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Database: PDB
Entry: 3GP5
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Original site: 3GP5 
HEADER    ISOMERASE                               20-MAR-09   3GP5              
TITLE     CRYSTAL STRUCTURE OF PHOSPHOGLYCEROMUTASE FROM BURKHOLDERIA           
TITLE    2 PSEUDOMALLEI WITH 3-PHOSPHOGLYCERIC ACID AND VANADATE                
COMPND    MOL_ID: 1;                                                            
COMPND   2 MOLECULE: 2,3-BISPHOSPHOGLYCERATE-DEPENDENT PHOSPHOGLYCERATE MUTASE; 
COMPND   3 CHAIN: A, B;                                                         
COMPND   4 SYNONYM: PHOSPHOGLYCEROMUTASE, PGAM, BPG-DEPENDENT PGAM, DPGM;       
COMPND   5 EC: 5.4.2.1;                                                         
COMPND   6 ENGINEERED: YES                                                      
SOURCE    MOL_ID: 1;                                                            
SOURCE   2 ORGANISM_SCIENTIFIC: BURKHOLDERIA PSEUDOMALLEI;                      
SOURCE   3 ORGANISM_COMMON: PSEUDOMONAS PSEUDOMALLEI;                           
SOURCE   4 ORGANISM_TAXID: 28450;                                               
SOURCE   5 STRAIN: 1710B;                                                       
SOURCE   6 GENE: GPMA, BPSL0443;                                                
SOURCE   7 EXPRESSION_SYSTEM: ESCHERICHIA COLI;                                 
SOURCE   8 EXPRESSION_SYSTEM_TAXID: 562;                                        
SOURCE   9 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;                              
SOURCE  10 EXPRESSION_SYSTEM_PLASMID: BG1861                                    
KEYWDS    PHOSPHOGLYCEROMUTASE, DECODE, UWPPG. SBRI, NIAID, SSGCID, GLYCOLYSIS, 
KEYWDS   2 ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER   
KEYWDS   3 FOR INFECTIOUS DISEASE                                               
EXPDTA    X-RAY DIFFRACTION                                                     
AUTHOR    SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE (SSGCID)    
REVDAT   3   05-OCT-11 3GP5    1       JRNL   VERSN                             
REVDAT   2   07-APR-09 3GP5    1       REMARK                                   
REVDAT   1   31-MAR-09 3GP5    0                                                
JRNL        AUTH   D.R.DAVIES,B.L.STAKER,J.A.ABENDROTH,T.E.EDWARDS,R.HARTLEY,   
JRNL        AUTH 2 J.LEONARD,H.KIM,A.L.RYCHEL,S.N.HEWITT,P.J.MYLER,L.J.STEWART  
JRNL        TITL   AN ENSEMBLE OF STRUCTURES OF BURKHOLDERIA PSEUDOMALLEI       
JRNL        TITL 2 2,3-BISPHOSPHOGLYCERATE-DEPENDENT PHOSPHOGLYCERATE MUTASE.   
JRNL        REF    ACTA CRYSTALLOGR.,SECT.F      V.  67  1044 2011              
JRNL        REFN                   ESSN 1744-3091                               
JRNL        PMID   21904048                                                     
JRNL        DOI    10.1107/S1744309111030405                                    
REMARK   2                                                                      
REMARK   2 RESOLUTION.    2.25 ANGSTROMS.                                       
REMARK   3                                                                      
REMARK   3 REFINEMENT.                                                          
REMARK   3   PROGRAM     : REFMAC 5.5.0088                                      
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) : 2.25                           
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 50.00                          
REMARK   3   DATA CUTOFF            (SIGMA(F)) : 0.000                          
REMARK   3   COMPLETENESS FOR RANGE        (%) : 94.2                           
REMARK   3   NUMBER OF REFLECTIONS             : 21960                          
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) : 0.174                           
REMARK   3   R VALUE            (WORKING SET) : 0.171                           
REMARK   3   FREE R VALUE                     : 0.234                           
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 5.100                           
REMARK   3   FREE R VALUE TEST SET COUNT      : 1121                            
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) : 2.25                         
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 2.30                         
REMARK   3   REFLECTION IN BIN     (WORKING SET) : 1210                         
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 74.78                        
REMARK   3   BIN R VALUE           (WORKING SET) : 0.2150                       
REMARK   3   BIN FREE R VALUE SET COUNT          : 77                           
REMARK   3   BIN FREE R VALUE                    : 0.3160                       
REMARK   3                                                                      
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.                    
