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LongText Report for: 5ie4-pdb

Name Class
5ie4-pdb
HEADER    HYDROLASE                               25-FEB-16   5IE4              
TITLE     CRYSTAL STRUCTURE OF A LACTONASE MUTANT IN COMPLEX WITH SUBSTRATE A   
COMPND    MOL_ID: 1;                                                            
COMPND   2 MOLECULE: ZEARALENONE HYDROLASE;                                     
COMPND   3 CHAIN: A, B, C;                                                      
COMPND   4 SYNONYM: LACTONASE;                                                  
COMPND   5 ENGINEERED: YES;                                                     
COMPND   6 MUTATION: YES                                                        
SOURCE    MOL_ID: 1;                                                            
SOURCE   2 ORGANISM_SCIENTIFIC: CLONOSTACHYS ROSEA;                             
SOURCE   3 ORGANISM_TAXID: 29856;                                               
SOURCE   4 GENE: ZHD101;                                                        
SOURCE   5 EXPRESSION_SYSTEM: ESCHERICHIA COLI BL21(DE3);                       
SOURCE   6 EXPRESSION_SYSTEM_TAXID: 469008;                                     
SOURCE   7 EXPRESSION_SYSTEM_STRAIN: BL21(DE3);                                 
SOURCE   8 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;                              
SOURCE   9 EXPRESSION_SYSTEM_PLASMID: PET-46 EK/LIC                             
KEYWDS    ALPHA/BETA-HYDROLASE, LACTONASE, ZEARALENONE, HYDROLASE               
EXPDTA    X-RAY DIFFRACTION                                                     
AUTHOR    Y.Y.ZHENG,Z.X.XU,W.D.LIU,C.C.CHEN,R.T.GUO                             
REVDAT   1   04-JAN-17 5IE4    0                                                
JRNL        AUTH   Z.X.XU,W.D.LIU,C.C.CHEN,Q.LI,J.W.HUANG,T.P.KO,G.LIU,W.LIU,   
JRNL        AUTH 2 W.PENG,Y.S.CHENG,Y.CHEN,J.JIN,H.LI,Y.Y.ZHENG,R.T.GUO         
JRNL        TITL   ENHANCED ALPH-ZEARALENOL HYDROLYZING ACTIVITY OF A           
JRNL        TITL 2 MYCOESTROGEN-DETOXIFYING LACTONASE BY STRUCTURE-BASED        
JRNL        TITL 3 ENGINEERING                                                  
JRNL        REF    ACS CATALYSIS                 V.   6  7657 2016              
JRNL        REFN                   ESSN 2155-5435                               
JRNL        DOI    10.1021/ACSCATAL.6B01826                                     
REMARK   2                                                                      
REMARK   2 RESOLUTION.    2.80 ANGSTROMS.                                       
REMARK   3                                                                      
REMARK   3 REFINEMENT.                                                          
REMARK   3   PROGRAM     : REFMAC 5.8.0135                                      
REMARK   3   AUTHORS     : MURSHUDOV,VAGIN,DODSON                               
REMARK   3                                                                      
REMARK   3    REFINEMENT TARGET : MAXIMUM LIKELIHOOD                            
REMARK   3                                                                      
REMARK   3  DATA USED IN REFINEMENT.                                            
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 2.80                           
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 25.00                          
REMARK   3   DATA CUTOFF            (SIGMA(F)) : NULL                           
REMARK   3   COMPLETENESS FOR RANGE        (%) : 97.6                           
REMARK   3   NUMBER OF REFLECTIONS             : 25085                          
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) : 0.206                           
REMARK   3   R VALUE            (WORKING SET) : 0.203                           
REMARK   3   FREE R VALUE                     : 0.265                           
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 4.800                           
REMARK   3   FREE R VALUE TEST SET COUNT      : 1264                            
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) : 2.80                         
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 2.87                         
REMARK   3   REFLECTION IN BIN     (WORKING SET) : 1822                         
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 98.35                        
REMARK   3   BIN R VALUE           (WORKING SET) : 0.2690                       
REMARK   3   BIN FREE R VALUE SET COUNT          : 86                           
REMARK   3   BIN FREE R VALUE                    : 0.3690                       
REMARK   3                                                                      
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.                    
