A 223      29.988  72.836   7.978  1.00 24.61           C  
ATOM   1458  C   MET A 223      31.408  73.336   8.236  1.00 23.70           C  
ATOM   1459  O   MET A 223      31.613  74.514   8.496  1.00 22.13           O  
ATOM   1460  CB  MET A 223      29.495  72.021   9.182  1.00 24.83           C  
ATOM   1461  CG  MET A 223      29.474  72.751  10.518  1.00 25.18           C  
ATOM   1462  SD  MET A 223      29.496  71.615  11.921  1.00 26.25           S  
ATOM   1463  CE  MET A 223      31.174  70.987  11.818  1.00 26.27           C  
ATOM   1464  N   ILE A 224      32.376  72.427   8.165  1.00 24.76           N  
ATOM   1465  CA  ILE A 224      33.798  72.767   8.380  1.00 25.29           C  
ATOM   1466  C   ILE A 224      34.311  73.759   7.328  1.00 26.50           C  
ATOM   1467  O   ILE A 224      34.884  74.796   7.671  1.00 27.00           O  
ATOM   1468  CB  ILE A 224      34.682  71.496   8.404  1.00 24.43           C  
ATOM   1469  CG1 ILE A 224      34.403  70.697   9.687  1.00 24.38           C  
ATOM   1470  CG2 ILE A 224      36.167  71.843   8.323  1.00 24.28           C  
ATOM   1471  CD1 ILE A 224      34.851  69.251   9.627  1.00 24.22           C  
ATOM   1472  N   PHE A 225      34.104  73.424   6.059  1.00 27.06           N  
ATOM   1473  CA  PHE A 225      34.535  74.266   4.945  1.00 28.78           C  
ATOM   1474  C   PHE A 225      34.003  75.700   5.083  1.00 28.49           C  
ATOM   1475  O   PHE A 225      34.776  76.657   5.077  1.00 27.85           O  
ATOM   1476  CB  PHE A 225      34.076  73.629   3.627  1.00 30.73           C  
ATOM   1477  CG  PHE A 225      34.353  74.461   2.408  1.00 32.39           C  
ATOM   1478  CD1 PHE A 225      35.653  74.641   1.955  1.00 34.26           C  
ATOM   1479  CD2 PHE A 225      33.307  75.043   1.691  1.00 34.00           C  
ATOM   1480  CE1 PHE A 225      35.912  75.404   0.818  1.00 35.10           C  
ATOM   1481  CE2 PHE A 225      33.556  75.805   0.556  1.00 34.44           C  
ATOM   1482  CZ  PHE A 225      34.861  75.988   0.119  1.00 34.93           C  
ATOM   1483  N   VAL A 226      32.688  75.818   5.258  1.00 28.00           N  
ATOM   1484  CA  VAL A 226      32.007  77.104   5.359  1.00 27.55           C  
ATOM   1485  C   VAL A 226      32.400  77.853   6.633  1.00 28.22           C  
ATOM   1486  O   VAL A 226      32.652  79.060   6.578  1.00 28.89           O  
ATOM   1487  CB  VAL A 226      30.467  76.935   5.276  1.00 28.01           C  
ATOM   1488  CG1 VAL A 226      29.741  78.254   5.550  1.00 27.75           C  
ATOM   1489  CG2 VAL A 226      30.072  76.394   3.902  1.00 28.21           C  
ATOM   1490  N   ALA A 227      32.455  77.152   7.768  1.00 28.22           N  
ATOM   1491  CA  ALA A 227      32.879  77.772   9.040  1.00 28.65           C  
ATOM   1492  C   ALA A 227      34.288  78.387   8.966  1.00 28.89           C  
ATOM   1493  O   ALA A 227      34.522  79.467   9.506  1.00 28.06           O  
ATOM   1494  CB  ALA A 227      32.794  76.776  10.190  1.00 27.71           C  
ATOM   1495  N   LEU A 228      35.211  77.707   8.287  1.00 30.28           N  
ATOM   1496  CA  LEU A 228      36.576  78.221   8.113  1.00 31.42           C  
ATOM   1497  C   LEU A 228      36.593  79.503   7.299  1.00 32.85           C  
ATOM   1498  O   LEU A 228      37.377  80.407   7.588  1.00 32.85           O  
ATOM   1499  CB  LEU A 228      37.478  77.184   7.444  1.00 31.70           C  
ATOM   1500  CG  LEU A 228      37.764  75.931   8.275  1.00 32.21           C  
ATOM   1501  CD1 LEU A 228      38.254  74.797   7.377  1.00 32.63           C  
ATOM   1502  CD2 LEU A 228      38.752  76.229   9.394  1.00 31.78           C  
ATOM   1503  N   ARG A 229      35.740  79.576   6.278  1.00 35.03           N  
ATOM   1504  CA  ARG A 229      35.604  80.797   5.491  1.00 37.22           C  
ATOM   1505  C   ARG A 229      34.989  81.937   6.315  1.00 35.38           C  
ATOM   1506  O   ARG A 229      35.428  83.076   6.186  1.00 35.13           O  
ATOM   1507  CB  ARG A 229      34.793  80.558   4.208  1.00 40.45           C  
ATOM   1508  CG  ARG A 229      35.325  79.503   3.234  1.00 44.76           C  
ATOM   1509  CD  ARG A 229      36.823  79.557   2.927  1.00 50.19           C  
ATOM   1510  NE  ARG A 229      37.547  78.322   3.299  1.00 57.13           N  
ATOM   1511  CZ  ARG A 229      38.500  78.197   4.240  1.00 61.81           C  
ATOM   1512  NH1 ARG A 229      38.908  79.225   4.994  1.00 63.26           N  
ATOM   1513  NH2 ARG A 229      39.063  77.002   4.439  1.00 63.24           N  
ATOM   1514  N   VAL A 230      33.993  81.628   7.154  1.00 34.65           N  
ATOM   1515  CA  VAL A 230      33.410  82.603   8.111  1.00 34.79           C  
ATOM   1516  C   VAL A 230      34.481  83.134   9.064  1.00 34.28           C  
ATOM   1517  O   VAL A 230      34.569  84.342   9.299  1.00 31.58           O  
ATOM   1518  CB  VAL A 230      32.238  81.997   8.944  1.00 33.89           C  
ATOM   1519  CG1 VAL A 230      31.875  82.871  10.144  1.00 33.77           C  
ATOM   1520  CG2 VAL A 230      31.010  81.780   8.072  1.00 33.14           C  
ATOM   1521  N   TYR A 231      35.274  82.216   9.607  1.00 36.05           N  
ATOM   1522  CA  TYR A 231      36.408  82.559  10.467  1.00 39.68           C  
ATOM   1523  C   TYR A 231      37.345  83.514   9.742  1.00 41.25           C  
ATOM   1524  O   TYR A 231      37.691  84.569  10.277  1.00 40.08           O  
ATOM   1525  CB  TYR A 231      37.141  81.282  10.904  1.00 41.39           C  
ATOM   1526  CG  TYR A 231      38.331  81.433  11.840  1.00 45.17           C  
ATOM   1527  CD1 TYR A 231      38.560  82.598  12.588  1.00 47.12           C  
ATOM   1528  CD2 TYR A 231      39.218  80.375  12.010  1.00 48.68           C  
ATOM   1529  CE1 TYR A 231      39.649  82.704  13.439  1.00 48.12           C  
ATOM   1530  CE2 TYR A 231      40.306  80.478  12.865  1.00 50.08           C  
ATOM   1531  CZ  TYR A 231      40.514  81.643  13.577  1.00 48.82           C  
ATOM   1532  OH  TYR A 231      41.591  81.742  14.420  1.00 52.10           O  
ATOM   1533  N   ARG A 232      37.710  83.150   8.515  1.00 44.05           N  
ATOM   1534  CA  ARG A 232      38.580  83.969   7.670  1.00 46.99           C  
ATOM   1535  C   ARG A 232      38.004  85.369   7.420  1.00 45.70           C  
ATOM   1536  O   ARG A 232      38.725  86.358   7.528  1.00 44.99           O  
ATOM   1537  CB  ARG A 232      38.826  83.261   6.329  1.00 51.12           C  
ATOM   1538  CG  ARG A 232      39.938  83.864   5.475  1.00 55.15           C  
ATOM   1539  CD  ARG A 232      39.885  83.340   4.045  1.00 58.25           C  
ATOM   1540  NE  ARG A 232      40.482  82.006   3.895  1.00 61.07           N  
ATOM   1541  CZ  ARG A 232      40.188  81.124   2.931  1.00 64.62           C  
ATOM   1542  NH1 ARG A 232      39.258  81.376   2.003  1.00 64.96           N  
ATOM   1543  NH2 ARG A 232      40.818  79.949   2.907  1.00 65.58           N  
ATOM   1544  N   GLU A 233      36.713  85.437   7.095  1.00 44.22           N  
ATOM   1545  CA  GLU A 233      36.041  86.703   6.756  1.00 43.62           C  
ATOM   1546  C   GLU A 233      35.817  87.594   7.982  1.00 42.99           C  
ATOM   1547  O   GLU A 233      35.962  88.813   7.889  1.00 42.10           O  
ATOM   1548  CB  GLU A 233      34.710  86.417   6.046  1.00 45.13           C  
ATOM   1549  CG  GLU A 233      33.820  87.623   5.752  1.00 46.97           C  
ATOM   1550  CD  GLU A 233      34.422  88.604   4.759  1.00 49.38           C  
ATOM   1551  OE1 GLU A 233      34.960  88.156   3.720  1.00 51.03           O  
ATOM   1552  OE2 GLU A 233      34.326  89.828   5.003  1.00 49.24           O  
ATOM   1553  N   ALA A 234      35.437  86.995   9.110  1.00 41.83           N  
ATOM   1554  CA  ALA A 234      35.356  87.723  10.379  1.00 43.04           C  
ATOM   1555  C   ALA A 234      36.724  88.324  10.705  1.00 45.51           C  
ATOM   1556  O   ALA A 234      36.849  89.533  10.928  1.00 43.00           O  
ATOM   1557  CB  ALA A 234      34.900  86.804  11.505  1.00 42.17           C  
ATOM   1558  N   LYS A 235      37.742  87.467  10.681  1.00 47.33           N  
ATOM   1559  CA  LYS A 235      39.131  87.866  10.920  1.00 51.13           C  
ATOM   1560  C   LYS A 235      39.574  89.042  10.043  1.00 52.58           C  
ATOM   1561  O   LYS A 235      40.326  89.884  10.508  1.00 53.00           O  
ATOM   1562  CB  LYS A 235      40.067  86.673  10.705  1.00 54.42           C  
ATOM   1563  CG  LYS A 235      41.480  86.828  11.243  1.00 58.44           C  
ATOM   1564  CD  LYS A 235      42.326  85.628  10.819  1.00 62.77           C  
ATOM   1565  CE  LYS A 235      43.476  85.344  11.773  1.00 65.79           C  
ATOM   1566  NZ  LYS A 235      44.054  83.992  11.527  1.00 67.83           N  
ATOM   1567  N   GLU A 236      39.115  89.100   8.790  1.00 53.78           N  
ATOM   1568  CA  GLU A 236      39.428  90.236   7.901  1.00 53.74           C  
ATOM   1569  C   GLU A 236      38.648  91.523   8.199  1.00 54.01           C  
ATOM   1570  O   GLU A 236      39.187  92.619   8.021  1.00 52.75           O  
ATOM   1571  CB  GLU A 236      39.247  89.852   6.426  1.00 54.27           C  
ATOM   1572  CG  GLU A 236      40.294  88.884   5.890  1.00 55.94           C  
ATOM   1573  CD  GLU A 236      41.724  89.314   6.184  1.00 57.64           C  
ATOM   1574  OE1 GLU A 236      42.036  90.517   6.043  1.00 59.81           O  
ATOM   1575  OE2 GLU A 236      42.541  88.448   6.565  1.00 59.19           O  
ATOM   1576  N   GLN A 237      37.397  91.394   8.644  1.00 54.50           N  
ATOM   1577  CA  GLN A 237      36.556  92.559   8.952  1.00 54.60           C  
ATOM   1578  C   GLN A 237      37.030  93.390  10.159  1.00 56.25           C  
ATOM   1579  O   GLN A 237      36.903  94.620  10.146  1.00 57.11           O  
ATOM   1580  CB  GLN A 237      35.088  92.147   9.121  1.00 54.06           C  
ATOM   1581  CG  GLN A 237      34.394  91.869   7.795  1.00 54.24           C  
ATOM   1582  CD  GLN A 237      32.905  91.590   7.924  1.00 54.64           C  
ATOM   1583  OE1 GLN A 237      32.308  91.749   8.991  1.00 54.41           O  
ATOM   1584  NE2 GLN A 237      32.296  91.170   6.823  1.00 56.64           N  
ATOM   1585  N   ILE A 238      37.550  92.731  11.194  1.00 57.23           N  
ATOM   1586  CA  ILE A 238      38.211  93.452  12.306  1.00 61.07           C  
ATOM   1587  C   ILE A 238      39.499  94.156  11.878  1.00 63.41           C  
ATOM   1588  O   ILE A 238      39.791  95.237  12.386  1.00 65.44           O  
ATOM   1589  CB  ILE A 238      38.555  92.577  13.544  1.00 60.52           C  
ATOM   1590  CG1 ILE A 238      39.124  91.216  13.132  1.00 61.98           C  
ATOM   1591  CG2 ILE A 238      37.353  92.454  14.468  1.00 60.42           C  
ATOM   1592  CD1 ILE A 238      40.024  90.590  14.163  1.00 62.90           C  
ATOM   1593  N   ARG A 239      40.258  93.556  10.960  1.00 64.87           N  
ATOM   1594  CA  ARG A 239      41.544  94.124  10.530  1.00 67.28           C  
ATOM   1595  C   ARG A 239      41.337  95.390   9.697  1.00 66.50           C  
ATOM   1596  O   ARG A 239      42.072  96.360   9.871  1.00 67.44           O  
ATOM   1597  CB  ARG A 239      42.379  93.107   9.739  1.00 69.91           C  
ATOM   1598  CG  ARG A 239      42.731  91.835  10.498  1.00 72.78           C  