REMARK   3   PROTEIN ATOMS            : 3771                                    
REMARK   3   NUCLEIC ACID ATOMS       : 0                                       
REMARK   3   HETEROGEN ATOMS          : 73                                      
REMARK   3   SOLVENT ATOMS            : 225                                     
REMARK   3                                                                      
REMARK   3  B VALUES.                                                           
REMARK   3   FROM WILSON PLOT           (A**2) : NULL                           
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 22.90                          
REMARK   3   OVERALL ANISOTROPIC B VALUE.                                       
REMARK   3    B11 (A**2) : 0.55000                                              
REMARK   3    B22 (A**2) : -0.80000                                             
REMARK   3    B33 (A**2) : 0.58000                                              
REMARK   3    B12 (A**2) : 0.17000                                              
REMARK   3    B13 (A**2) : -1.05000                                             
REMARK   3    B23 (A**2) : 0.50000                                              
REMARK   3                                                                      
REMARK   3  ESTIMATED OVERALL COORDINATE ERROR.                                 
REMARK   3   ESU BASED ON R VALUE                            (A): 0.375         
REMARK   3   ESU BASED ON FREE R VALUE                       (A): 0.241         
REMARK   3   ESU BASED ON MAXIMUM LIKELIHOOD                 (A): 0.148         
REMARK   3   ESU FOR B VALUES BASED ON MAXIMUM LIKELIHOOD (A**2): 5.868         
REMARK   3                                                                      
REMARK   3 CORRELATION COEFFICIENTS.                                            
REMARK   3   CORRELATION COEFFICIENT FO-FC      : 0.951                         
REMARK   3   CORRELATION COEFFICIENT FO-FC FREE : 0.913                         
REMARK   3                                                                      
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES        COUNT    RMS    WEIGHT      
REMARK   3   BOND LENGTHS REFINED ATOMS        (A):  3920 ; 0.019 ; 0.022       
REMARK   3   BOND LENGTHS OTHERS               (A):  2657 ; 0.001 ; 0.020       
REMARK   3   BOND ANGLES REFINED ATOMS   (DEGREES):  5327 ; 1.754 ; 1.975       
REMARK   3   BOND ANGLES OTHERS          (DEGREES):  6453 ; 0.973 ; 3.000       
REMARK   3   TORSION ANGLES, PERIOD 1    (DEGREES):   474 ; 7.139 ; 5.000       
REMARK   3   TORSION ANGLES, PERIOD 2    (DEGREES):   179 ;37.877 ;23.408       
REMARK   3   TORSION ANGLES, PERIOD 3    (DEGREES):   621 ;14.811 ;15.000       
REMARK   3   TORSION ANGLES, PERIOD 4    (DEGREES):    32 ;17.728 ;15.000       
REMARK   3   CHIRAL-CENTER RESTRAINTS       (A**3):   582 ; 0.121 ; 0.200       
REMARK   3   GENERAL PLANES REFINED ATOMS      (A):  4314 ; 0.008 ; 0.021       
REMARK   3   GENERAL PLANES OTHERS             (A):   782 ; 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):  2375 ; 0.818 ; 1.500       
REMARK   3   MAIN-CHAIN BOND OTHER ATOMS    (A**2):   953 ; 0.211 ; 1.500       
REMARK   3   MAIN-CHAIN ANGLE REFINED ATOMS (A**2):  3817 ; 1.453 ; 2.000       
REMARK   3   SIDE-CHAIN BOND REFINED ATOMS  (A**2):  1545 ; 2.400 ; 3.000       
REMARK   3   SIDE-CHAIN ANGLE REFINED ATOMS (A**2):  1510 ; 3.694 ; 4.500       
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   : 1.40                                          
REMARK   3   ION PROBE RADIUS   : 0.80                                          
REMARK   3   SHRINKAGE RADIUS   : 0.80                                          
REMARK   3                                                                      
REMARK   3  OTHER REFINEMENT REMARKS:                                           
REMARK   3  HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS                   
REMARK   3   U VALUES      : REFINED INDIVIDUALLY                               
REMARK   4                                                                      
REMARK   4 3GP5 COMPLIES WITH FORMAT V. 3.30, 13-JUL-11                         
REMARK 100                                                                      
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 23-MAR-09.                  
REMARK 100 THE RCSB ID CODE IS RCSB052140.                                      