REMARK   3   PROTEIN ATOMS            : 5199                                    
REMARK   3   NUCLEIC ACID ATOMS       : 0                                       
REMARK   3   HETEROGEN ATOMS          : 46                                      
REMARK   3   SOLVENT ATOMS            : 200                                     
REMARK   3                                                                      
REMARK   3  B VALUES.                                                           
REMARK   3   FROM WILSON PLOT           (A**2) : NULL                           
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 36.01                          
REMARK   3   OVERALL ANISOTROPIC B VALUE.                                       
REMARK   3    B11 (A**2) : 1.21000                                              
REMARK   3    B22 (A**2) : 1.21000                                              
REMARK   3    B33 (A**2) : -3.91000                                             
REMARK   3    B12 (A**2) : 0.60000                                              
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): 0.751         
REMARK   3   ESU BASED ON FREE R VALUE                       (A): 0.354         
REMARK   3   ESU BASED ON MAXIMUM LIKELIHOOD                 (A): 0.225         
REMARK   3   ESU FOR B VALUES BASED ON MAXIMUM LIKELIHOOD (A**2): 22.212        
REMARK   3                                                                      
REMARK   3 CORRELATION COEFFICIENTS.                                            
REMARK   3   CORRELATION COEFFICIENT FO-FC      : 0.924                         
REMARK   3   CORRELATION COEFFICIENT FO-FC FREE : 0.875                         
REMARK   3                                                                      
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES        COUNT    RMS    WEIGHT      
REMARK   3   BOND LENGTHS REFINED ATOMS        (A):  5371 ; 0.010 ; 0.019       
REMARK   3   BOND LENGTHS OTHERS               (A):  5054 ; 0.003 ; 0.020       
REMARK   3   BOND ANGLES REFINED ATOMS   (DEGREES):  7321 ; 1.500 ; 1.966       
REMARK   3   BOND ANGLES OTHERS          (DEGREES): 11660 ; 0.969 ; 3.003       
REMARK   3   TORSION ANGLES, PERIOD 1    (DEGREES):   665 ;10.256 ; 5.000       
REMARK   3   TORSION ANGLES, PERIOD 2    (DEGREES):   213 ;37.983 ;24.038       
REMARK   3   TORSION ANGLES, PERIOD 3    (DEGREES):   828 ;21.653 ;15.000       
REMARK   3   TORSION ANGLES, PERIOD 4    (DEGREES):    25 ;18.292 ;15.000       
REMARK   3   CHIRAL-CENTER RESTRAINTS       (A**3):   839 ; 0.099 ; 0.200       
REMARK   3   GENERAL PLANES REFINED ATOMS      (A):  5961 ; 0.017 ; 0.021       
REMARK   3   GENERAL PLANES OTHERS             (A):  1150 ; 0.008 ; 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):  2701 ; 3.832 ; 3.507       
REMARK   3   MAIN-CHAIN BOND OTHER ATOMS    (A**2):  2700 ; 3.832 ; 3.506       
REMARK   3   MAIN-CHAIN ANGLE REFINED ATOMS (A**2):  3353 ; 6.016 ; 5.231       
REMARK   3   MAIN-CHAIN ANGLE OTHER ATOMS   (A**2):  3354 ; 6.015 ; 5.232       
REMARK   3   SIDE-CHAIN BOND REFINED ATOMS  (A**2):  2669 ; 3.499 ; 3.703       
REMARK   3   SIDE-CHAIN BOND OTHER ATOMS    (A**2):  2669 ; 3.497 ; 3.703       
REMARK   3   SIDE-CHAIN ANGLE REFINED ATOMS (A**2):  NULL ;  NULL ;  NULL       
REMARK   3   SIDE-CHAIN ANGLE OTHER ATOMS   (A**2):  3969 ; 5.494 ; 5.469       
REMARK   3   LONG RANGE B REFINED ATOMS     (A**2):  6147 ; 8.694 ;28.019       
REMARK   3   LONG RANGE B OTHER ATOMS       (A**2):  6139 ; 8.697 ;28.005       
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   NCS TYPE: LOCAL                                                    
REMARK   3   NUMBER OF DIFFERENT NCS PAIRS  : 1                                 
REMARK   3  GROUP  CHAIN1    RANGE     CHAIN2     RANGE    COUNT RMS  WEIGHT    
REMARK   3    1     A     1    264       B     1    264   30162  0.12  0.05     
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                                                           
REMARK   4                                                                      
REMARK   4 5IE4 COMPLIES WITH FORMAT V. 3.30, 13-JUL-11                         
REMARK 100                                                                      
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 07-MAR-16.                  
REMARK 100 THE DEPOSITION ID IS D_1000218711.                                   
REMARK 200                                                                      
REMARK 200 EXPERIMENTAL DETAILS                                                 
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION                  
REMARK 200  DATE OF DATA COLLECTION        : 20-JUN-15                          
REMARK 200  TEMPERATURE           (KELVIN) : 100                                
REMARK 200  PH                             : 6.5                                
REMARK 200  NUMBER OF CRYSTALS USED        : 1                                  
REMARK 200                                                                      
REMARK 200  SYNCHROTRON              (Y/N) : Y                                  
REMARK 200  RADIATION SOURCE               : NSRRC                              
REMARK 200  BEAMLINE                       : BL13B1                             
REMARK 200  X-RAY GENERATOR MODEL          : NULL                               
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M                                  
REMARK 200  WAVELENGTH OR RANGE        (A) : 0.97622                            
REMARK 200  MONOCHROMATOR                  : GRAPHITE                           
REMARK 200  OPTICS                         : NULL                               
REMARK 200                                                                      
REMARK 200  DETECTOR TYPE                  : CCD                                
REMARK 200  DETECTOR MANUFACTURER          : ADSC QUANTUM 315R                  
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : HKL-2000                           
REMARK 200  DATA SCALING SOFTWARE          : HKL-2000                           
REMARK 200                                                                      
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 26370                              
REMARK 200  RESOLUTION RANGE HIGH      (A) : 2.800                              
REMARK 200  RESOLUTION RANGE LOW       (A) : 25.000                             
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : NULL                               
REMARK 200                                                                      
REMARK 200 OVERALL.                                                             
REMARK 200  COMPLETENESS FOR RANGE     (%) : 97.5                               
REMARK 200  DATA REDUNDANCY                : 6.200                              
REMARK 200  R MERGE                    (I) : 0.05300                            
REMARK 200  R SYM                      (I) : NULL                               
REMARK 200   FOR THE DATA SET  : 13.9000                            
REMARK 200                                                                      
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.                                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 2.80                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 2.90                     
REMARK 200  COMPLETENESS FOR SHELL     (%) : 98.9                               
REMARK 200  DATA REDUNDANCY IN SHELL       : 6.30                               
REMARK 200  R MERGE FOR SHELL          (I) : 0.16300                            
REMARK 200  R SYM FOR SHELL            (I) : NULL                               
REMARK 200   FOR SHELL         : NULL                               
REMARK 200                                                                      
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH                              
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT        
REMARK 200 SOFTWARE USED: PHASER                                                
REMARK 200 STARTING MODEL: 3WZL                                                 
REMARK 200                                                                      