ATOM   1599  CD  ARG A 239      43.846  92.013  11.514  1.00 76.09           C  
ATOM   1600  NE  ARG A 239      43.996  90.816  12.349  1.00 79.32           N  
ATOM   1601  CZ  ARG A 239      44.578  89.674  11.972  1.00 82.87           C  
ATOM   1602  NH1 ARG A 239      45.098  89.527  10.750  1.00 85.02           N  
ATOM   1603  NH2 ARG A 239      44.647  88.657  12.830  1.00 85.42           N  
ATOM   1604  N   LYS A 240      40.327  95.375   8.819  1.00 64.69           N  
ATOM   1605  CA  LYS A 240      39.958  96.517   7.952  1.00 63.24           C  
ATOM   1606  C   LYS A 240      41.153  97.195   7.278  1.00 60.41           C  
ATOM   1607  O   LYS A 240      41.728  96.653   6.335  1.00 58.19           O  
ATOM   1608  CB  LYS A 240      39.064  97.552   8.681  1.00 63.91           C  
ATOM   1609  CG  LYS A 240      39.066  97.512  10.208  1.00 65.41           C  
ATOM   1610  CD  LYS A 240      38.076  98.493  10.817  1.00 65.68           C  
ATOM   1611  CE  LYS A 240      36.664  97.933  10.853  1.00 66.57           C  
ATOM   1612  NZ  LYS A 240      35.665  98.988  11.177  1.00 66.81           N  
ATOM   1613  N   ARG A 275      33.261  97.093   6.546  1.00 52.06           N  
ATOM   1614  CA  ARG A 275      32.111  97.446   7.373  1.00 52.84           C  
ATOM   1615  C   ARG A 275      32.245  98.872   7.911  1.00 53.63           C  
ATOM   1616  O   ARG A 275      33.332  99.284   8.337  1.00 51.16           O  
ATOM   1617  CB  ARG A 275      31.969  96.476   8.555  1.00 52.46           C  
ATOM   1618  CG  ARG A 275      31.611  95.040   8.185  1.00 52.44           C  
ATOM   1619  CD  ARG A 275      30.115  94.838   7.967  1.00 53.03           C  
ATOM   1620  NE  ARG A 275      29.318  95.079   9.176  1.00 51.31           N  
ATOM   1621  CZ  ARG A 275      29.061  94.194  10.146  1.00 48.69           C  
ATOM   1622  NH1 ARG A 275      29.528  92.944  10.112  1.00 47.58           N  
ATOM   1623  NH2 ARG A 275      28.318  94.578  11.180  1.00 47.94           N  
ATOM   1624  N   LYS A 276      31.132  99.607   7.897  1.00 55.26           N  
ATOM   1625  CA  LYS A 276      31.058 100.940   8.505  1.00 57.59           C  
ATOM   1626  C   LYS A 276      31.077 100.814  10.033  1.00 56.72           C  
ATOM   1627  O   LYS A 276      31.644 101.666  10.722  1.00 58.77           O  
ATOM   1628  CB  LYS A 276      29.784 101.673   8.072  1.00 60.17           C  
ATOM   1629  CG  LYS A 276      29.581 101.785   6.564  1.00 62.33           C  
ATOM   1630  CD  LYS A 276      28.142 101.475   6.164  1.00 65.06           C  
ATOM   1631  CE  LYS A 276      28.026 101.101   4.689  1.00 67.49           C  
ATOM   1632  NZ  LYS A 276      26.615 101.104   4.198  1.00 68.16           N  
ATOM   1633  N   THR A 277      30.442  99.750  10.536  1.00 54.19           N  
ATOM   1634  CA  THR A 277      30.428  99.375  11.958  1.00 53.50           C  
ATOM   1635  C   THR A 277      31.748  99.620  12.704  1.00 51.25           C  
ATOM   1636  O   THR A 277      32.834  99.353  12.186  1.00 49.86           O  
ATOM   1637  CB  THR A 277      30.088  97.869  12.118  1.00 54.75           C  
ATOM   1638  OG1 THR A 277      28.955  97.528  11.312  1.00 56.97           O  
ATOM   1639  CG2 THR A 277      29.786  97.510  13.562  1.00 54.18           C  
ATOM   1640  N   SER A 278      31.628 100.124  13.927  1.00 50.54           N  
ATOM   1641  CA  SER A 278      32.753 100.238  14.861  1.00 50.34           C  
ATOM   1642  C   SER A 278      33.484  98.902  15.077  1.00 50.38           C  
ATOM   1643  O   SER A 278      32.872  97.835  15.027  1.00 50.07           O  
ATOM   1644  CB  SER A 278      32.240 100.750  16.211  1.00 50.78           C  
ATOM   1645  OG  SER A 278      33.209 100.583  17.225  1.00 51.58           O  
ATOM   1646  N   ARG A 279      34.784  98.977  15.349  1.00 49.11           N  
ATOM   1647  CA  ARG A 279      35.602  97.786  15.592  1.00 49.03           C  
ATOM   1648  C   ARG A 279      35.238  97.056  16.900  1.00 49.82           C  
ATOM   1649  O   ARG A 279      35.399  95.834  16.979  1.00 49.43           O  
ATOM   1650  CB  ARG A 279      37.083  98.164  15.575  1.00 50.66           C  
ATOM   1651  CG  ARG A 279      38.059  97.000  15.577  1.00 52.10           C  
ATOM   1652  CD  ARG A 279      39.482  97.504  15.388  1.00 53.80           C  
ATOM   1653  NE  ARG A 279      40.456  96.693  16.129  1.00 57.43           N  
ATOM   1654  CZ  ARG A 279      41.313  95.808  15.610  1.00 59.31           C  
ATOM   1655  NH1 ARG A 279      41.376  95.566  14.302  1.00 60.13           N  
ATOM   1656  NH2 ARG A 279      42.136  95.151  16.424  1.00 61.00           N  
ATOM   1657  N   VAL A 280      34.743  97.788  17.907  1.00 49.90           N  
ATOM   1658  CA  VAL A 280      34.277  97.165  19.164  1.00 50.20           C  
ATOM   1659  C   VAL A 280      32.938  96.444  18.986  1.00 50.94           C  
ATOM   1660  O   VAL A 280      32.705  95.413  19.620  1.00 50.95           O  
ATOM   1661  CB  VAL A 280      34.196  98.153  20.371  1.00 51.37           C  
ATOM   1662  CG1 VAL A 280      35.539  98.834  20.604  1.00 51.35           C  
ATOM   1663  CG2 VAL A 280      33.072  99.184  20.224  1.00 51.12           C  
ATOM   1664  N   MET A 281      32.059  96.998  18.147  1.00 52.31           N  
ATOM   1665  CA  MET A 281      30.817  96.315  17.748  1.00 52.25           C  
ATOM   1666  C   MET A 281      31.107  95.013  17.004  1.00 48.14           C  
ATOM   1667  O   MET A 281      30.420  94.015  17.219  1.00 46.15           O  
ATOM   1668  CB  MET A 281      29.952  97.210  16.852  1.00 56.64           C  
ATOM   1669  CG  MET A 281      29.282  98.396  17.527  1.00 62.41           C  
ATOM   1670  SD  MET A 281      28.255  97.984  18.953  1.00 72.33           S  
ATOM   1671  CE  MET A 281      29.346  98.455  20.294  1.00 70.94           C  
ATOM   1672  N   LEU A 282      32.116  95.033  16.131  1.00 45.30           N  
ATOM   1673  CA  LEU A 282      32.525  93.838  15.386  1.00 43.95           C  
ATOM   1674  C   LEU A 282      33.117  92.759  16.288  1.00 44.11           C  
ATOM   1675  O   LEU A 282      32.955  91.578  16.006  1.00 43.66           O  
ATOM   1676  CB  LEU A 282      33.526  94.185  14.278  1.00 42.04           C  
ATOM   1677  CG  LEU A 282      33.045  95.081  13.138  1.00 40.75           C  
ATOM   1678  CD1 LEU A 282      34.210  95.411  12.218  1.00 40.02           C  
ATOM   1679  CD2 LEU A 282      31.907  94.436  12.363  1.00 40.94           C  
ATOM   1680  N   MET A 283      33.812  93.162  17.350  1.00 46.89           N  
ATOM   1681  CA  MET A 283      34.345  92.208  18.330  1.00 49.64           C  
ATOM   1682  C   MET A 283      33.224  91.528  19.120  1.00 47.52           C  
ATOM   1683  O   MET A 283      33.314  90.336  19.409  1.00 44.65           O  
ATOM   1684  CB  MET A 283      35.359  92.880  19.265  1.00 55.16           C  
ATOM   1685  CG  MET A 283      36.698  93.162  18.592  1.00 59.76           C  
ATOM   1686  SD  MET A 283      37.741  94.343  19.478  1.00 68.21           S  
ATOM   1687  CE  MET A 283      39.259  94.244  18.525  1.00 65.97           C  
ATOM   1688  N   ARG A 284      32.161  92.270  19.433  1.00 47.22           N  
ATOM   1689  CA  ARG A 284      30.956  91.688  20.044  1.00 47.83           C  
ATOM   1690  C   ARG A 284      30.241  90.706  19.097  1.00 46.26           C  
ATOM   1691  O   ARG A 284      29.766  89.658  19.536  1.00 45.91           O  
ATOM   1692  CB  ARG A 284      29.996  92.786  20.504  1.00 51.73           C  
ATOM   1693  CG  ARG A 284      30.558  93.626  21.642  1.00 56.93           C  
ATOM   1694  CD  ARG A 284      29.664  94.807  22.004  1.00 62.14           C  
ATOM   1695  NE  ARG A 284      30.410  95.889  22.664  1.00 66.80           N  
ATOM   1696  CZ  ARG A 284      29.866  96.966  23.238  1.00 68.96           C  
ATOM   1697  NH1 ARG A 284      28.545  97.146  23.261  1.00 71.12           N  
ATOM   1698  NH2 ARG A 284      30.655  97.880  23.798  1.00 70.42           N  
ATOM   1699  N   GLU A 285      30.174  91.041  17.808  1.00 43.88           N  
ATOM   1700  CA  GLU A 285      29.692  90.105  16.790  1.00 43.38           C  
ATOM   1701  C   GLU A 285      30.536  88.823  16.766  1.00 42.48           C  
ATOM   1702  O   GLU A 285      29.994  87.716  16.682  1.00 42.29           O  
ATOM   1703  CB  GLU A 285      29.680  90.750  15.392  1.00 44.38           C  
ATOM   1704  CG  GLU A 285      28.563  91.763  15.158  1.00 45.77           C  
ATOM   1705  CD  GLU A 285      28.389  92.177  13.693  1.00 46.95           C  
ATOM   1706  OE1 GLU A 285      29.085  91.654  12.796  1.00 48.21           O  
ATOM   1707  OE2 GLU A 285      27.533  93.044  13.420  1.00 47.54           O  
ATOM   1708  N   HIS A 286      31.856  88.982  16.856  1.00 40.33           N  
ATOM   1709  CA  HIS A 286      32.787  87.851  16.779  1.00 39.56           C  
ATOM   1710  C   HIS A 286      32.868  86.962  18.021  1.00 36.50           C  
ATOM   1711  O   HIS A 286      33.299  85.814  17.909  1.00 35.89           O  
ATOM   1712  CB  HIS A 286      34.188  88.332  16.387  1.00 41.76           C  
ATOM   1713  CG  HIS A 286      34.251  88.931  15.016  1.00 44.13           C  
ATOM   1714  ND1 HIS A 286      35.309  89.703  14.585  1.00 45.37           N  
ATOM   1715  CD2 HIS A 286      33.370  88.894  13.990  1.00 45.14           C  
ATOM   1716  CE1 HIS A 286      35.086  90.098  13.346  1.00 45.90           C  
ATOM   1717  NE2 HIS A 286      33.915  89.623  12.961  1.00 46.70           N  
ATOM   1718  N   LYS A 287      32.484  87.479  19.190  1.00 35.63           N  
ATOM   1719  CA  LYS A 287      32.360  86.646  20.402  1.00 34.63           C  
ATOM   1720  C   LYS A 287      31.226  85.640  20.230  1.00 32.15           C  
ATOM   1721  O   LYS A 287      31.372  84.468  20.589  1.00 32.22           O  
ATOM   1722  CB  LYS A 287      32.111  87.486  21.668  1.00 35.71           C  
ATOM   1723  CG  LYS A 287      33.270  88.359  22.145  1.00 37.38           C  
ATOM   1724  CD  LYS A 287      34.598  87.618  22.212  1.00 39.95           C  
ATOM   1725  CE  LYS A 287      35.599  88.322  23.121  1.00 41.97           C  
ATOM   1726  NZ  LYS A 287      36.956  87.708  23.028  1.00 43.33           N  
ATOM   1727  N   ALA A 288      30.107  86.106  19.677  1.00 29.27           N  
ATOM   1728  CA  ALA A 288      28.973  85.236  19.356  1.00 27.94           C  
ATOM   1729  C   ALA A 288      29.330  84.198  18.294  1.00 27.06           C  
ATOM   1730  O   ALA A 288      28.946  83.033  18.425  1.00 26.22           O  
ATOM   1731  CB  ALA A 288      27.781  86.061  18.903  1.00 28.18           C  
ATOM   1732  N   LEU A 289      30.060  84.617  17.254  1.00 26.44           N  
ATOM   1733  CA  LEU A 289      30.543  83.682  16.219  1.00 26.61           C  
ATOM   1734  C   LEU A 289      31.474  82.610  16.784  1.00 25.97           C  
ATOM   1735  O   LEU A 289      31.424  81.454  16.363  1.00 24.49           O  
ATOM   1736  CB  LEU A 289      31.252  84.422  15.072  1.00 26.73           C  
ATOM   1737  CG  LEU A 289      30.376  85.184  14.065  1.00 26.65           C  
ATOM   1738  CD1 LEU A 289      31.253  85.815  12.998  1.00 26.58           C  
ATOM   1739  CD2 LEU A 289      29.326  84.288  13.424  1.00 26.49           C  
ATOM   1740  N   LYS A 290      32.314  83.011  17.738  1.00 26.05           N  