REMARK 200                                                                      
REMARK 200 EXPERIMENTAL DETAILS                                                 
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION                  
REMARK 200  DATE OF DATA COLLECTION        : 24-OCT-08                          
REMARK 200  TEMPERATURE           (KELVIN) : 100                                
REMARK 200  PH                             : 7.5                                
REMARK 200  NUMBER OF CRYSTALS USED        : 1                                  
REMARK 200                                                                      
REMARK 200  SYNCHROTRON              (Y/N) : N                                  
REMARK 200  RADIATION SOURCE               : ROTATING ANODE                     
REMARK 200  BEAMLINE                       : NULL                               
REMARK 200  X-RAY GENERATOR MODEL          : RIGAKU MICROMAX-007 HF             
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M                                  
REMARK 200  WAVELENGTH OR RANGE        (A) : 1.5418                             
REMARK 200  MONOCHROMATOR                  : NULL                               
REMARK 200  OPTICS                         : NULL                               
REMARK 200                                                                      
REMARK 200  DETECTOR TYPE                  : CCD                                
REMARK 200  DETECTOR MANUFACTURER          : RIGAKU SATURN 944                  
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : HKL2000                            
REMARK 200  DATA SCALING SOFTWARE          : HKL2000                            
REMARK 200                                                                      
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 21960                              
REMARK 200  RESOLUTION RANGE HIGH      (A) : 2.250                              
REMARK 200  RESOLUTION RANGE LOW       (A) : 50.000                             
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : NULL                               
REMARK 200                                                                      
REMARK 200 OVERALL.                                                             
REMARK 200  COMPLETENESS FOR RANGE     (%) : 94.5                               
REMARK 200  DATA REDUNDANCY                : 2.000                              
REMARK 200  R MERGE                    (I) : 0.06800                            
REMARK 200  R SYM                      (I) : NULL                               
REMARK 200  <I/SIGMA(I)> FOR THE DATA SET  : 13.1410                            
REMARK 200                                                                      
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.                                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 2.25                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 2.33                     
REMARK 200  COMPLETENESS FOR SHELL     (%) : 82.1                               
REMARK 200  DATA REDUNDANCY IN SHELL       : 1.90                               
REMARK 200  R MERGE FOR SHELL          (I) : 0.24500                            
REMARK 200  R SYM FOR SHELL            (I) : NULL                               
REMARK 200  <I/SIGMA(I)> FOR SHELL         : 3.452                              
REMARK 200                                                                      
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH                              
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT        
REMARK 200 SOFTWARE USED: MOLREP                                                
REMARK 200 STARTING MODEL: NULL                                                 
REMARK 200                                                                      
REMARK 200 REMARK: NULL                                                         
REMARK 280                                                                      
REMARK 280 CRYSTAL                                                              
REMARK 280 SOLVENT CONTENT, VS   (%): 43.53                                     
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.18                     
REMARK 280                                                                      
REMARK 280 CRYSTALLIZATION CONDITIONS: EMERALD CRYO B-4, 100MM MES PH 7.5, 5%   
REMARK 280  PEG 1000, 10% GLYCEROL, 30% PEG 600, 11.7 MG/ML PROTEIN, VAPOR      
REMARK 280  DIFFUSION, SITTING DROP, TEMPERATURE 289K                           
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY                                            
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 1                              
REMARK 290                                                                      
REMARK 290      SYMOP   SYMMETRY                                                
REMARK 290     NNNMMM   OPERATOR                                                
REMARK 290       1555   X,Y,Z                                                   
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                                                                      
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 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 350                                                                      
REMARK 350 BIOMOLECULE: 2                                                       
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: MONOMERIC                  
REMARK 350 SOFTWARE USED: PISA                                                  
REMARK 350 APPLY THE FOLLOWING TO CHAINS: 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 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    -7                                                      
REMARK 465     ALA A    -6                                                      