REMARK 200 REMARK: NULL                                                         
REMARK 280                                                                      
REMARK 280 CRYSTAL                                                              
REMARK 280 SOLVENT CONTENT, VS   (%): 58.18                                     
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.94                     
REMARK 280                                                                      
REMARK 280 CRYSTALLIZATION CONDITIONS: 24% PEG 2000 MME, 0.1M BIS-TRIS, PH      
REMARK 280  6.5, VAPOR DIFFUSION, SITTING DROP, TEMPERATURE 298K                
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY                                            
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 61 2 2                         
REMARK 290                                                                      
REMARK 290      SYMOP   SYMMETRY                                                
REMARK 290     NNNMMM   OPERATOR                                                
REMARK 290       1555   X,Y,Z                                                   
REMARK 290       2555   -Y,X-Y,Z+1/3                                            
REMARK 290       3555   -X+Y,-X,Z+2/3                                           
REMARK 290       4555   -X,-Y,Z+1/2                                             
REMARK 290       5555   Y,-X+Y,Z+5/6                                            
REMARK 290       6555   X-Y,X,Z+1/6                                             
REMARK 290       7555   Y,X,-Z+1/3                                              
REMARK 290       8555   X-Y,-Y,-Z                                               
REMARK 290       9555   -X,-X+Y,-Z+2/3                                          
REMARK 290      10555   -Y,-X,-Z+5/6                                            
REMARK 290      11555   -X+Y,Y,-Z+1/2                                           
REMARK 290      12555   X,X-Y,-Z+1/6                                            
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 -0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   2  0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   2  0.000000  0.000000  1.000000      157.74900            
REMARK 290   SMTRY1   3 -0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   3 -0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   3  0.000000  0.000000  1.000000      315.49800            
REMARK 290   SMTRY1   4 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   4  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   4  0.000000  0.000000  1.000000      236.62350            
REMARK 290   SMTRY1   5  0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   5 -0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   5  0.000000  0.000000  1.000000      394.37250            
REMARK 290   SMTRY1   6  0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   6  0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   6  0.000000  0.000000  1.000000       78.87450            
REMARK 290   SMTRY1   7 -0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   7  0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   7  0.000000  0.000000 -1.000000      157.74900            
REMARK 290   SMTRY1   8  1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   8  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   8  0.000000  0.000000 -1.000000        0.00000            
REMARK 290   SMTRY1   9 -0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   9 -0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   9  0.000000  0.000000 -1.000000      315.49800            
REMARK 290   SMTRY1  10  0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2  10 -0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3  10  0.000000  0.000000 -1.000000      394.37250            
REMARK 290   SMTRY1  11 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2  11  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3  11  0.000000  0.000000 -1.000000      236.62350            
REMARK 290   SMTRY1  12  0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2  12  0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3  12  0.000000  0.000000 -1.000000       78.87450            
REMARK 290                                                                      
REMARK 290 REMARK: NULL                                                         
REMARK 300                                                                      
REMARK 300 BIOMOLECULE: 1, 2                                                    
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: DIMERIC                           
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: DIMERIC                    
REMARK 350 SOFTWARE USED: PISA                                                  
REMARK 350 TOTAL BURIED SURFACE AREA: 1250 ANGSTROM**2                          
REMARK 350 SURFACE AREA OF THE COMPLEX: 20150 ANGSTROM**2                       
REMARK 350 CHANGE IN SOLVENT FREE ENERGY: -13.0 KCAL/MOL                        
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A, B                                  
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 350                                                                      
REMARK 350 BIOMOLECULE: 2                                                       
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: DIMERIC                           
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: DIMERIC                    
REMARK 350 SOFTWARE USED: PISA                                                  
REMARK 350 TOTAL BURIED SURFACE AREA: 1080 ANGSTROM**2                          
REMARK 350 SURFACE AREA OF THE COMPLEX: 17840 ANGSTROM**2                       
REMARK 350 CHANGE IN SOLVENT FREE ENERGY: -9.0 KCAL/MOL                         
REMARK 350 APPLY THE FOLLOWING TO CHAINS: C                                     
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 350   BIOMT1   2  1.000000  0.000000  0.000000        0.00000            
REMARK 350   BIOMT2   2  0.000000 -1.000000  0.000000        0.00000            
REMARK 350   BIOMT3   2  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     THR C     3                                                      
REMARK 465     ARG C     4                                                      
REMARK 465     SER C     5                                                      
REMARK 465     THR C     6                                                      
REMARK 465     ILE C     7                                                      
REMARK 465     SER C     8                                                      
REMARK 465     THR C     9                                                      
REMARK 465     PRO C    10                                                      
REMARK 465     ASN C    11                                                      
REMARK 465     GLY C    12                                                      
REMARK 465     ILE C    13                                                      
REMARK 465     THR C    14                                                      
REMARK 465     LEU C    33                                                      
REMARK 465     GLY C    34                                                      
REMARK 465     GLU C    35                                                      
REMARK 465     PHE C    39                                                      
REMARK 465     ASP C    40                                                      
REMARK 465     SER C    41                                                      
REMARK 465     SER C    42                                                      
REMARK 465     VAL C    43                                                      
REMARK 465     SER C    44                                                      
REMARK 465     GLN C    45                                                      
REMARK 465     ILE C    46                                                      
REMARK 465     ALA C    47                                                      
REMARK 465     THR C    55                                                      