ATOM   1741  CA  LYS A 290      33.194  82.090  18.444  1.00 25.70           C  
ATOM   1742  C   LYS A 290      32.445  80.994  19.212  1.00 23.86           C  
ATOM   1743  O   LYS A 290      32.866  79.839  19.184  1.00 22.70           O  
ATOM   1744  CB  LYS A 290      34.113  82.861  19.391  1.00 27.66           C  
ATOM   1745  CG  LYS A 290      35.047  81.969  20.184  1.00 29.89           C  
ATOM   1746  CD  LYS A 290      36.244  82.727  20.720  1.00 32.38           C  
ATOM   1747  CE  LYS A 290      37.204  81.762  21.392  1.00 34.17           C  
ATOM   1748  NZ  LYS A 290      38.214  82.459  22.220  1.00 35.91           N  
ATOM   1749  N   THR A 291      31.365  81.353  19.908  1.00 22.49           N  
ATOM   1750  CA  THR A 291      30.514  80.356  20.569  1.00 22.55           C  
ATOM   1751  C   THR A 291      30.085  79.244  19.584  1.00 22.06           C  
ATOM   1752  O   THR A 291      30.163  78.049  19.900  1.00 21.62           O  
ATOM   1753  CB  THR A 291      29.253  81.003  21.204  1.00 22.97           C  
ATOM   1754  OG1 THR A 291      29.640  82.039  22.119  1.00 22.71           O  
ATOM   1755  CG2 THR A 291      28.405  79.964  21.952  1.00 22.68           C  
ATOM   1756  N   LEU A 292      29.663  79.652  18.389  1.00 21.17           N  
ATOM   1757  CA  LEU A 292      29.164  78.718  17.380  1.00 21.09           C  
ATOM   1758  C   LEU A 292      30.250  77.784  16.868  1.00 20.65           C  
ATOM   1759  O   LEU A 292      30.037  76.574  16.767  1.00 21.15           O  
ATOM   1760  CB  LEU A 292      28.533  79.470  16.207  1.00 21.08           C  
ATOM   1761  CG  LEU A 292      27.342  80.360  16.550  1.00 21.09           C  
ATOM   1762  CD1 LEU A 292      26.970  81.208  15.344  1.00 21.31           C  
ATOM   1763  CD2 LEU A 292      26.159  79.527  17.039  1.00 21.28           C  
ATOM   1764  N   GLY A 293      31.411  78.343  16.556  1.00 20.30           N  
ATOM   1765  CA  GLY A 293      32.571  77.544  16.169  1.00 20.06           C  
ATOM   1766  C   GLY A 293      33.033  76.545  17.220  1.00 20.14           C  
ATOM   1767  O   GLY A 293      33.504  75.456  16.865  1.00 20.45           O  
ATOM   1768  N   ILE A 294      32.912  76.907  18.504  1.00 19.37           N  
ATOM   1769  CA  ILE A 294      33.222  75.989  19.605  1.00 18.82           C  
ATOM   1770  C   ILE A 294      32.243  74.816  19.588  1.00 18.51           C  
ATOM   1771  O   ILE A 294      32.652  73.659  19.608  1.00 17.85           O  
ATOM   1772  CB  ILE A 294      33.211  76.696  20.991  1.00 18.94           C  
ATOM   1773  CG1 ILE A 294      34.383  77.670  21.104  1.00 19.20           C  
ATOM   1774  CG2 ILE A 294      33.323  75.687  22.127  1.00 18.81           C  
ATOM   1775  CD1 ILE A 294      34.211  78.718  22.189  1.00 19.44           C  
ATOM   1776  N   ILE A 295      30.950  75.126  19.542  1.00 19.30           N  
ATOM   1777  CA  ILE A 295      29.899  74.099  19.403  1.00 19.11           C  
ATOM   1778  C   ILE A 295      30.202  73.210  18.194  1.00 18.99           C  
ATOM   1779  O   ILE A 295      30.114  71.983  18.274  1.00 18.34           O  
ATOM   1780  CB  ILE A 295      28.489  74.737  19.296  1.00 19.24           C  
ATOM   1781  CG1 ILE A 295      28.064  75.309  20.658  1.00 19.58           C  
ATOM   1782  CG2 ILE A 295      27.449  73.733  18.800  1.00 19.23           C  
ATOM   1783  CD1 ILE A 295      26.960  76.353  20.574  1.00 20.06           C  
ATOM   1784  N   MET A 296      30.592  73.834  17.085  1.00 19.52           N  
ATOM   1785  CA  MET A 296      30.924  73.082  15.873  1.00 20.12           C  
ATOM   1786  C   MET A 296      32.124  72.173  16.074  1.00 20.19           C  
ATOM   1787  O   MET A 296      32.069  70.997  15.740  1.00 21.24           O  
ATOM   1788  CB  MET A 296      31.149  74.028  14.694  1.00 20.35           C  
ATOM   1789  CG  MET A 296      29.855  74.610  14.157  1.00 20.44           C  
ATOM   1790  SD  MET A 296      30.117  75.906  12.938  1.00 21.40           S  
ATOM   1791  CE  MET A 296      28.458  76.566  12.818  1.00 21.46           C  
ATOM   1792  N   GLY A 297      33.192  72.718  16.643  1.00 20.54           N  
ATOM   1793  CA  GLY A 297      34.405  71.955  16.913  1.00 20.41           C  
ATOM   1794  C   GLY A 297      34.195  70.780  17.842  1.00 20.56           C  
ATOM   1795  O   GLY A 297      34.690  69.680  17.578  1.00 20.46           O  
ATOM   1796  N   VAL A 298      33.462  71.011  18.931  1.00 20.62           N  
ATOM   1797  CA  VAL A 298      33.201  69.967  19.923  1.00 20.88           C  
ATOM   1798  C   VAL A 298      32.308  68.863  19.351  1.00 20.72           C  
ATOM   1799  O   VAL A 298      32.520  67.692  19.654  1.00 20.71           O  
ATOM   1800  CB  VAL A 298      32.618  70.556  21.235  1.00 21.56           C  
ATOM   1801  CG1 VAL A 298      32.152  69.461  22.193  1.00 22.58           C  
ATOM   1802  CG2 VAL A 298      33.666  71.400  21.932  1.00 20.89           C  
ATOM   1803  N   PHE A 299      31.325  69.232  18.526  1.00 20.88           N  
ATOM   1804  CA  PHE A 299      30.453  68.254  17.862  1.00 20.18           C  
ATOM   1805  C   PHE A 299      31.262  67.287  17.019  1.00 20.46           C  
ATOM   1806  O   PHE A 299      31.000  66.075  17.034  1.00 20.96           O  
ATOM   1807  CB  PHE A 299      29.410  68.963  16.992  1.00 20.44           C  
ATOM   1808  CG  PHE A 299      28.389  68.043  16.387  1.00 19.96           C  
ATOM   1809  CD1 PHE A 299      27.228  67.716  17.083  1.00 20.43           C  
ATOM   1810  CD2 PHE A 299      28.585  67.498  15.128  1.00 19.95           C  
ATOM   1811  CE1 PHE A 299      26.271  66.866  16.528  1.00 20.65           C  
ATOM   1812  CE2 PHE A 299      27.644  66.641  14.568  1.00 20.39           C  
ATOM   1813  CZ  PHE A 299      26.480  66.326  15.267  1.00 20.78           C  
ATOM   1814  N   THR A 300      32.244  67.830  16.297  1.00 20.63           N  
ATOM   1815  CA  THR A 300      33.169  67.045  15.471  1.00 21.55           C  
ATOM   1816  C   THR A 300      34.007  66.069  16.304  1.00 22.83           C  
ATOM   1817  O   THR A 300      34.091  64.880  15.983  1.00 22.96           O  
ATOM   1818  CB  THR A 300      34.113  67.973  14.674  1.00 21.49           C  
ATOM   1819  OG1 THR A 300      33.335  68.890  13.890  1.00 21.53           O  
ATOM   1820  CG2 THR A 300      35.018  67.179  13.751  1.00 21.63           C  
ATOM   1821  N   LEU A 301      34.626  66.576  17.370  1.00 24.11           N  
ATOM   1822  CA  LEU A 301      35.375  65.732  18.296  1.00 24.60           C  
ATOM   1823  C   LEU A 301      34.516  64.614  18.898  1.00 23.68           C  
ATOM   1824  O   LEU A 301      34.989  63.486  19.068  1.00 23.17           O  
ATOM   1825  CB  LEU A 301      35.989  66.569  19.428  1.00 26.25           C  
ATOM   1826  CG  LEU A 301      37.173  67.477  19.081  1.00 28.45           C  
ATOM   1827  CD1 LEU A 301      37.733  68.086  20.356  1.00 29.30           C  
ATOM   1828  CD2 LEU A 301      38.274  66.732  18.337  1.00 29.34           C  
ATOM   1829  N   CYS A 302      33.261  64.927  19.210  1.00 22.49           N  
ATOM   1830  CA  CYS A 302      32.379  63.973  19.867  1.00 22.06           C  
ATOM   1831  C   CYS A 302      31.881  62.875  18.930  1.00 21.25           C  
ATOM   1832  O   CYS A 302      31.796  61.719  19.346  1.00 21.19           O  
ATOM   1833  CB  CYS A 302      31.204  64.692  20.544  1.00 22.97           C  
ATOM   1834  SG  CYS A 302      31.663  65.610  22.042  1.00 24.80           S  
ATOM   1835  N   TRP A 303      31.575  63.219  17.675  1.00 20.42           N  
ATOM   1836  CA  TRP A 303      30.923  62.280  16.750  1.00 19.78           C  
ATOM   1837  C   TRP A 303      31.814  61.641  15.681  1.00 20.06           C  
ATOM   1838  O   TRP A 303      31.552  60.504  15.282  1.00 19.26           O  
ATOM   1839  CB  TRP A 303      29.703  62.947  16.089  1.00 19.53           C  
ATOM   1840  CG  TRP A 303      28.487  62.966  16.994  1.00 18.57           C  
ATOM   1841  CD1 TRP A 303      27.887  64.060  17.535  1.00 18.14           C  
ATOM   1842  CD2 TRP A 303      27.746  61.829  17.461  1.00 17.91           C  
ATOM   1843  NE1 TRP A 303      26.815  63.680  18.305  1.00 17.92           N  
ATOM   1844  CE2 TRP A 303      26.706  62.316  18.278  1.00 17.64           C  
ATOM   1845  CE3 TRP A 303      27.859  60.443  17.260  1.00 17.62           C  
ATOM   1846  CZ2 TRP A 303      25.779  61.473  18.895  1.00 17.66           C  
ATOM   1847  CZ3 TRP A 303      26.939  59.600  17.881  1.00 17.59           C  
ATOM   1848  CH2 TRP A 303      25.916  60.119  18.695  1.00 17.59           C  
ATOM   1849  N   LEU A 304      32.848  62.349  15.213  1.00 20.95           N  
ATOM   1850  CA  LEU A 304      33.696  61.828  14.120  1.00 21.53           C  
ATOM   1851  C   LEU A 304      34.392  60.501  14.456  1.00 21.66           C  
ATOM   1852  O   LEU A 304      34.526  59.656  13.579  1.00 22.29           O  
ATOM   1853  CB  LEU A 304      34.725  62.862  13.634  1.00 21.90           C  
ATOM   1854  CG  LEU A 304      35.658  62.437  12.484  1.00 22.62           C  
ATOM   1855  CD1 LEU A 304      34.857  61.992  11.263  1.00 23.02           C  
ATOM   1856  CD2 LEU A 304      36.627  63.555  12.099  1.00 22.82           C  
ATOM   1857  N   PRO A 305      34.836  60.311  15.714  1.00 21.45           N  
ATOM   1858  CA  PRO A 305      35.373  58.991  16.059  1.00 21.38           C  
ATOM   1859  C   PRO A 305      34.376  57.848  15.873  1.00 21.14           C  
ATOM   1860  O   PRO A 305      34.731  56.842  15.272  1.00 20.60           O  
ATOM   1861  CB  PRO A 305      35.770  59.141  17.532  1.00 21.73           C  
ATOM   1862  CG  PRO A 305      36.077  60.590  17.672  1.00 21.93           C  
ATOM   1863  CD  PRO A 305      35.116  61.305  16.764  1.00 21.55           C  
ATOM   1864  N   PHE A 306      33.149  58.012  16.372  1.00 21.65           N  
ATOM   1865  CA  PHE A 306      32.105  56.986  16.222  1.00 21.67           C  
ATOM   1866  C   PHE A 306      31.851  56.639  14.755  1.00 21.33           C  
ATOM   1867  O   PHE A 306      31.797  55.464  14.398  1.00 20.30           O  
ATOM   1868  CB  PHE A 306      30.778  57.415  16.882  1.00 21.77           C  
ATOM   1869  CG  PHE A 306      29.634  56.484  16.577  1.00 21.55           C  
ATOM   1870  CD1 PHE A 306      29.489  55.291  17.272  1.00 21.68           C  
ATOM   1871  CD2 PHE A 306      28.728  56.780  15.562  1.00 21.60           C  
ATOM   1872  CE1 PHE A 306      28.451  54.413  16.977  1.00 21.92           C  
ATOM   1873  CE2 PHE A 306      27.691  55.910  15.258  1.00 21.93           C  
ATOM   1874  CZ  PHE A 306      27.551  54.721  15.966  1.00 22.11           C  
ATOM   1875  N   PHE A 307      31.695  57.664  13.922  1.00 21.93           N  
ATOM   1876  CA  PHE A 307      31.386  57.463  12.501  1.00 23.22           C  
ATOM   1877  C   PHE A 307      32.546  56.837  11.704  1.00 24.85           C  
ATOM   1878  O   PHE A 307      32.298  56.068  10.784  1.00 24.51           O  
ATOM   1879  CB  PHE A 307      30.860  58.754  11.846  1.00 22.79           C  
ATOM   1880  CG  PHE A 307      29.402  59.008  12.123  1.00 22.98           C  
ATOM   1881  CD1 PHE A 307      28.413  58.332  11.406  1.00 23.79           C  
ATOM   1882  CD2 PHE A 307      29.005  59.885  13.122  1.00 23.05           C  