REMARK 465     HIS A    -5                                                      
REMARK 465     HIS A    -4                                                      
REMARK 465     HIS A    -3                                                      
REMARK 465     HIS A    -2                                                      
REMARK 465     HIS A    -1                                                      
REMARK 465     HIS A     0                                                      
REMARK 465     ALA A   249                                                      
REMARK 465     MET B    -7                                                      
REMARK 465     ALA B    -6                                                      
REMARK 465     HIS B    -5                                                      
REMARK 465     HIS B    -4                                                      
REMARK 465     HIS B    -3                                                      
REMARK 465     HIS B    -2                                                      
REMARK 465     HIS B    -1                                                      
REMARK 465     HIS B     0                                                      
REMARK 465     ASP B   230                                                      
REMARK 465     GLN B   231                                                      
REMARK 465     GLU B   232                                                      
REMARK 465     ALA B   233                                                      
REMARK 465     ILE B   234                                                      
REMARK 465     ALA B   235                                                      
REMARK 465     LYS B   236                                                      
REMARK 465     ALA B   237                                                      
REMARK 465     GLN B   238                                                      
REMARK 465     ALA B   239                                                      
REMARK 465     ALA B   240                                                      
REMARK 465     VAL B   241                                                      
REMARK 465     ALA B   242                                                      
REMARK 465     GLN B   243                                                      
REMARK 465     GLN B   244                                                      
REMARK 465     GLY B   245                                                      
REMARK 465     LYS B   246                                                      
REMARK 465     SER B   247                                                      
REMARK 465     ALA B   248                                                      
REMARK 465     ALA B   249                                                      
REMARK 470                                                                      
REMARK 470 MISSING ATOM                                                         
REMARK 470 THE FOLLOWING RESIDUES HAVE MISSING ATOMS (M=MODEL NUMBER;           
REMARK 470 RES=RESIDUE NAME; C=CHAIN IDENTIFIER; SSEQ=SEQUENCE NUMBER;          
REMARK 470 I=INSERTION CODE):                                                   
REMARK 470   M RES CSSEQI  ATOMS                                                
REMARK 470     GLU A 129    CG   CD   OE1  OE2                                  
REMARK 470     LYS A 236    CG   CD   CE   NZ                                   
REMARK 470     GLN A 243    CG   CD   OE1  NE2                                  
REMARK 470     GLN A 244    CG   CD   OE1  NE2                                  
REMARK 470     LYS A 246    CG   CD   CE   NZ                                   
REMARK 470     GLU B 129    CG   CD   OE1  OE2                                  
REMARK 470     LYS B 140    CG   CD   CE   NZ                                   
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    ARG B 187   NE  -  CZ  -  NH2 ANGL. DEV. =   3.3 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    GLU A  11      123.74    -39.92                                   
REMARK 500    SER A 166      -54.51   -131.39                                   
REMARK 500    ALA A 181     -132.59   -146.13                                   
REMARK 500    ALA A 242       82.28    -62.49                                   
REMARK 500    GLN A 243       31.62   -141.31                                   
REMARK 500    HIS B   9      153.13    -47.80                                   
REMARK 500    SER B 166      -55.86   -134.49                                   
REMARK 500    ALA B 181     -136.87   -143.09                                   
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     PG6 A  250                                                       
REMARK 610     VO4 A  251                                                       
REMARK 610     VO4 B  252                                                       
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                             VO4 A 251   V                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 3PG A 252   O3                                                     
REMARK 620 2 VO4 A 251   O1  100.6                                              
REMARK 620 3 VO4 A 251   O2  103.0 114.2                                        
REMARK 620 4 VO4 A 251   O4  100.8 111.6 122.4                                  
REMARK 620 5 HIS A   9   NE2 175.2  84.1  75.5  76.6                            
REMARK 620 N                    1     2     3     4                             
REMARK 620                                                                      
REMARK 620 COORDINATION ANGLES FOR:  M RES CSSEQI METAL                         
REMARK 620                             VO4 B 252   V                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 3PG B 253   O3                                                     
REMARK 620 2 VO4 B 252   O2   82.4                                              