REMARK 465     PHE C    56                                                      
REMARK 465     PRO C    59                                                      
REMARK 465     GLY C    60                                                      
REMARK 465     MET C    61                                                      
REMARK 465     SER C    62                                                      
REMARK 465     ARG C    63                                                      
REMARK 465     SER C    64                                                      
REMARK 465     ALA C    65                                                      
REMARK 465     LYS C    66                                                      
REMARK 465     GLN C    78                                                      
REMARK 465     LYS C    79                                                      
REMARK 465     LEU C    80                                                      
REMARK 465     ASP C    89                                                      
REMARK 465     ALA C    90                                                      
REMARK 465     LEU C   127                                                      
REMARK 465     PRO C   128                                                      
REMARK 465     THR C   129                                                      
REMARK 465     LYS C   130                                                      
REMARK 465     LEU C   131                                                      
REMARK 465     LEU C   132                                                      
REMARK 465     ASP C   133                                                      
REMARK 465     HIS C   134                                                      
REMARK 465     LEU C   135                                                      
REMARK 465     SER C   136                                                      
REMARK 465     ASN C   137                                                      
REMARK 465     THR C   138                                                      
REMARK 465     ALA C   139                                                      
REMARK 465     VAL C   140                                                      
REMARK 465     LEU C   141                                                      
REMARK 465     GLU C   142                                                      
REMARK 465     ASP C   143                                                      
REMARK 465     GLU C   144                                                      
REMARK 465     GLU C   145                                                      
REMARK 465     ILE C   146                                                      
REMARK 465     SER C   147                                                      
REMARK 465     LYS C   148                                                      
REMARK 465     ILE C   149                                                      
REMARK 465     LEU C   150                                                      
REMARK 465     ALA C   151                                                      
REMARK 465     ASN C   152                                                      
REMARK 465     VAL C   153                                                      
REMARK 465     MET C   154                                                      
REMARK 465     LEU C   155                                                      
REMARK 465     ASN C   156                                                      
REMARK 465     ASP C   157                                                      
REMARK 465     VAL C   158                                                      
REMARK 465     SER C   159                                                      
REMARK 465     GLY C   160                                                      
REMARK 465     GLY C   161                                                      
REMARK 465     SER C   162                                                      
REMARK 465     GLU C   163                                                      
REMARK 465     ALA C   164                                                      
REMARK 465     TRP C   165                                                      
REMARK 465     GLN C   166                                                      
REMARK 465     ALA C   167                                                      
REMARK 465     MET C   168                                                      
REMARK 465     GLY C   169                                                      
REMARK 465     ASP C   170                                                      
REMARK 465     GLU C   171                                                      
REMARK 465     VAL C   172                                                      
REMARK 465     HIS C   173                                                      
REMARK 465     ALA C   174                                                      
REMARK 465     ARG C   175                                                      
REMARK 465     LEU C   176                                                      
REMARK 465     HIS C   177                                                      
REMARK 465     LYS C   178                                                      
REMARK 465     ASN C   179                                                      
REMARK 465     TYR C   180                                                      
REMARK 465     PRO C   181                                                      
REMARK 465     VAL C   182                                                      
REMARK 465     TRP C   183                                                      
REMARK 465     ALA C   184                                                      
REMARK 465     ARG C   185                                                      
REMARK 465     GLY C   186                                                      
REMARK 465     TYR C   187                                                      
REMARK 465     PRO C   188                                                      
REMARK 465     ARG C   189                                                      
REMARK 465     THR C   190                                                      
REMARK 465     ILE C   191                                                      
REMARK 465     TRP C   210                                                      
REMARK 465     THR C   211                                                      
REMARK 465     VAL C   212                                                      
REMARK 465     GLY C   213                                                      
REMARK 465     ALA C   214                                                      
REMARK 465     GLU C   219                                                      
REMARK 465     SER C   220                                                      
REMARK 465     ILE C   235                                                      
REMARK 465     GLY C   236                                                      
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: CLOSE CONTACTS IN SAME ASYMMETRIC UNIT                     
REMARK 500                                                                      
REMARK 500 THE FOLLOWING ATOMS ARE IN CLOSE CONTACT.                            
REMARK 500                                                                      
REMARK 500  ATM1  RES C  SSEQI   ATM2  RES C  SSEQI           DISTANCE          
REMARK 500   O    MET C     1     OE1  GLU C    20              2.05            
REMARK 500   O    ALA A    47     O    GLN A    49              2.15            
REMARK 500   O    PRO C    69     OG1  THR C    73              2.19            
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: COVALENT BOND ANGLES                                       
REMARK 500                                                                      
REMARK 500 THE STEREOCHEMICAL PARAMETERS OF THE FOLLOWING RESIDUES              
REMARK 500 HAVE VALUES WHICH DEVIATE FROM EXPECTED VALUES BY MORE               
REMARK 500 THAN 6*RMSD (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN               
REMARK 500 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).                 