ATOM   1883  CE1 PHE A 307      27.064  58.545  11.669  1.00 23.57           C  
ATOM   1884  CE2 PHE A 307      27.657  60.107  13.386  1.00 23.35           C  
ATOM   1885  CZ  PHE A 307      26.686  59.435  12.662  1.00 23.33           C  
ATOM   1886  N   LEU A 308      33.795  57.147  12.055  1.00 26.59           N  
ATOM   1887  CA  LEU A 308      34.946  56.472  11.436  1.00 28.40           C  
ATOM   1888  C   LEU A 308      34.993  54.996  11.859  1.00 29.89           C  
ATOM   1889  O   LEU A 308      35.191  54.101  11.036  1.00 29.23           O  
ATOM   1890  CB  LEU A 308      36.263  57.169  11.805  1.00 28.31           C  
ATOM   1891  CG  LEU A 308      36.460  58.587  11.244  1.00 28.64           C  
ATOM   1892  CD1 LEU A 308      37.640  59.264  11.923  1.00 28.25           C  
ATOM   1893  CD2 LEU A 308      36.636  58.590   9.731  1.00 28.56           C  
ATOM   1894  N   VAL A 309      34.803  54.765  13.151  1.00 31.29           N  
ATOM   1895  CA  VAL A 309      34.784  53.417  13.720  1.00 33.39           C  
ATOM   1896  C   VAL A 309      33.597  52.584  13.221  1.00 34.53           C  
ATOM   1897  O   VAL A 309      33.731  51.378  13.029  1.00 36.06           O  
ATOM   1898  CB  VAL A 309      34.856  53.490  15.273  1.00 34.10           C  
ATOM   1899  CG1 VAL A 309      34.047  52.403  15.967  1.00 34.88           C  
ATOM   1900  CG2 VAL A 309      36.311  53.457  15.711  1.00 34.36           C  
ATOM   1901  N   ASN A 310      32.448  53.227  13.026  1.00 36.02           N  
ATOM   1902  CA  ASN A 310      31.269  52.581  12.435  1.00 36.15           C  
ATOM   1903  C   ASN A 310      31.555  51.994  11.044  1.00 36.12           C  
ATOM   1904  O   ASN A 310      31.076  50.903  10.733  1.00 36.73           O  
ATOM   1905  CB  ASN A 310      30.109  53.588  12.378  1.00 36.27           C  
ATOM   1906  CG  ASN A 310      28.822  52.996  11.826  1.00 36.32           C  
ATOM   1907  OD1 ASN A 310      28.224  53.548  10.908  1.00 38.15           O  
ATOM   1908  ND2 ASN A 310      28.380  51.888  12.394  1.00 35.77           N  
ATOM   1909  N   ILE A 311      32.348  52.700  10.232  1.00 35.64           N  
ATOM   1910  CA  ILE A 311      32.746  52.213   8.898  1.00 35.85           C  
ATOM   1911  C   ILE A 311      33.722  51.036   9.007  1.00 36.22           C  
ATOM   1912  O   ILE A 311      33.533  50.002   8.365  1.00 35.69           O  
ATOM   1913  CB  ILE A 311      33.378  53.331   8.030  1.00 35.62           C  
ATOM   1914  CG1 ILE A 311      32.382  54.482   7.789  1.00 35.20           C  
ATOM   1915  CG2 ILE A 311      33.862  52.778   6.692  1.00 35.98           C  
ATOM   1916  CD1 ILE A 311      31.054  54.084   7.179  1.00 35.15           C  
ATOM   1917  N   VAL A 312      34.756  51.196   9.829  1.00 36.56           N  
ATOM   1918  CA  VAL A 312      35.723  50.117  10.085  1.00 35.99           C  
ATOM   1919  C   VAL A 312      34.991  48.846  10.563  1.00 36.21           C  
ATOM   1920  O   VAL A 312      35.310  47.742  10.129  1.00 35.25           O  
ATOM   1921  CB  VAL A 312      36.812  50.559  11.109  1.00 35.29           C  
ATOM   1922  CG1 VAL A 312      37.686  49.386  11.543  1.00 34.89           C  
ATOM   1923  CG2 VAL A 312      37.684  51.667  10.528  1.00 34.60           C  
ATOM   1924  N   ASN A 313      33.997  49.016  11.433  1.00 37.70           N  
ATOM   1925  CA  ASN A 313      33.276  47.887  12.021  1.00 39.28           C  
ATOM   1926  C   ASN A 313      32.358  47.117  11.051  1.00 40.53           C  
ATOM   1927  O   ASN A 313      32.187  45.905  11.211  1.00 39.73           O  
ATOM   1928  CB  ASN A 313      32.481  48.351  13.244  1.00 40.12           C  
ATOM   1929  CG  ASN A 313      31.980  47.194  14.087  1.00 40.65           C  
ATOM   1930  OD1 ASN A 313      32.768  46.403  14.612  1.00 41.20           O  
ATOM   1931  ND2 ASN A 313      30.665  47.083  14.218  1.00 42.93           N  
ATOM   1932  N   VAL A 314      31.767  47.794  10.063  1.00 41.51           N  
ATOM   1933  CA  VAL A 314      30.990  47.077   9.030  1.00 42.72           C  
ATOM   1934  C   VAL A 314      31.861  46.269   8.063  1.00 42.68           C  
ATOM   1935  O   VAL A 314      31.386  45.287   7.502  1.00 44.38           O  
ATOM   1936  CB  VAL A 314      30.002  47.972   8.227  1.00 42.75           C  
ATOM   1937  CG1 VAL A 314      28.946  48.545   9.156  1.00 42.25           C  
ATOM   1938  CG2 VAL A 314      30.708  49.069   7.427  1.00 42.88           C  
ATOM   1939  N   PHE A 315      33.111  46.682   7.856  1.00 43.58           N  
ATOM   1940  CA  PHE A 315      34.037  45.925   6.998  1.00 44.94           C  
ATOM   1941  C   PHE A 315      34.655  44.744   7.730  1.00 45.79           C  
ATOM   1942  O   PHE A 315      34.861  43.685   7.133  1.00 47.32           O  
ATOM   1943  CB  PHE A 315      35.130  46.829   6.415  1.00 45.05           C  
ATOM   1944  CG  PHE A 315      34.623  47.755   5.355  1.00 46.32           C  
ATOM   1945  CD1 PHE A 315      34.064  47.239   4.194  1.00 48.38           C  
ATOM   1946  CD2 PHE A 315      34.673  49.134   5.514  1.00 47.51           C  
ATOM   1947  CE1 PHE A 315      33.570  48.073   3.210  1.00 48.55           C  
ATOM   1948  CE2 PHE A 315      34.180  49.978   4.528  1.00 48.19           C  
ATOM   1949  CZ  PHE A 315      33.628  49.446   3.373  1.00 48.53           C  
ATOM   1950  N   ASN A 316      34.947  44.930   9.016  1.00 44.86           N  
ATOM   1951  CA  ASN A 316      35.514  43.874   9.846  1.00 42.19           C  
ATOM   1952  C   ASN A 316      35.097  44.087  11.297  1.00 40.95           C  
ATOM   1953  O   ASN A 316      35.508  45.061  11.928  1.00 41.56           O  
ATOM   1954  CB  ASN A 316      37.039  43.889   9.706  1.00 42.00           C  
ATOM   1955  CG  ASN A 316      37.694  42.619  10.212  1.00 41.96           C  
ATOM   1956  OD1 ASN A 316      37.081  41.805  10.905  1.00 41.28           O  
ATOM   1957  ND2 ASN A 316      38.962  42.448   9.868  1.00 42.22           N  
ATOM   1958  N   ARG A 317      34.279  43.180  11.821  1.00 39.45           N  
ATOM   1959  CA  ARG A 317      33.747  43.324  13.178  1.00 40.23           C  
ATOM   1960  C   ARG A 317      34.812  43.118  14.270  1.00 38.73           C  
ATOM   1961  O   ARG A 317      34.683  43.670  15.364  1.00 38.70           O  
ATOM   1962  CB  ARG A 317      32.511  42.432  13.379  1.00 42.46           C  
ATOM   1963  CG  ARG A 317      31.364  42.852  12.459  1.00 45.04           C  
ATOM   1964  CD  ARG A 317      30.087  42.031  12.592  1.00 47.30           C  
ATOM   1965  NE  ARG A 317      29.111  42.408  11.553  1.00 49.60           N  
ATOM   1966  CZ  ARG A 317      28.032  41.701  11.196  1.00 50.53           C  
ATOM   1967  NH1 ARG A 317      27.730  40.540  11.780  1.00 51.86           N  
ATOM   1968  NH2 ARG A 317      27.237  42.165  10.236  1.00 52.12           N  
ATOM   1969  N   ASP A 318      35.873  42.375  13.952  1.00 38.05           N  
ATOM   1970  CA  ASP A 318      36.992  42.147  14.879  1.00 37.75           C  
ATOM   1971  C   ASP A 318      37.903  43.361  15.080  1.00 36.98           C  
ATOM   1972  O   ASP A 318      38.631  43.411  16.063  1.00 36.71           O  
ATOM   1973  CB  ASP A 318      37.866  40.983  14.407  1.00 38.67           C  
ATOM   1974  CG  ASP A 318      37.104  39.681  14.294  1.00 40.34           C  
ATOM   1975  OD1 ASP A 318      36.266  39.393  15.175  1.00 42.13           O  
ATOM   1976  OD2 ASP A 318      37.347  38.940  13.319  1.00 41.26           O  
ATOM   1977  N   LEU A 319      37.888  44.314  14.150  1.00 37.30           N  
ATOM   1978  CA  LEU A 319      38.698  45.532  14.280  1.00 37.57           C  
ATOM   1979  C   LEU A 319      38.192  46.497  15.352  1.00 36.89           C  
ATOM   1980  O   LEU A 319      38.957  47.332  15.820  1.00 36.79           O  
ATOM   1981  CB  LEU A 319      38.812  46.270  12.935  1.00 38.42           C  
ATOM   1982  CG  LEU A 319      39.776  45.682  11.895  1.00 39.00           C  
ATOM   1983  CD1 LEU A 319      39.717  46.492  10.609  1.00 38.88           C  
ATOM   1984  CD2 LEU A 319      41.204  45.639  12.425  1.00 39.10           C  
ATOM   1985  N   VAL A 320      36.918  46.391  15.728  1.00 37.03           N  
ATOM   1986  CA  VAL A 320      36.325  47.236  16.761  1.00 37.62           C  
ATOM   1987  C   VAL A 320      35.506  46.359  17.718  1.00 37.26           C  
ATOM   1988  O   VAL A 320      34.397  45.929  17.364  1.00 40.68           O  
ATOM   1989  CB  VAL A 320      35.427  48.330  16.135  1.00 38.59           C  
ATOM   1990  CG1 VAL A 320      34.785  49.209  17.207  1.00 39.45           C  
ATOM   1991  CG2 VAL A 320      36.229  49.187  15.171  1.00 39.07           C  
ATOM   1992  N   PRO A 321      36.034  46.099  18.934  1.00 35.68           N  
ATOM   1993  CA  PRO A 321      35.232  45.391  19.933  1.00 35.71           C  
ATOM   1994  C   PRO A 321      33.956  46.154  20.270  1.00 36.26           C  
ATOM   1995  O   PRO A 321      33.952  47.388  20.256  1.00 37.78           O  
ATOM   1996  CB  PRO A 321      36.151  45.317  21.160  1.00 35.60           C  
ATOM   1997  CG  PRO A 321      37.524  45.554  20.649  1.00 35.94           C  
ATOM   1998  CD  PRO A 321      37.391  46.406  19.427  1.00 35.85           C  
ATOM   1999  N   ASP A 322      32.897  45.416  20.581  1.00 35.86           N  
ATOM   2000  CA  ASP A 322      31.582  46.005  20.805  1.00 36.00           C  
ATOM   2001  C   ASP A 322      31.593  47.015  21.940  1.00 34.92           C  
ATOM   2002  O   ASP A 322      30.991  48.065  21.805  1.00 35.44           O  
ATOM   2003  CB  ASP A 322      30.529  44.925  21.084  1.00 37.97           C  
ATOM   2004  CG  ASP A 322      30.363  43.943  19.924  1.00 40.69           C  
ATOM   2005  OD1 ASP A 322      30.516  44.343  18.743  1.00 40.27           O  
ATOM   2006  OD2 ASP A 322      30.078  42.758  20.206  1.00 45.16           O  
ATOM   2007  N   TRP A 323      32.278  46.709  23.043  1.00 34.12           N  
ATOM   2008  CA  TRP A 323      32.341  47.634  24.189  1.00 33.69           C  
ATOM   2009  C   TRP A 323      33.027  48.965  23.819  1.00 33.14           C  
ATOM   2010  O   TRP A 323      32.645  50.028  24.319  1.00 32.61           O  
ATOM   2011  CB  TRP A 323      33.009  46.976  25.413  1.00 34.09           C  
ATOM   2012  CG  TRP A 323      34.498  46.781  25.309  1.00 34.65           C  
ATOM   2013  CD1 TRP A 323      35.156  45.648  24.911  1.00 35.40           C  
ATOM   2014  CD2 TRP A 323      35.513  47.747  25.615  1.00 34.76           C  
ATOM   2015  NE1 TRP A 323      36.519  45.852  24.947  1.00 35.35           N  
ATOM   2016  CE2 TRP A 323      36.765  47.131  25.373  1.00 34.95           C  
ATOM   2017  CE3 TRP A 323      35.486  49.076  26.064  1.00 34.17           C  
ATOM   2018  CZ2 TRP A 323      37.975  47.798  25.569  1.00 34.48           C  
ATOM   2019  CZ3 TRP A 323      36.695  49.740  26.259  1.00 34.04           C  
ATOM   2020  CH2 TRP A 323      37.920  49.099  26.008  1.00 34.39           C  
ATOM   2021  N   LEU A 324      34.018  48.890  22.933  1.00 31.53           N  
ATOM   2022  CA  LEU A 324      34.719  50.065  22.430  1.00 31.08           C  
ATOM   2023  C   LEU A 324      33.833  50.886  21.495  1.00 30.25           C  
ATOM   2024  O   LEU A 324      33.814  52.124  21.571  1.00 29.53           O  