REMARK 500                                                                      
REMARK 500 STANDARD TABLE:                                                      
REMARK 500 FORMAT: (10X,I3,1X,A3,1X,A1,I4,A1,3(1X,A4,2X),12X,F5.1)              
REMARK 500                                                                      
REMARK 500 EXPECTED VALUES PROTEIN: ENGH AND HUBER, 1999                        
REMARK 500 EXPECTED VALUES NUCLEIC ACID: CLOWNEY ET AL 1996                     
REMARK 500                                                                      
REMARK 500  M RES CSSEQI ATM1   ATM2   ATM3                                     
REMARK 500    LEU C 237   CA  -  CB  -  CG  ANGL. DEV. =  15.3 DEGREES          
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    SER A  62     -130.56     33.33                                   
REMARK 500    ALA A 102     -130.15     59.75                                   
REMARK 500    GLU A 126       73.38     50.19                                   
REMARK 500    LEU A 132       95.55   -165.44                                   
REMARK 500    ASP A 143     -179.85    -48.67                                   
REMARK 500    GLU A 144      -56.34     75.95                                   
REMARK 500    MET A 241     -108.98   -130.51                                   
REMARK 500    PHE A 243       58.52   -143.96                                   
REMARK 500    SER B  62     -129.40     37.71                                   
REMARK 500    THR B  76      140.33    178.23                                   
REMARK 500    ASP B  92       55.15     34.60                                   
REMARK 500    ALA B 102     -124.97     61.61                                   
REMARK 500    TYR B 115       59.45   -141.39                                   
REMARK 500    GLU B 126       72.91     49.43                                   
REMARK 500    LEU B 132       97.23   -162.88                                   
REMARK 500    LEU B 141       37.61   -155.53                                   
REMARK 500    GLU B 142      125.37     69.75                                   
REMARK 500    MET B 241     -104.45   -124.08                                   
REMARK 500    PHE B 243       58.43   -143.01                                   
REMARK 500    GLU C  20      136.80    172.19                                   
REMARK 500    PRO C  30     -175.50    -67.92                                   
REMARK 500    ASP C  31      -82.67    -91.87                                   
REMARK 500    GLN C  37       16.19    -66.12                                   
REMARK 500    GLN C  49      102.53    177.39                                   
REMARK 500    THR C  76     -146.14   -135.88                                   
REMARK 500    ASP C  92       85.36   -154.75                                   
REMARK 500    ALA C 102     -139.07     52.10                                   
REMARK 500    HIS C 125      107.30   -163.83                                   
REMARK 500    SER C 194       43.37   -108.57                                   
REMARK 500    PRO C 196       49.09    -93.40                                   
REMARK 500    ASN C 224      -46.90    -27.71                                   
REMARK 500    LEU C 238      108.60   -168.54                                   
REMARK 500    MET C 241      -75.36   -157.41                                   
REMARK 500    HIS C 263       42.66   -153.97                                   
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: NON-CIS, NON-TRANS                                         
REMARK 500                                                                      
REMARK 500 THE FOLLOWING PEPTIDE BONDS DEVIATE SIGNIFICANTLY FROM BOTH          
REMARK 500 CIS AND TRANS CONFORMATION.  CIS BONDS, IF ANY, ARE LISTED           
REMARK 500 ON CISPEP RECORDS.  TRANS IS DEFINED AS 180 +/- 30 AND               
REMARK 500 CIS IS DEFINED AS 0 +/- 30 DEGREES.                                  
REMARK 500                                 MODEL     OMEGA                      
REMARK 500 ASP A  157     VAL A  158                 -141.30                    
REMARK 500 VAL B   75     THR B   76                 -149.12                    
REMARK 500 VAL B  140     LEU B  141                 -147.26                    
REMARK 500 ASP B  157     VAL B  158                 -142.85                    
REMARK 500 TRP C   15     TYR C   16                  148.57                    
REMARK 500 GLN C   37     MET C   38                  144.02                    
REMARK 500 GLY C   50     PHE C   51                 -149.52                    
REMARK 500 VAL C   87     LEU C   88                  148.91                    
REMARK 500 ALA C   96     THR C   97                  148.89                    
REMARK 500 THR C  229     LYS C  230                  143.45                    
REMARK 500 PRO C  239     GLY C  240                 -148.79                    
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 525                                                                      
REMARK 525 SOLVENT                                                              
REMARK 525                                                                      
REMARK 525 THE SOLVENT MOLECULES HAVE CHAIN IDENTIFIERS THAT                    
REMARK 525 INDICATE THE POLYMER CHAIN WITH WHICH THEY ARE MOST                  
REMARK 525 CLOSELY ASSOCIATED. THE REMARK LISTS ALL THE SOLVENT                 
REMARK 525 MOLECULES WHICH ARE MORE THAN 5A AWAY FROM THE                       
REMARK 525 NEAREST POLYMER CHAIN (M = MODEL NUMBER;                             
REMARK 525 RES=RESIDUE NAME; C=CHAIN IDENTIFIER; SSEQ=SEQUENCE                  
REMARK 525 NUMBER; I=INSERTION CODE):                                           
REMARK 525                                                                      
REMARK 525  M RES CSSEQI                                                        
REMARK 525    HOH A 464        DISTANCE =  5.92 ANGSTROMS                       
REMARK 525    HOH A 465        DISTANCE =  6.12 ANGSTROMS                       
REMARK 525    HOH A 466        DISTANCE =  6.94 ANGSTROMS                       
REMARK 525    HOH A 467        DISTANCE =  7.25 ANGSTROMS                       
REMARK 525    HOH A 468        DISTANCE =  7.55 ANGSTROMS                       
REMARK 525    HOH A 469        DISTANCE =  8.07 ANGSTROMS                       
REMARK 525    HOH A 470        DISTANCE =  9.04 ANGSTROMS                       
REMARK 525    HOH B 471        DISTANCE =  5.84 ANGSTROMS                       
REMARK 525    HOH B 472        DISTANCE =  5.92 ANGSTROMS                       
REMARK 525    HOH B 473        DISTANCE =  5.94 ANGSTROMS                       
REMARK 525    HOH B 474        DISTANCE =  6.10 ANGSTROMS                       
REMARK 525    HOH B 475        DISTANCE =  6.32 ANGSTROMS                       
REMARK 525    HOH B 476        DISTANCE =  6.84 ANGSTROMS                       
REMARK 525    HOH C 339        DISTANCE =  5.89 ANGSTROMS                       
REMARK 525    HOH C 340        DISTANCE =  6.05 ANGSTROMS                       
REMARK 525    HOH C 341        DISTANCE =  6.16 ANGSTROMS                       
REMARK 525    HOH C 342        DISTANCE =  6.16 ANGSTROMS                       
REMARK 525    HOH C 343        DISTANCE =  6.61 ANGSTROMS                       
REMARK 525    HOH C 344        DISTANCE =  6.78 ANGSTROMS                       
REMARK 525    HOH C 345        DISTANCE =  6.90 ANGSTROMS                       
REMARK 525    HOH C 346        DISTANCE =  6.92 ANGSTROMS                       
REMARK 525    HOH C 347        DISTANCE =  6.94 ANGSTROMS                       
REMARK 525    HOH C 348        DISTANCE =  7.19 ANGSTROMS                       
REMARK 525    HOH C 349        DISTANCE =  7.27 ANGSTROMS                       
REMARK 525    HOH C 350        DISTANCE =  7.52 ANGSTROMS                       
REMARK 525    HOH C 351        DISTANCE =  7.63 ANGSTROMS                       
REMARK 525    HOH C 352        DISTANCE =  8.38 ANGSTROMS                       
REMARK 525    HOH C 353        DISTANCE =  8.54 ANGSTROMS                       
REMARK 525    HOH C 354        DISTANCE =  9.92 ANGSTROMS                       
REMARK 800                                                                      
REMARK 800 SITE                                                                 
REMARK 800 SITE_IDENTIFIER: AC1                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: binding site for residue 36J A 300                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC2                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: binding site for residue 36J B 301                 
REMARK 900                                                                      
REMARK 900 RELATED ENTRIES                                                      
REMARK 900 RELATED ID: 5IE5   RELATED DB: PDB                                   
REMARK 900 RELATED ID: 5IE6   RELATED DB: PDB                                   
REMARK 900 RELATED ID: 5IE7   RELATED DB: PDB                                   
DBREF  5IE4 A    1   264  UNP    Q8NKB0   Q8NKB0_BIOOC     1    264             
DBREF  5IE4 B    1   264  UNP    Q8NKB0   Q8NKB0_BIOOC     1    264             
DBREF  5IE4 C    1   264  UNP    Q8NKB0   Q8NKB0_BIOOC     1    264             
SEQADV 5IE4 ALA A  102  UNP  Q8NKB0    SER   102 ENGINEERED MUTATION            
SEQADV 5IE4 ALA B  102  UNP  Q8NKB0    SER   102 ENGINEERED MUTATION            
SEQADV 5IE4 ALA C  102  UNP  Q8NKB0    SER   102 ENGINEERED MUTATION            
SEQRES   1 A  264  MET ARG THR ARG SER THR ILE SER THR PRO ASN GLY ILE          
SEQRES   2 A  264  THR TRP TYR TYR GLU GLN GLU GLY THR GLY PRO ASP VAL          
SEQRES   3 A  264  VAL LEU VAL PRO ASP GLY LEU GLY GLU CYS GLN MET PHE          
SEQRES   4 A  264  ASP SER SER VAL SER GLN ILE ALA ALA GLN GLY PHE ARG          
SEQRES   5 A  264  VAL THR THR PHE ASP MET PRO GLY MET SER ARG SER ALA          
SEQRES   6 A  264  LYS ALA PRO PRO GLU THR TYR THR GLU VAL THR ALA GLN          
SEQRES   7 A  264  LYS LEU ALA SER TYR VAL ILE SER VAL LEU ASP ALA LEU          
SEQRES   8 A  264  ASP ILE LYS HIS ALA THR VAL TRP GLY CYS ALA SER GLY          
SEQRES   9 A  264  ALA SER THR VAL VAL ALA LEU LEU LEU GLY TYR PRO ASP          
SEQRES  10 A  264  ARG ILE ARG ASN ALA MET CYS HIS GLU LEU PRO THR LYS          
SEQRES  11 A  264  LEU LEU ASP HIS LEU SER ASN THR ALA VAL LEU GLU ASP          
SEQRES  12 A  264  GLU GLU ILE SER LYS ILE LEU ALA ASN VAL MET LEU ASN          
SEQRES  13 A  264  ASP VAL SER GLY GLY SER GLU ALA TRP GLN ALA MET GLY          
SEQRES  14 A  264  ASP GLU VAL HIS ALA ARG LEU HIS LYS ASN TYR PRO VAL          