ATOM   2025  CB  LEU A 324      35.998  49.641  21.701  1.00 31.52           C  
ATOM   2026  CG  LEU A 324      36.980  50.749  21.339  1.00 31.84           C  
ATOM   2027  CD1 LEU A 324      37.557  51.432  22.572  1.00 31.69           C  
ATOM   2028  CD2 LEU A 324      38.093  50.175  20.480  1.00 32.99           C  
ATOM   2029  N   PHE A 325      33.126  50.187  20.607  1.00 28.70           N  
ATOM   2030  CA  PHE A 325      32.050  50.775  19.796  1.00 28.15           C  
ATOM   2031  C   PHE A 325      31.064  51.565  20.670  1.00 26.50           C  
ATOM   2032  O   PHE A 325      30.732  52.717  20.359  1.00 25.57           O  
ATOM   2033  CB  PHE A 325      31.322  49.662  19.023  1.00 29.20           C  
ATOM   2034  CG  PHE A 325      30.214  50.143  18.125  1.00 30.04           C  
ATOM   2035  CD1 PHE A 325      30.483  50.508  16.813  1.00 30.35           C  
ATOM   2036  CD2 PHE A 325      28.890  50.198  18.580  1.00 30.17           C  
ATOM   2037  CE1 PHE A 325      29.464  50.935  15.973  1.00 30.85           C  
ATOM   2038  CE2 PHE A 325      27.866  50.629  17.744  1.00 30.38           C  
ATOM   2039  CZ  PHE A 325      28.152  50.994  16.434  1.00 30.49           C  
ATOM   2040  N   VAL A 326      30.630  50.951  21.769  1.00 24.93           N  
ATOM   2041  CA  VAL A 326      29.702  51.591  22.707  1.00 25.00           C  
ATOM   2042  C   VAL A 326      30.347  52.842  23.328  1.00 24.93           C  
ATOM   2043  O   VAL A 326      29.715  53.892  23.379  1.00 24.77           O  
ATOM   2044  CB  VAL A 326      29.215  50.606  23.807  1.00 25.56           C  
ATOM   2045  CG1 VAL A 326      28.327  51.302  24.826  1.00 25.84           C  
ATOM   2046  CG2 VAL A 326      28.441  49.436  23.201  1.00 25.56           C  
ATOM   2047  N   ALA A 327      31.605  52.737  23.762  1.00 24.66           N  
ATOM   2048  CA  ALA A 327      32.326  53.873  24.349  1.00 24.36           C  
ATOM   2049  C   ALA A 327      32.355  55.064  23.396  1.00 24.74           C  
ATOM   2050  O   ALA A 327      32.042  56.189  23.793  1.00 24.30           O  
ATOM   2051  CB  ALA A 327      33.743  53.473  24.742  1.00 24.35           C  
ATOM   2052  N   PHE A 328      32.724  54.811  22.139  1.00 25.63           N  
ATOM   2053  CA  PHE A 328      32.658  55.838  21.089  1.00 25.79           C  
ATOM   2054  C   PHE A 328      31.248  56.404  20.923  1.00 23.58           C  
ATOM   2055  O   PHE A 328      31.089  57.617  20.749  1.00 22.17           O  
ATOM   2056  CB  PHE A 328      33.141  55.299  19.738  1.00 28.08           C  
ATOM   2057  CG  PHE A 328      34.630  55.108  19.651  1.00 30.97           C  
ATOM   2058  CD1 PHE A 328      35.481  56.192  19.736  1.00 33.61           C  
ATOM   2059  CD2 PHE A 328      35.183  53.849  19.451  1.00 33.08           C  
ATOM   2060  CE1 PHE A 328      36.855  56.024  19.651  1.00 34.66           C  
ATOM   2061  CE2 PHE A 328      36.558  53.682  19.366  1.00 33.79           C  
ATOM   2062  CZ  PHE A 328      37.394  54.771  19.460  1.00 34.00           C  
ATOM   2063  N   ASN A 329      30.234  55.539  20.972  1.00 21.87           N  
ATOM   2064  CA  ASN A 329      28.848  56.017  20.936  1.00 21.59           C  
ATOM   2065  C   ASN A 329      28.533  56.951  22.108  1.00 22.16           C  
ATOM   2066  O   ASN A 329      27.879  57.971  21.893  1.00 22.44           O  
ATOM   2067  CB  ASN A 329      27.817  54.874  20.879  1.00 20.71           C  
ATOM   2068  CG  ASN A 329      26.515  55.256  20.151  1.00 20.25           C  
ATOM   2069  OD1 ASN A 329      25.853  54.385  19.598  1.00 19.90           O  
ATOM   2070  ND2 ASN A 329      26.133  56.532  20.158  1.00 20.22           N  
ATOM   2071  N   TRP A 330      28.999  56.624  23.316  1.00 23.16           N  
ATOM   2072  CA  TRP A 330      28.716  57.455  24.511  1.00 24.23           C  
ATOM   2073  C   TRP A 330      29.446  58.793  24.510  1.00 23.27           C  
ATOM   2074  O   TRP A 330      28.943  59.770  25.067  1.00 23.17           O  
ATOM   2075  CB  TRP A 330      28.932  56.671  25.824  1.00 25.75           C  
ATOM   2076  CG  TRP A 330      27.754  55.766  26.075  1.00 28.28           C  
ATOM   2077  CD1 TRP A 330      27.589  54.499  25.610  1.00 29.11           C  
ATOM   2078  CD2 TRP A 330      26.537  56.100  26.761  1.00 30.23           C  
ATOM   2079  NE1 TRP A 330      26.366  54.001  25.983  1.00 30.19           N  
ATOM   2080  CE2 TRP A 330      25.697  54.961  26.696  1.00 30.98           C  
ATOM   2081  CE3 TRP A 330      26.084  57.241  27.447  1.00 30.37           C  
ATOM   2082  CZ2 TRP A 330      24.428  54.926  27.288  1.00 30.85           C  
ATOM   2083  CZ3 TRP A 330      24.825  57.209  28.031  1.00 30.94           C  
ATOM   2084  CH2 TRP A 330      24.010  56.053  27.947  1.00 31.43           C  
ATOM   2085  N   LEU A 331      30.609  58.846  23.869  1.00 22.37           N  
ATOM   2086  CA  LEU A 331      31.257  60.122  23.562  1.00 21.68           C  
ATOM   2087  C   LEU A 331      30.355  60.990  22.679  1.00 21.70           C  
ATOM   2088  O   LEU A 331      30.313  62.208  22.842  1.00 22.46           O  
ATOM   2089  CB  LEU A 331      32.612  59.883  22.891  1.00 21.38           C  
ATOM   2090  CG  LEU A 331      33.439  61.082  22.447  1.00 21.20           C  
ATOM   2091  CD1 LEU A 331      33.725  62.030  23.596  1.00 21.65           C  
ATOM   2092  CD2 LEU A 331      34.736  60.588  21.833  1.00 21.35           C  
ATOM   2093  N   GLY A 332      29.633  60.365  21.750  1.00 21.78           N  
ATOM   2094  CA  GLY A 332      28.646  61.065  20.926  1.00 21.45           C  
ATOM   2095  C   GLY A 332      27.485  61.625  21.723  1.00 21.15           C  
ATOM   2096  O   GLY A 332      27.175  62.814  21.619  1.00 20.19           O  
ATOM   2097  N   TYR A 333      26.847  60.764  22.515  1.00 21.69           N  
ATOM   2098  CA  TYR A 333      25.749  61.176  23.413  1.00 22.66           C  
ATOM   2099  C   TYR A 333      26.176  62.288  24.369  1.00 23.08           C  
ATOM   2100  O   TYR A 333      25.396  63.203  24.623  1.00 24.26           O  
ATOM   2101  CB  TYR A 333      25.213  59.999  24.246  1.00 22.72           C  
ATOM   2102  CG  TYR A 333      24.545  58.855  23.487  1.00 23.04           C  
ATOM   2103  CD1 TYR A 333      23.926  59.037  22.235  1.00 23.35           C  
ATOM   2104  CD2 TYR A 333      24.503  57.582  24.051  1.00 23.54           C  
ATOM   2105  CE1 TYR A 333      23.316  57.969  21.574  1.00 23.21           C  
ATOM   2106  CE2 TYR A 333      23.896  56.518  23.402  1.00 23.66           C  
ATOM   2107  CZ  TYR A 333      23.310  56.707  22.167  1.00 23.42           C  
ATOM   2108  OH  TYR A 333      22.710  55.626  21.562  1.00 23.20           O  
ATOM   2109  N   ALA A 334      27.411  62.201  24.880  1.00 23.28           N  
ATOM   2110  CA  ALA A 334      28.023  63.239  25.736  1.00 23.36           C  
ATOM   2111  C   ALA A 334      28.013  64.659  25.152  1.00 23.37           C  
ATOM   2112  O   ALA A 334      27.975  65.632  25.899  1.00 23.10           O  
ATOM   2113  CB  ALA A 334      29.451  62.846  26.096  1.00 23.22           C  
ATOM   2114  N   ASN A 335      28.067  64.777  23.831  1.00 24.22           N  
ATOM   2115  CA  ASN A 335      27.885  66.069  23.157  1.00 25.24           C  
ATOM   2116  C   ASN A 335      26.603  66.794  23.580  1.00 25.96           C  
ATOM   2117  O   ASN A 335      26.596  68.019  23.690  1.00 25.52           O  
ATOM   2118  CB  ASN A 335      27.874  65.891  21.634  1.00 24.94           C  
ATOM   2119  CG  ASN A 335      27.740  67.204  20.903  1.00 24.82           C  
ATOM   2120  OD1 ASN A 335      26.691  67.503  20.343  1.00 26.68           O  
ATOM   2121  ND2 ASN A 335      28.781  68.010  20.942  1.00 24.41           N  
ATOM   2122  N   SER A 336      25.529  66.040  23.814  1.00 27.54           N  
ATOM   2123  CA  SER A 336      24.268  66.622  24.289  1.00 29.54           C  
ATOM   2124  C   SER A 336      24.377  67.316  25.657  1.00 30.44           C  
ATOM   2125  O   SER A 336      23.628  68.247  25.930  1.00 31.91           O  
ATOM   2126  CB  SER A 336      23.153  65.569  24.296  1.00 29.80           C  
ATOM   2127  OG  SER A 336      22.875  65.130  22.970  1.00 30.30           O  
ATOM   2128  N   ALA A 337      25.315  66.869  26.492  1.00 31.78           N  
ATOM   2129  CA  ALA A 337      25.640  67.530  27.770  1.00 32.72           C  
ATOM   2130  C   ALA A 337      26.551  68.758  27.648  1.00 33.58           C  
ATOM   2131  O   ALA A 337      26.521  69.626  28.522  1.00 33.74           O  
ATOM   2132  CB  ALA A 337      26.282  66.529  28.722  1.00 32.65           C  
ATOM   2133  N   MET A 338      27.372  68.812  26.595  1.00 34.37           N  
ATOM   2134  CA  MET A 338      28.402  69.850  26.437  1.00 34.50           C  
ATOM   2135  C   MET A 338      27.871  71.224  26.046  1.00 32.88           C  
ATOM   2136  O   MET A 338      28.379  72.236  26.528  1.00 31.27           O  
ATOM   2137  CB  MET A 338      29.441  69.430  25.388  1.00 36.49           C  
ATOM   2138  CG  MET A 338      30.250  68.190  25.746  1.00 38.57           C  
ATOM   2139  SD  MET A 338      31.328  68.392  27.177  1.00 42.64           S  
ATOM   2140  CE  MET A 338      32.545  69.535  26.522  1.00 43.76           C  
ATOM   2141  N   ASN A 339      26.879  71.267  25.160  1.00 32.87           N  
ATOM   2142  CA  ASN A 339      26.421  72.540  24.583  1.00 32.90           C  
ATOM   2143  C   ASN A 339      25.884  73.574  25.570  1.00 30.88           C  
ATOM   2144  O   ASN A 339      26.241  74.744  25.452  1.00 30.24           O  
ATOM   2145  CB  ASN A 339      25.404  72.307  23.458  1.00 34.85           C  
ATOM   2146  CG  ASN A 339      26.039  71.758  22.200  1.00 36.97           C  
ATOM   2147  OD1 ASN A 339      27.256  71.581  22.124  1.00 36.75           O  
ATOM   2148  ND2 ASN A 339      25.212  71.491  21.195  1.00 39.99           N  
ATOM   2149  N   PRO A 340      25.036  73.158  26.534  1.00 29.98           N  
ATOM   2150  CA  PRO A 340      24.595  74.101  27.567  1.00 30.23           C  
ATOM   2151  C   PRO A 340      25.746  74.650  28.395  1.00 29.88           C  
ATOM   2152  O   PRO A 340      25.739  75.830  28.743  1.00 29.60           O  
ATOM   2153  CB  PRO A 340      23.657  73.263  28.459  1.00 30.45           C  
ATOM   2154  CG  PRO A 340      23.328  72.042  27.677  1.00 30.62           C  
ATOM   2155  CD  PRO A 340      24.486  71.808  26.757  1.00 30.50           C  
ATOM   2156  N   ILE A 341      26.729  73.799  28.686  1.00 30.69           N  
ATOM   2157  CA  ILE A 341      27.911  74.203  29.459  1.00 31.15           C  
ATOM   2158  C   ILE A 341      28.740  75.207  28.654  1.00 31.17           C  
ATOM   2159  O   ILE A 341      29.216  76.194  29.217  1.00 32.73           O  
ATOM   2160  CB  ILE A 341      28.776  72.993  29.894  1.00 31.63           C  
ATOM   2161  CG1 ILE A 341      27.949  72.020  30.752  1.00 32.20           C  
ATOM   2162  CG2 ILE A 341      29.988  73.453  30.699  1.00 32.18           C  
ATOM   2163  CD1 ILE A 341      28.667  70.738  31.132  1.00 32.59           C  
ATOM   2164  N   ILE A 342      28.897  74.959  27.349  1.00 30.17           N  
ATOM   2165  CA  ILE A 342      29.595  75.886  26.446  1.00 29.60           C  
ATOM   2166  C   ILE A 342      28.842  77.203  26.326  1.00 31.51           C  