SEQRES  15 A  264  TRP ALA ARG GLY TYR PRO ARG THR ILE PRO PRO SER ALA          
SEQRES  16 A  264  PRO VAL LYS ASP LEU GLU ALA LEU ARG GLY LYS PRO LEU          
SEQRES  17 A  264  ASP TRP THR VAL GLY ALA ALA THR PRO THR GLU SER PHE          
SEQRES  18 A  264  PHE ASP ASN ILE VAL THR ALA THR LYS ALA GLY VAL ASN          
SEQRES  19 A  264  ILE GLY LEU LEU PRO GLY MET HIS PHE PRO TYR VAL SER          
SEQRES  20 A  264  HIS PRO ASP VAL PHE ALA LYS TYR VAL VAL GLU THR THR          
SEQRES  21 A  264  GLN LYS HIS LEU                                              
SEQRES   1 B  264  MET ARG THR ARG SER THR ILE SER THR PRO ASN GLY ILE          
SEQRES   2 B  264  THR TRP TYR TYR GLU GLN GLU GLY THR GLY PRO ASP VAL          
SEQRES   3 B  264  VAL LEU VAL PRO ASP GLY LEU GLY GLU CYS GLN MET PHE          
SEQRES   4 B  264  ASP SER SER VAL SER GLN ILE ALA ALA GLN GLY PHE ARG          
SEQRES   5 B  264  VAL THR THR PHE ASP MET PRO GLY MET SER ARG SER ALA          
SEQRES   6 B  264  LYS ALA PRO PRO GLU THR TYR THR GLU VAL THR ALA GLN          
SEQRES   7 B  264  LYS LEU ALA SER TYR VAL ILE SER VAL LEU ASP ALA LEU          
SEQRES   8 B  264  ASP ILE LYS HIS ALA THR VAL TRP GLY CYS ALA SER GLY          
SEQRES   9 B  264  ALA SER THR VAL VAL ALA LEU LEU LEU GLY TYR PRO ASP          
SEQRES  10 B  264  ARG ILE ARG ASN ALA MET CYS HIS GLU LEU PRO THR LYS          
SEQRES  11 B  264  LEU LEU ASP HIS LEU SER ASN THR ALA VAL LEU GLU ASP          
SEQRES  12 B  264  GLU GLU ILE SER LYS ILE LEU ALA ASN VAL MET LEU ASN          
SEQRES  13 B  264  ASP VAL SER GLY GLY SER GLU ALA TRP GLN ALA MET GLY          
SEQRES  14 B  264  ASP GLU VAL HIS ALA ARG LEU HIS LYS ASN TYR PRO VAL          
SEQRES  15 B  264  TRP ALA ARG GLY TYR PRO ARG THR ILE PRO PRO SER ALA          
SEQRES  16 B  264  PRO VAL LYS ASP LEU GLU ALA LEU ARG GLY LYS PRO LEU          
SEQRES  17 B  264  ASP TRP THR VAL GLY ALA ALA THR PRO THR GLU SER PHE          
SEQRES  18 B  264  PHE ASP ASN ILE VAL THR ALA THR LYS ALA GLY VAL ASN          
SEQRES  19 B  264  ILE GLY LEU LEU PRO GLY MET HIS PHE PRO TYR VAL SER          
SEQRES  20 B  264  HIS PRO ASP VAL PHE ALA LYS TYR VAL VAL GLU THR THR          
SEQRES  21 B  264  GLN LYS HIS LEU                                              
SEQRES   1 C  264  MET ARG THR ARG SER THR ILE SER THR PRO ASN GLY ILE          
SEQRES   2 C  264  THR TRP TYR TYR GLU GLN GLU GLY THR GLY PRO ASP VAL          
SEQRES   3 C  264  VAL LEU VAL PRO ASP GLY LEU GLY GLU CYS GLN MET PHE          
SEQRES   4 C  264  ASP SER SER VAL SER GLN ILE ALA ALA GLN GLY PHE ARG          
SEQRES   5 C  264  VAL THR THR PHE ASP MET PRO GLY MET SER ARG SER ALA          
SEQRES   6 C  264  LYS ALA PRO PRO GLU THR TYR THR GLU VAL THR ALA GLN          
SEQRES   7 C  264  LYS LEU ALA SER TYR VAL ILE SER VAL LEU ASP ALA LEU          
SEQRES   8 C  264  ASP ILE LYS HIS ALA THR VAL TRP GLY CYS ALA SER GLY          
SEQRES   9 C  264  ALA SER THR VAL VAL ALA LEU LEU LEU GLY TYR PRO ASP          
SEQRES  10 C  264  ARG ILE ARG ASN ALA MET CYS HIS GLU LEU PRO THR LYS          
SEQRES  11 C  264  LEU LEU ASP HIS LEU SER ASN THR ALA VAL LEU GLU ASP          
SEQRES  12 C  264  GLU GLU ILE SER LYS ILE LEU ALA ASN VAL MET LEU ASN          
SEQRES  13 C  264  ASP VAL SER GLY GLY SER GLU ALA TRP GLN ALA MET GLY          
SEQRES  14 C  264  ASP GLU VAL HIS ALA ARG LEU HIS LYS ASN TYR PRO VAL          
SEQRES  15 C  264  TRP ALA ARG GLY TYR PRO ARG THR ILE PRO PRO SER ALA          
SEQRES  16 C  264  PRO VAL LYS ASP LEU GLU ALA LEU ARG GLY LYS PRO LEU          
SEQRES  17 C  264  ASP TRP THR VAL GLY ALA ALA THR PRO THR GLU SER PHE          
SEQRES  18 C  264  PHE ASP ASN ILE VAL THR ALA THR LYS ALA GLY VAL ASN          
SEQRES  19 C  264  ILE GLY LEU LEU PRO GLY MET HIS PHE PRO TYR VAL SER          
SEQRES  20 C  264  HIS PRO ASP VAL PHE ALA LYS TYR VAL VAL GLU THR THR          
SEQRES  21 C  264  GLN LYS HIS LEU                                              
HET    36J  A 300      23                                                       
HET    36J  B 301      23                                                       
HETNAM     36J (3S,7R,11E)-7,14,16-TRIHYDROXY-3-METHYL-3,4,5,6,7,8,9,           
HETNAM   2 36J  10-OCTAHYDRO-1H-2-BENZOXACYCLOTETRADECIN-1-ONE                  
FORMUL   4  36J    2(C18 H24 O5)                                                
FORMUL   6  HOH   *200(H2 O)                                                    
HELIX    1 AA1 GLU A   35  MET A   38  5                                   4    
HELIX    2 AA2 PHE A   39  GLN A   49  1                                  11    
HELIX    3 AA3 MET A   61  ALA A   65  5                                   5    
HELIX    4 AA4 PRO A   68  TYR A   72  5                                   5    
HELIX    5 AA5 THR A   76  LEU A   91  1                                  16    
HELIX    6 AA6 ALA A  102  TYR A  115  1                                  14    
HELIX    7 AA7 LEU A  132  ASN A  137  1                                   6    
HELIX    8 AA8 THR A  138  LEU A  141  5                                   4    
HELIX    9 AA9 GLU A  144  ASP A  157  1                                  14    
HELIX   10 AB1 GLY A  161  MET A  168  1                                   8    
HELIX   11 AB2 GLY A  169  TYR A  187  1                                  19    
HELIX   12 AB3 ILE A  191  ALA A  195  5                                   5    