ATOM   2167  O   ILE A 342      29.452  78.269  26.357  1.00 30.52           O  
ATOM   2168  CB  ILE A 342      29.801  75.278  25.035  1.00 28.40           C  
ATOM   2169  CG1 ILE A 342      30.847  74.154  25.096  1.00 28.05           C  
ATOM   2170  CG2 ILE A 342      30.235  76.339  24.019  1.00 27.64           C  
ATOM   2171  CD1 ILE A 342      30.782  73.169  23.948  1.00 27.25           C  
ATOM   2172  N   LEU A 343      27.525  77.121  26.157  1.00 34.98           N  
ATOM   2173  CA  LEU A 343      26.672  78.317  26.077  1.00 37.88           C  
ATOM   2174  C   LEU A 343      26.688  79.130  27.376  1.00 40.53           C  
ATOM   2175  O   LEU A 343      26.580  80.350  27.332  1.00 41.51           O  
ATOM   2176  CB  LEU A 343      25.235  77.947  25.685  1.00 38.02           C  
ATOM   2177  CG  LEU A 343      25.054  77.505  24.224  1.00 37.88           C  
ATOM   2178  CD1 LEU A 343      23.752  76.737  24.047  1.00 38.16           C  
ATOM   2179  CD2 LEU A 343      25.111  78.691  23.270  1.00 37.32           C  
ATOM   2180  N   CYS A 344      26.866  78.455  28.510  1.00 43.49           N  
ATOM   2181  CA  CYS A 344      27.035  79.116  29.815  1.00 47.77           C  
ATOM   2182  C   CYS A 344      28.187  80.130  29.869  1.00 48.59           C  
ATOM   2183  O   CYS A 344      28.081  81.121  30.585  1.00 50.27           O  
ATOM   2184  CB  CYS A 344      27.207  78.067  30.929  1.00 50.78           C  
ATOM   2185  SG  CYS A 344      26.708  78.602  32.581  1.00 55.80           S  
ATOM   2186  N   ARG A 345      29.270  79.888  29.126  1.00 48.79           N  
ATOM   2187  CA  ARG A 345      30.437  80.794  29.107  1.00 48.30           C  
ATOM   2188  C   ARG A 345      30.329  81.951  28.109  1.00 49.01           C  
ATOM   2189  O   ARG A 345      31.172  82.850  28.132  1.00 49.30           O  
ATOM   2190  CB  ARG A 345      31.727  80.019  28.815  1.00 49.53           C  
ATOM   2191  CG  ARG A 345      32.096  78.954  29.836  1.00 50.48           C  
ATOM   2192  CD  ARG A 345      32.530  79.538  31.170  1.00 50.08           C  
ATOM   2193  NE  ARG A 345      32.819  78.474  32.136  1.00 50.38           N  
ATOM   2194  CZ  ARG A 345      34.012  77.918  32.369  1.00 49.78           C  
ATOM   2195  NH1 ARG A 345      35.108  78.305  31.721  1.00 50.73           N  
ATOM   2196  NH2 ARG A 345      34.114  76.953  33.279  1.00 49.65           N  
ATOM   2197  N   SER A 346      29.339  81.924  27.216  1.00 50.42           N  
ATOM   2198  CA  SER A 346      28.994  83.111  26.430  1.00 53.69           C  
ATOM   2199  C   SER A 346      28.430  84.164  27.383  1.00 57.28           C  
ATOM   2200  O   SER A 346      27.697  83.808  28.313  1.00 59.77           O  
ATOM   2201  CB  SER A 346      27.957  82.777  25.366  1.00 54.89           C  
ATOM   2202  OG  SER A 346      28.402  81.703  24.563  1.00 56.57           O  
ATOM   2203  N   PRO A 347      28.762  85.454  27.167  1.00 61.16           N  
ATOM   2204  CA  PRO A 347      28.406  86.513  28.140  1.00 63.37           C  
ATOM   2205  C   PRO A 347      26.892  86.698  28.378  1.00 63.28           C  
ATOM   2206  O   PRO A 347      26.436  86.674  29.526  1.00 61.06           O  
ATOM   2207  CB  PRO A 347      29.028  87.785  27.535  1.00 63.80           C  
ATOM   2208  CG  PRO A 347      29.265  87.479  26.093  1.00 63.45           C  
ATOM   2209  CD  PRO A 347      29.440  85.995  25.973  1.00 62.27           C  
ATOM   2210  N   ASP A 348      26.143  86.870  27.291  1.00 64.37           N  
ATOM   2211  CA  ASP A 348      24.680  87.064  27.334  1.00 64.13           C  
ATOM   2212  C   ASP A 348      23.918  85.880  27.939  1.00 62.17           C  
ATOM   2213  O   ASP A 348      23.002  86.076  28.740  1.00 64.87           O  
ATOM   2214  CB  ASP A 348      24.120  87.410  25.936  1.00 66.18           C  
ATOM   2215  CG  ASP A 348      24.693  86.532  24.818  1.00 69.08           C  
ATOM   2216  OD1 ASP A 348      25.453  85.584  25.113  1.00 71.46           O  
ATOM   2217  OD2 ASP A 348      24.396  86.802  23.636  1.00 72.76           O  
ATOM   2218  N   PHE A 349      24.301  84.664  27.559  1.00 60.64           N  
ATOM   2219  CA  PHE A 349      23.706  83.442  28.124  1.00 59.05           C  
ATOM   2220  C   PHE A 349      24.007  83.258  29.617  1.00 60.54           C  
ATOM   2221  O   PHE A 349      23.178  82.708  30.348  1.00 60.29           O  
ATOM   2222  CB  PHE A 349      24.190  82.201  27.367  1.00 57.96           C  
ATOM   2223  CG  PHE A 349      23.375  81.859  26.152  1.00 56.16           C  
ATOM   2224  CD1 PHE A 349      23.685  82.407  24.910  1.00 55.55           C  
ATOM   2225  CD2 PHE A 349      22.319  80.958  26.241  1.00 54.99           C  
ATOM   2226  CE1 PHE A 349      22.947  82.073  23.783  1.00 55.35           C  
ATOM   2227  CE2 PHE A 349      21.577  80.621  25.120  1.00 54.95           C  
ATOM   2228  CZ  PHE A 349      21.891  81.180  23.889  1.00 55.81           C  
ATOM   2229  N   ARG A 350      25.189  83.697  30.059  1.00 62.51           N  
ATOM   2230  CA  ARG A 350      25.586  83.575  31.470  1.00 65.40           C  
ATOM   2231  C   ARG A 350      24.688  84.417  32.369  1.00 67.46           C  
ATOM   2232  O   ARG A 350      24.188  83.919  33.380  1.00 68.95           O  
ATOM   2233  CB  ARG A 350      27.051  83.981  31.682  1.00 66.31           C  
ATOM   2234  CG  ARG A 350      27.639  83.496  33.001  1.00 66.33           C  
ATOM   2235  CD  ARG A 350      29.158  83.622  33.022  1.00 67.71           C  
ATOM   2236  NE  ARG A 350      29.785  82.778  34.044  1.00 69.58           N  
ATOM   2237  CZ  ARG A 350      29.930  81.451  33.976  1.00 70.49           C  
ATOM   2238  NH1 ARG A 350      29.480  80.754  32.934  1.00 71.26           N  
ATOM   2239  NH2 ARG A 350      30.525  80.803  34.971  1.00 73.62           N  
ATOM   2240  N   LYS A 351      24.487  85.681  31.985  1.00 67.88           N  
ATOM   2241  CA  LYS A 351      23.559  86.589  32.679  1.00 69.80           C  
ATOM   2242  C   LYS A 351      22.166  85.969  32.809  1.00 68.58           C  
ATOM   2243  O   LYS A 351      21.576  85.977  33.892  1.00 68.34           O  
ATOM   2244  CB  LYS A 351      23.441  87.928  31.936  1.00 72.05           C  
ATOM   2245  CG  LYS A 351      24.684  88.804  31.995  1.00 74.36           C  
ATOM   2246  CD  LYS A 351      24.622  89.928  30.968  1.00 75.88           C  
ATOM   2247  CE  LYS A 351      25.983  90.572  30.746  1.00 75.95           C  
ATOM   2248  NZ  LYS A 351      26.879  89.748  29.888  1.00 75.31           N  
ATOM   2249  N   ALA A 352      21.667  85.425  31.697  1.00 66.57           N  
ATOM   2250  CA  ALA A 352      20.339  84.807  31.634  1.00 64.83           C  
ATOM   2251  C   ALA A 352      20.186  83.605  32.565  1.00 64.76           C  
ATOM   2252  O   ALA A 352      19.144  83.460  33.201  1.00 63.77           O  
ATOM   2253  CB  ALA A 352      20.010  84.408  30.203  1.00 64.94           C  
ATOM   2254  N   PHE A 353      21.213  82.752  32.641  1.00 66.51           N  
ATOM   2255  CA  PHE A 353      21.221  81.629  33.600  1.00 67.84           C  
ATOM   2256  C   PHE A 353      21.302  82.119  35.054  1.00 66.44           C  
ATOM   2257  O   PHE A 353      20.719  81.502  35.949  1.00 63.39           O  
ATOM   2258  CB  PHE A 353      22.375  80.639  33.326  1.00 69.42           C  
ATOM   2259  CG  PHE A 353      22.329  79.960  31.969  1.00 69.31           C  
ATOM   2260  CD1 PHE A 353      21.125  79.670  31.325  1.00 69.70           C  
ATOM   2261  CD2 PHE A 353      23.514  79.567  31.350  1.00 69.63           C  
ATOM   2262  CE1 PHE A 353      21.118  79.037  30.089  1.00 69.59           C  
ATOM   2263  CE2 PHE A 353      23.502  78.931  30.114  1.00 68.77           C  
ATOM   2264  CZ  PHE A 353      22.305  78.667  29.485  1.00 67.98           C  
ATOM   2265  N   LYS A 354      22.035  83.213  35.280  1.00 66.82           N  
ATOM   2266  CA  LYS A 354      22.049  83.895  36.577  1.00 66.96           C  
ATOM   2267  C   LYS A 354      20.729  84.633  36.794  1.00 65.32           C  
ATOM   2268  O   LYS A 354      19.855  84.160  37.518  1.00 64.98           O  
ATOM   2269  CB  LYS A 354      23.214  84.889  36.669  1.00 66.95           C  
ATOM   2270  CG  LYS A 354      24.593  84.246  36.683  1.00 68.04           C  
ATOM   2271  CD  LYS A 354      25.702  85.276  36.874  1.00 69.50           C  
ATOM   2272  CE  LYS A 354      25.844  86.208  35.678  1.00 69.79           C  
ATOM   2273  NZ  LYS A 354      27.106  86.999  35.727  1.00 69.84           N  
TER    2274      LYS A 354                                                      
HETATM 2275 NA    NA A 401      16.177  42.380  17.781  1.00 45.23          NA  
HETATM 2276 NA    NA A 402      22.732  66.620  19.169  1.00 48.23          NA  
HETATM 2277  N3  XTK A 501      25.211  52.119   9.997  1.00 18.68           N  
HETATM 2278  C16 XTK A 501      24.893  53.120  10.505  1.00 18.53           C  
HETATM 2279  C1  XTK A 501      24.536  54.295  11.033  1.00 18.29           C  
HETATM 2280  N1  XTK A 501      23.902  55.253  10.328  1.00 18.40           N  
HETATM 2281  C8  XTK A 501      23.669  56.297  11.158  1.00 18.31           C  
HETATM 2282  C7  XTK A 501      23.026  57.624  11.006  1.00 18.47           C  
HETATM 2283  C6  XTK A 501      22.933  58.488  12.091  1.00 18.45           C  
HETATM 2284  C5  XTK A 501      23.429  58.144  13.349  1.00 18.40           C  
HETATM 2285  C2  XTK A 501      24.752  54.611  12.363  1.00 18.44           C  
HETATM 2286  C3  XTK A 501      24.197  55.921  12.485  1.00 18.32           C  
HETATM 2287  C4  XTK A 501      24.050  56.906  13.594  1.00 18.23           C  
HETATM 2288  O1  XTK A 501      24.545  56.565  14.825  1.00 18.11           O  
HETATM 2289  C9  XTK A 501      24.206  57.254  16.029  1.00 18.09           C  
HETATM 2290  C10 XTK A 501      24.384  56.340  17.224  1.00 18.29           C  
HETATM 2291  O2  XTK A 501      24.023  57.083  18.391  1.00 17.53           O  
HETATM 2292  C11 XTK A 501      23.523  55.088  17.041  1.00 18.51           C  
HETATM 2293  N2  XTK A 501      23.428  54.333  18.275  1.00 18.81           N  
HETATM 2294  C12 XTK A 501      22.972  52.948  18.314  1.00 19.05           C  
HETATM 2295  C15 XTK A 501      24.067  52.063  17.704  1.00 19.15           C  
HETATM 2296  C14 XTK A 501      22.683  52.556  19.766  1.00 19.14           C  
HETATM 2297  C13 XTK A 501      21.663  52.839  17.533  1.00 19.48           C  
HETATM 2298  C17 XTK A 501      22.474  58.006   9.670  1.00 18.94           C  
HETATM 2299  N1  MHA A 801       7.762  40.377  22.346  1.00 37.23           N  
HETATM 2300  C1  MHA A 801       8.013  40.131  20.895  1.00 37.26           C  
HETATM 2301  C2  MHA A 801       8.574  41.277  20.060  1.00 37.91           C  
HETATM 2302  O1  MHA A 801       9.004  42.323  20.593  1.00 37.15           O  
HETATM 2303  O2  MHA A 801       8.601  41.130  18.817  1.00 37.26           O  
HETATM 2304  C3  MHA A 801       8.989  40.538  23.161  1.00 38.51           C  
HETATM 2305  C4  MHA A 801       9.569  39.195  23.561  1.00 39.47           C  
HETATM 2306  O3  MHA A 801      10.476  39.194  24.413  1.00 40.35           O  
HETATM 2307  O4  MHA A 801       9.158  38.132  23.048  1.00 40.63           O  
HETATM 2308  C5  MHA A 801       6.805  41.474  22.583  1.00 37.74           C  
HETATM 2309  C6  MHA A 801       5.973  41.328  23.849  1.00 39.21           C  
HETATM 2310  O5  MHA A 801       5.107  42.160  24.072  1.00 40.11           O  
HETATM 2311  N2  MHA A 801       6.176  40.325  24.716  1.00 39.95           N  
HETATM 2312  C18 OLC A2001      43.534  89.951  16.078  1.00 69.01           C  
HETATM 2313  C10 OLC A2001      36.416  85.017  15.409  1.00 56.63           C  
HETATM 2314  C9  OLC A2001      35.197  84.091  15.365  1.00 54.26           C  
HETATM 2315  C17 OLC A2001      42.763  88.750  16.618  1.00 69.09           C  
HETATM 2316  C11 OLC A2001      36.641  85.435  16.850  1.00 60.02           C  
HETATM 2317  C8  OLC A2001      35.081  83.286  14.074  1.00 50.38           C  
HETATM 2318  C16 OLC A2001      41.344  89.133  17.045  1.00 69.43           C  
HETATM 2319  C12 OLC A2001      37.289  86.542  17.222  1.00 64.10           C  
HETATM 2320  C7  OLC A2001      34.613  81.854  14.334  1.00 47.97           C  
HETATM 2321  C15 OLC A2001      40.317  88.149  16.490  1.00 69.83           C  
HETATM 2322  C13 OLC A2001      37.887  87.522  16.234  1.00 66.53           C  
HETATM 2323  C6  OLC A2001      33.760  81.323  13.192  1.00 45.99           C  
HETATM 2324  C14 OLC A2001      38.882  88.465  16.921  1.00 68.15           C  
HETATM 2325  C5  OLC A2001      33.178  79.955  13.521  1.00 43.95           C  
HETATM 2326  C4  OLC A2001      32.113  79.560  12.503  1.00 44.01           C  
HETATM 2327  C3  OLC A2001      30.748  80.145  12.804  1.00 43.21           C  
HETATM 2328  C18 OLC A2002      39.707  69.912  15.818  1.00 56.36           C  
HETATM 2329  C10 OLC A2002      36.046  76.590  13.184  1.00 56.73           C  
HETATM 2330  C9  OLC A2002      36.765  77.499  13.865  1.00 58.63           C  
HETATM 2331  C17 OLC A2002      38.325  70.443  15.481  1.00 55.64           C  
HETATM 2332  C11 OLC A2002      35.448  75.340  13.797  1.00 55.57           C  
HETATM 2333  C8  OLC A2002      37.105  77.427  15.346  1.00 58.52           C  
HETATM 2334  C24 OLC A2002      40.758  85.261  22.932  1.00 79.93           C  
HETATM 2335  C16 OLC A2002      38.103  70.483  13.972  1.00 54.54           C  
HETATM 2336  C12 OLC A2002      35.096  74.319  12.712  1.00 53.76           C  
HETATM 2337  C7  OLC A2002      36.204  78.349  16.163  1.00 58.70           C  
HETATM 2338  C15 OLC A2002      36.674  70.886  13.604  1.00 53.89           C  
HETATM 2339  C13 OLC A2002      35.121  72.880  13.229  1.00 52.58           C  
HETATM 2340  C6  OLC A2002      36.966  79.101  17.244  1.00 58.64           C  
HETATM 2341  C14 OLC A2002      36.540  72.402  13.539  1.00 53.20           C  
HETATM 2342  C5  OLC A2002      37.750  80.289  16.691  1.00 60.72           C  
HETATM 2343  C4  OLC A2002      38.207  81.172  17.843  1.00 63.18           C  
HETATM 2344  C3  OLC A2002      39.017  82.392  17.417  1.00 66.16           C  
HETATM 2345  C2  OLC A2002      39.174  83.325  18.621  1.00 68.99           C  
HETATM 2346  C21 OLC A2002      41.378  83.745  21.037  1.00 76.30           C  
HETATM 2347  C1  OLC A2002      40.524  83.995  18.651  1.00 72.43           C  
HETATM 2348  C22 OLC A2002      40.738  85.082  21.416  1.00 79.09           C  
HETATM 2349  O19 OLC A2002      40.775  84.889  17.865  1.00 76.22           O  
HETATM 2350  O25 OLC A2002      40.079  86.470  23.296  1.00 81.10           O  
HETATM 2351  O23 OLC A2002      41.465  86.148  20.792  1.00 82.79           O  
HETATM 2352  O20 OLC A2002      41.540  83.598  19.621  1.00 74.89           O  
HETATM 2353  C18 OLC A2003      20.382  80.474   0.381  0.50 47.03           C  
HETATM 2354  C10 OLC A2003      28.798  78.560   1.024  0.50 49.81           C  
HETATM 2355  C9  OLC A2003      29.725  79.196  -0.008  0.50 50.85           C  
HETATM 2356  C17 OLC A2003      21.094  79.284  -0.254  0.50 46.99           C  
HETATM 2357  C11 OLC A2003      27.412  79.194   0.993  0.50 48.99           C  
HETATM 2358  C8  OLC A2003      31.089  79.519   0.595  0.50 51.51           C  
HETATM 2359  C16 OLC A2003      22.520  79.647  -0.657  0.50 46.95           C  
HETATM 2360  C12 OLC A2003      27.003  79.473  -0.433  0.50 48.24           C  
HETATM 2361  C7  OLC A2003      32.204  79.324  -0.427  0.50 52.10           C  
HETATM 2362  C15 OLC A2003      23.432  78.425  -0.594  0.50 47.29           C  
HETATM 2363  C13 OLC A2003      25.752  79.256  -0.826  0.50 47.63           C  
HETATM 2364  C6  OLC A2003      32.860  80.652  -0.791  0.50 52.24           C  
HETATM 2365  C14 OLC A2003      24.728  78.729   0.149  0.50 47.39           C  
HETATM 2366  C10 OLC A2004      27.965  87.950  13.489  1.00 48.05           C  
HETATM 2367  C9  OLC A2004      28.011  88.637  12.332  1.00 51.01           C  
HETATM 2368  C11 OLC A2004      26.749  87.186  13.933  1.00 45.33           C  
HETATM 2369  C8  OLC A2004      26.877  88.780  11.325  1.00 51.89           C  
HETATM 2370  C24 OLC A2004      16.560  89.060  15.209  1.00 68.58           C  
HETATM 2371  C12 OLC A2004      26.707  86.778  15.397  1.00 44.67           C  
HETATM 2372  C7  OLC A2004      26.408  90.243  11.290  1.00 53.42           C  
HETATM 2373  C13 OLC A2004      25.249  86.561  15.793  1.00 44.90           C  
HETATM 2374  C6  OLC A2004      25.028  90.461  10.660  1.00 55.56           C  
HETATM 2375  C14 OLC A2004      25.095  85.537  16.905  1.00 45.82           C  
HETATM 2376  C5  OLC A2004      23.974  89.663  11.420  1.00 56.79           C  
HETATM 2377  C4  OLC A2004      22.554  90.213  11.426  1.00 57.63           C  
HETATM 2378  C3  OLC A2004      21.601  89.151  11.981  1.00 60.31           C  
HETATM 2379  C2  OLC A2004      21.888  88.755  13.435  1.00 64.19           C  
HETATM 2380  C21 OLC A2004      18.947  89.084  14.469  1.00 68.65           C  
HETATM 2381  C1  OLC A2004      20.930  87.674  13.885  1.00 67.07           C  
HETATM 2382  C22 OLC A2004      17.497  89.278  14.029  1.00 69.46           C  
HETATM 2383  O19 OLC A2004      21.348  86.594  14.291  1.00 66.09           O  
HETATM 2384  O25 OLC A2004      15.216  89.374  14.833  1.00 67.79           O  
HETATM 2385  O23 OLC A2004      17.310  90.599  13.502  1.00 71.35           O  
HETATM 2386  O20 OLC A2004      19.495  87.923  13.843  1.00 68.15           O  
HETATM 2387  C18 OLC A2005      16.478  58.302   1.001  1.00 48.53           C  
HETATM 2388  C10 OLC A2005      21.068  51.469   1.221  1.00 49.03           C  
HETATM 2389  C9  OLC A2005      20.990  50.172   0.926  1.00 49.64           C  
HETATM 2390  C17 OLC A2005      17.048  57.493   2.144  1.00 48.04           C  
HETATM 2391  C11 OLC A2005      19.867  52.385   1.236  1.00 47.73           C  
HETATM 2392  C8  OLC A2005      19.690  49.495   0.580  1.00 51.04           C  
HETATM 2393  C24 OLC A2005      27.831  42.538   4.369  1.00 58.39           C  
HETATM 2394  C16 OLC A2005      18.577  57.473   2.114  1.00 48.35           C  
HETATM 2395  C12 OLC A2005      20.052  53.465   2.297  1.00 48.55           C  
HETATM 2396  C7  OLC A2005      19.958  48.069   0.136  1.00 52.61           C  
HETATM 2397  C15 OLC A2005      19.141  56.475   3.131  1.00 48.66           C  
HETATM 2398  C13 OLC A2005      20.368  54.811   1.662  1.00 48.54           C  
HETATM 2399  C6  OLC A2005      20.153  47.139   1.327  1.00 53.23           C  
HETATM 2400  C14 OLC A2005      20.494  55.906   2.717  1.00 48.21           C  
HETATM 2401  C5  OLC A2005      20.603  45.751   0.899  1.00 55.31           C  
HETATM 2402  C4  OLC A2005      21.974  45.821   0.244  1.00 56.94           C  
HETATM 2403  C3  OLC A2005      22.914  44.719   0.705  1.00 58.01           C  
HETATM 2404  C2  OLC A2005      24.317  45.161   0.345  1.00 58.28           C  
HETATM 2405  C21 OLC A2005      27.168  44.283   2.758  1.00 54.86           C  
HETATM 2406  C1  OLC A2005      25.334  44.229   0.930  1.00 59.71           C  
HETATM 2407  C22 OLC A2005      26.878  42.874   3.219  1.00 57.02           C  
HETATM 2408  O19 OLC A2005      25.290  43.027   0.716  1.00 62.32           O  
HETATM 2409  O25 OLC A2005      28.016  43.579   5.340  1.00 59.41           O  
HETATM 2410  O23 OLC A2005      25.516  42.754   3.651  1.00 57.79           O  
HETATM 2411  O20 OLC A2005      26.359  44.864   1.742  1.00 54.58           O  
HETATM 2412  O   HOH A3001      22.206  72.679  22.785  1.00 43.86           O  
HETATM 2413  O   HOH A3002      23.064  81.015  12.493  1.00 51.34           O  
HETATM 2414  O   HOH A3003      21.140  65.298  19.682  1.00 37.05           O  
HETATM 2415  O   HOH A3004      24.039  68.796  19.557  1.00 52.53           O  
HETATM 2416  O   HOH A3005      17.250  47.493  27.865  1.00 29.09           O  
HETATM 2417  O   HOH A3006      12.981  43.070  24.605  1.00 24.78           O  
HETATM 2418  O   HOH A3007       8.419  47.223  21.714  1.00 20.38           O  
HETATM 2419  O   HOH A3008       7.531  44.676  20.696  1.00 27.26           O  
HETATM 2420  O   HOH A3009      14.863  44.077  19.396  1.00 33.78           O  
HETATM 2421  O   HOH A3010      21.405  60.620  19.151  1.00 34.52           O  
HETATM 2422  O   HOH A3011      18.204  55.612   8.277  1.00 37.42           O  
HETATM 2423  O   HOH A3012      20.033  57.694   6.618  1.00 54.71           O  
HETATM 2424  O   HOH A3013      14.018  44.368  15.458  1.00 45.52           O  
HETATM 2425  O   HOH A3014      16.651  43.737  15.986  1.00 32.73           O  
HETATM 2426  O   HOH A3015      13.975  41.906  17.180  1.00 45.06           O  
HETATM 2427  O   HOH A3016      21.349  44.519  22.246  1.00 35.60           O  
HETATM 2428  O   HOH A3017      18.582  45.681  15.919  1.00 33.38           O  
HETATM 2429  O   HOH A3018      29.559  55.522   9.799  1.00 34.23           O  
HETATM 2430  O   HOH A3019      31.418  90.011  11.857  1.00 60.80           O  
HETATM 2431  O   HOH A3020      28.907  70.710  20.206  1.00 27.56           O  
HETATM 2432  O   HOH A3021      32.624  59.180  19.078  1.00 20.20           O  
HETATM 2433  O   HOH A3022      24.828  65.658  19.401  1.00 42.25           O  
HETATM 2434  O   HOH A3023      24.495  63.646  21.319  1.00 25.93           O  
HETATM 2435  O   HOH A3024      26.108  70.508  18.628  1.00 49.66           O  
HETATM 2436  O   HOH A3025      22.821  63.158  18.940  1.00 24.14           O  
HETATM 2437  O   HOH A3026       5.238  44.191  22.321  1.00 25.96           O  
CONECT  380 2276                                                                
CONECT  586 1272                                                                
CONECT  692 2276                                                                
CONECT 1218 2275                                                                
CONECT 1220 1266                                                                
CONECT 1245 2275                                                                
CONECT 1264 2275                                                                
CONECT 1266 1220                                                                
CONECT 1272  586                                                                
CONECT 2275 1218 1245 1264 2420                                                 
CONECT 2275 2425 2426                                                           
CONECT 2276  380  692 2414 2415                                                 
CONECT 2276 2433                                                                