HELIX   13 AB4 ASP A  199  ARG A  204  1                                   6    
HELIX   14 AB5 PRO A  217  ALA A  231  1                                  15    
HELIX   15 AB6 PHE A  243  HIS A  248  1                                   6    
HELIX   16 AB7 HIS A  248  HIS A  263  1                                  16    
HELIX   17 AB8 GLU B   35  MET B   38  5                                   4    
HELIX   18 AB9 PHE B   39  GLN B   49  1                                  11    
HELIX   19 AC1 MET B   61  ALA B   65  5                                   5    
HELIX   20 AC2 PRO B   68  TYR B   72  5                                   5    
HELIX   21 AC3 THR B   76  LEU B   91  1                                  16    
HELIX   22 AC4 ALA B  102  TYR B  115  1                                  14    
HELIX   23 AC5 LEU B  132  ASN B  137  1                                   6    
HELIX   24 AC6 THR B  138  LEU B  141  5                                   4    
HELIX   25 AC7 GLU B  142  ASP B  157  1                                  16    
HELIX   26 AC8 GLY B  161  MET B  168  1                                   8    
HELIX   27 AC9 GLY B  169  TYR B  187  1                                  19    
HELIX   28 AD1 ASP B  199  ARG B  204  1                                   6    
HELIX   29 AD2 PRO B  217  ALA B  231  1                                  15    
HELIX   30 AD3 PHE B  243  HIS B  248  1                                   6    
HELIX   31 AD4 HIS B  248  HIS B  263  1                                  16    
HELIX   32 AD5 SER C   82  LEU C   88  1                                   7    
HELIX   33 AD6 ALA C  102  TYR C  115  1                                  14    
HELIX   34 AD7 ASP C  199  LEU C  203  5                                   5    
HELIX   35 AD8 ASP C  223  ALA C  228  1                                   6    
HELIX   36 AD9 THR C  229  ALA C  231  5                                   3    
HELIX   37 AE1 PHE C  243  HIS C  248  1                                   6    
HELIX   38 AE2 HIS C  248  LYS C  262  1                                  15    
SHEET    1 AA1 8 THR A   3  THR A   9  0                                        
SHEET    2 AA1 8 ILE A  13  GLU A  20 -1  O  TRP A  15   N  ILE A   7           
SHEET    3 AA1 8 ARG A  52  PHE A  56 -1  O  THR A  55   N  GLU A  18           
SHEET    4 AA1 8 ASP A  25  VAL A  29  1  N  LEU A  28   O  THR A  54           
SHEET    5 AA1 8 ALA A  96  CYS A 101  1  O  THR A  97   N  VAL A  27           
SHEET    6 AA1 8 ILE A 119  HIS A 125  1  O  MET A 123   N  VAL A  98           
SHEET    7 AA1 8 LEU A 208  GLY A 213  1  O  ASP A 209   N  ALA A 122           
SHEET    8 AA1 8 ASN A 234  LEU A 238  1  O  ASN A 234   N  TRP A 210           
SHEET    1 AA2 8 THR B   3  SER B   8  0                                        
SHEET    2 AA2 8 THR B  14  GLU B  20 -1  O  TRP B  15   N  ILE B   7           
SHEET    3 AA2 8 ARG B  52  PHE B  56 -1  O  VAL B  53   N  GLU B  20           
SHEET    4 AA2 8 ASP B  25  VAL B  29  1  N  LEU B  28   O  THR B  54           
SHEET    5 AA2 8 ALA B  96  CYS B 101  1  O  THR B  97   N  VAL B  27           
SHEET    6 AA2 8 ILE B 119  HIS B 125  1  O  MET B 123   N  VAL B  98           
SHEET    7 AA2 8 LEU B 208  GLY B 213  1  O  ASP B 209   N  ALA B 122           
SHEET    8 AA2 8 ASN B 234  LEU B 238  1  O  ASN B 234   N  TRP B 210           
SHEET    1 AA3 6 GLU C  20  GLY C  21  0                                        
SHEET    2 AA3 6 ARG C  52  THR C  54 -1  O  VAL C  53   N  GLU C  20           
SHEET    3 AA3 6 ASP C  25  VAL C  29  1  N  VAL C  26   O  ARG C  52           
SHEET    4 AA3 6 ALA C  96  CYS C 101  1  O  TRP C  99   N  VAL C  29           
SHEET    5 AA3 6 ALA C 122  HIS C 125  1  O  MET C 123   N  GLY C 100           
SHEET    6 AA3 6 LEU C 208  ASP C 209  1  O  ASP C 209   N  CYS C 124           
SITE     1 AC1 13 ASP A  31  GLY A  32  LEU A  33  ALA A 102                    
SITE     2 AC1 13 SER A 103  VAL A 153  MET A 154  VAL A 158                    
SITE     3 AC1 13 TRP A 183  TYR A 187  PRO A 188  ILE A 191                    
SITE     4 AC1 13 PRO A 192                                                     
SITE     1 AC2 15 ASP B  31  GLY B  32  LEU B  33  ALA B 102                    
SITE     2 AC2 15 SER B 103  VAL B 153  MET B 154  VAL B 158                    
SITE     3 AC2 15 TRP B 183  TYR B 187  PRO B 188  ILE B 191                    
SITE     4 AC2 15 PRO B 192  HIS B 242  PHE B 243                               
CRYST1   86.205   86.205  473.247  90.00  90.00 120.00 P 61 2 2     36          
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      0.011600  0.006697  0.000000        0.00000                         
SCALE2      0.000000  0.013395  0.000000        0.00000                         
SCALE3      0.000000  0.000000  0.002113        0.00000                         
TER    2021      LEU A 264                                                      
TER    4042      LEU B 264                                                      
TER    5202      LEU C 264                                                      
MASTER      567    0    2   38   22    0    8    6 5445    3   46   63          
END                                                                             

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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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