CONECT 2277 2278                                                                
CONECT 2278 2277 2279                                                           
CONECT 2279 2278 2280 2285                                                      
CONECT 2280 2279 2281                                                           
CONECT 2281 2280 2282 2286                                                      
CONECT 2282 2281 2283 2298                                                      
CONECT 2283 2282 2284                                                           
CONECT 2284 2283 2287                                                           
CONECT 2285 2279 2286                                                           
CONECT 2286 2281 2285 2287                                                      
CONECT 2287 2284 2286 2288                                                      
CONECT 2288 2287 2289                                                           
CONECT 2289 2288 2290                                                           
CONECT 2290 2289 2291 2292                                                      
CONECT 2291 2290                                                                
CONECT 2292 2290 2293                                                           
CONECT 2293 2292 2294                                                           
CONECT 2294 2293 2295 2296 2297                                                 
CONECT 2295 2294                                                                
CONECT 2296 2294                                                                
CONECT 2297 2294                                                                
CONECT 2298 2282                                                                
CONECT 2299 2300 2304 2308                                                      
CONECT 2300 2299 2301                                                           
CONECT 2301 2300 2302 2303                                                      
CONECT 2302 2301                                                                
CONECT 2303 2301                                                                
CONECT 2304 2299 2305                                                           
CONECT 2305 2304 2306 2307                                                      
CONECT 2306 2305                                                                
CONECT 2307 2305                                                                
CONECT 2308 2299 2309                                                           
CONECT 2309 2308 2310 2311                                                      
CONECT 2310 2309                                                                
CONECT 2311 2309                                                                
CONECT 2312 2315                                                                
CONECT 2313 2314 2316                                                           
CONECT 2314 2313 2317                                                           
CONECT 2315 2312 2318                                                           
CONECT 2316 2313 2319                                                           
CONECT 2317 2314 2320                                                           
CONECT 2318 2315 2321                                                           
CONECT 2319 2316 2322                                                           
CONECT 2320 2317 2323                                                           
CONECT 2321 2318 2324                                                           
CONECT 2322 2319 2324                                                           
CONECT 2323 2320 2325                                                           
CONECT 2324 2321 2322                                                           
CONECT 2325 2323 2326                                                           
CONECT 2326 2325 2327                                                           
CONECT 2327 2326                                                                
CONECT 2328 2331                                                                
CONECT 2329 2330 2332                                                           
CONECT 2330 2329 2333                                                           
CONECT 2331 2328 2335                                                           
CONECT 2332 2329 2336                                                           
CONECT 2333 2330 2337                                                           
CONECT 2334 2348 2350                                                           
CONECT 2335 2331 2338                                                           
CONECT 2336 2332 2339                                                           
CONECT 2337 2333 2340                                                           
CONECT 2338 2335 2341                                                           
CONECT 2339 2336 2341                                                           
CONECT 2340 2337 2342                                                           
CONECT 2341 2338 2339                                                           
CONECT 2342 2340 2343                                                           
CONECT 2343 2342 2344                                                           
CONECT 2344 2343 2345                                                           
CONECT 2345 2344 2347                                                           
CONECT 2346 2348 2352                                                           
CONECT 2347 2345 2349 2352                                                      
CONECT 2348 2334 2346 2351                                                      
CONECT 2349 2347                                                                
CONECT 2350 2334                                                                
CONECT 2351 2348                                                                
CONECT 2352 2346 2347                                                           
CONECT 2353 2356                                                                
CONECT 2354 2355 2357                                                           
CONECT 2355 2354 2358                                                           
CONECT 2356 2353 2359                                                           
CONECT 2357 2354 2360                                                           
CONECT 2358 2355 2361                                                           
CONECT 2359 2356 2362                                                           
CONECT 2360 2357 2363                                                           
CONECT 2361 2358 2364                                                           
CONECT 2362 2359 2365                                                           
CONECT 2363 2360 2365                                                           
CONECT 2364 2361                                                                
CONECT 2365 2362 2363                                                           
CONECT 2366 2367 2368                                                           
CONECT 2367 2366 2369                                                           
CONECT 2368 2366 2371                                                           
CONECT 2369 2367 2372                                                           
CONECT 2370 2382 2384                                                           
CONECT 2371 2368 2373                                                           
CONECT 2372 2369 2374                                                           
CONECT 2373 2371 2375                                                           
CONECT 2374 2372 2376                                                           
CONECT 2375 2373                                                                
CONECT 2376 2374 2377                                                           
CONECT 2377 2376 2378                                                           
CONECT 2378 2377 2379                                                           
CONECT 2379 2378 2381                                                           
CONECT 2380 2382 2386                                                           
CONECT 2381 2379 2383 2386                                                      
CONECT 2382 2370 2380 2385                                                      
CONECT 2383 2381                                                                
CONECT 2384 2370                                                                
CONECT 2385 2382                                                                
CONECT 2386 2380 2381                                                           
CONECT 2387 2390                                                                
CONECT 2388 2389 2391                                                           
CONECT 2389 2388 2392                                                           
CONECT 2390 2387 2394                                                           
CONECT 2391 2388 2395                                                           
CONECT 2392 2389 2396                                                           
CONECT 2393 2407 2409                                                           
CONECT 2394 2390 2397                                                           
CONECT 2395 2391 2398                                                           
CONECT 2396 2392 2399                                                           
CONECT 2397 2394 2400                                                           
CONECT 2398 2395 2400                                                           
CONECT 2399 2396 2401                                                           
CONECT 2400 2397 2398                                                           
CONECT 2401 2399 2402                                                           
CONECT 2402 2401 2403                                                           
CONECT 2403 2402 2404                                                           
CONECT 2404 2403 2406                                                           
CONECT 2405 2407 2411                                                           
CONECT 2406 2404 2408 2411                                                      
CONECT 2407 2393 2405 2410                                                      
CONECT 2408 2406                                                                
CONECT 2409 2393                                                                
CONECT 2410 2407                                                                
CONECT 2411 2405 2406                                                           
CONECT 2414 2276                                                                
CONECT 2415 2276                                                                
CONECT 2420 2275                                                                
CONECT 2425 2275                                                                
CONECT 2426 2275                                                                
CONECT 2433 2276                                                                
MASTER      388    0    9   13    0    0   21    6 2433    1  154   25          
END