REMARK 620 3 VO4 B 252   O3   92.2 118.1                                        
REMARK 620 4 VO4 B 252   O4   86.4 120.2 120.9                                  
REMARK 620 5 HIS B   9   NE2 171.3  96.2  96.0  86.9                            
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 PG6 A 250                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC2                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE VO4 A 251                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC3                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE 3PG A 252                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC4                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE PG4 B 250                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC5                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE PG4 B 251                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC6                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE VO4 B 252                 
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC7                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE 3PG B 253                 
REMARK 900                                                                      
REMARK 900 RELATED ENTRIES                                                      
REMARK 900 RELATED ID: 3EZN   RELATED DB: PDB                                   
REMARK 900 APO STRUCTURE                                                        
REMARK 900 RELATED ID: 3FDZ   RELATED DB: PDB                                   
REMARK 900 STRUCTURE WITH 2,3-DIPHOSPHOGLYCERIC ACID IN ONE MOLECULE            
REMARK 900 AND 3-PHOSPHOGLYCERIC ACID IN THE OTHER                              
REMARK 900 RELATED ID: 3GP3   RELATED DB: PDB                                   
REMARK 900 STRUCTURE WITH 2-PHOSPHOSERINE AND PHOSPHATE                         
REMARK 900 RELATED ID: BUPSA.00114.A   RELATED DB: TARGETDB                     
REMARK 900 RELATED ID: 3GW8   RELATED DB: PDB                                   
DBREF  3GP5 A    1   249  UNP    Q63XU7   GPMA_BURPS       1    249             
DBREF  3GP5 B    1   249  UNP    Q63XU7   GPMA_BURPS       1    249             
SEQADV 3GP5 MET A   -7  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 ALA A   -6  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A   -5  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A   -4  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A   -3  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A   -2  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A   -1  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS A    0  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 MET B   -7  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 ALA B   -6  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B   -5  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B   -4  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B   -3  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B   -2  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B   -1  UNP  Q63XU7              EXPRESSION TAG                 
SEQADV 3GP5 HIS B    0  UNP  Q63XU7              EXPRESSION TAG                 
SEQRES   1 A  257  MET ALA HIS HIS HIS HIS HIS HIS MET TYR LYS LEU VAL          
SEQRES   2 A  257  LEU ILE ARG HIS GLY GLU SER THR TRP ASN LYS GLU ASN          
SEQRES   3 A  257  ARG PHE THR GLY TRP VAL ASP VAL ASP LEU THR GLU GLN          
SEQRES   4 A  257  GLY ASN ARG GLU ALA ARG GLN ALA GLY GLN LEU LEU LYS          
SEQRES   5 A  257  GLU ALA GLY TYR THR PHE ASP ILE ALA TYR THR SER VAL          
SEQRES   6 A  257  LEU LYS ARG ALA ILE ARG THR LEU TRP HIS VAL GLN ASP          
SEQRES   7 A  257  GLN MET ASP LEU MET TYR VAL PRO VAL VAL HIS SER TRP          
SEQRES   8 A  257  ARG LEU ASN GLU ARG HIS TYR GLY ALA LEU SER GLY LEU          
SEQRES   9 A  257  ASN LYS ALA GLU THR ALA ALA LYS TYR GLY ASP GLU GLN          
SEQRES  10 A  257  VAL LEU VAL TRP ARG ARG SER TYR ASP THR PRO PRO PRO          
SEQRES  11 A  257  ALA LEU GLU PRO GLY ASP GLU ARG ALA PRO TYR ALA ASP          
SEQRES  12 A  257  PRO ARG TYR ALA LYS VAL PRO ARG GLU GLN LEU PRO LEU          
SEQRES  13 A  257  THR GLU CYS LEU LYS ASP THR VAL ALA ARG VAL LEU PRO          
SEQRES  14 A  257  LEU TRP ASN GLU SER ILE ALA PRO ALA VAL LYS ALA GLY          
SEQRES  15 A  257  LYS GLN VAL LEU ILE ALA ALA HIS GLY ASN SER LEU ARG          
SEQRES  16 A  257  ALA LEU ILE LYS TYR LEU ASP GLY ILE SER ASP ALA ASP          
SEQRES  17 A  257  ILE VAL GLY LEU ASN ILE PRO ASN GLY VAL PRO LEU VAL          
SEQRES  18 A  257  TYR GLU LEU ASP GLU SER LEU THR PRO ILE ARG HIS TYR          
SEQRES  19 A  257  TYR LEU GLY ASP GLN GLU ALA ILE ALA LYS ALA GLN ALA          
SEQRES  20 A  257  ALA VAL ALA GLN GLN GLY LYS SER ALA ALA                      
SEQRES   1 B  257  MET ALA HIS HIS HIS HIS HIS HIS MET TYR LYS LEU VAL          
SEQRES   2 B  257  LEU ILE ARG HIS GLY GLU SER THR TRP ASN LYS GLU ASN          
SEQRES   3 B  257  ARG PHE THR GLY TRP VAL ASP VAL ASP LEU THR GLU GLN          
SEQRES   4 B  257  GLY ASN ARG GLU ALA ARG GLN ALA GLY GLN LEU LEU LYS          
SEQRES   5 B  257  GLU ALA GLY TYR THR PHE ASP ILE ALA TYR THR SER VAL          
SEQRES   6 B  257  LEU LYS ARG ALA ILE ARG THR LEU TRP HIS VAL GLN ASP          
SEQRES   7 B  257  GLN MET ASP LEU MET TYR VAL PRO VAL VAL HIS SER TRP          
SEQRES   8 B  257  ARG LEU ASN GLU ARG HIS TYR GLY ALA LEU SER GLY LEU          
SEQRES   9 B  257  ASN LYS ALA GLU THR ALA ALA LYS TYR GLY ASP GLU GLN          
SEQRES  10 B  257  VAL LEU VAL TRP ARG ARG SER TYR ASP THR PRO PRO PRO          
SEQRES  11 B  257  ALA LEU GLU PRO GLY ASP GLU ARG ALA PRO TYR ALA ASP          
SEQRES  12 B  257  PRO ARG TYR ALA LYS VAL PRO ARG GLU GLN LEU PRO LEU          
SEQRES  13 B  257  THR GLU CYS LEU LYS ASP THR VAL ALA ARG VAL LEU PRO          
SEQRES  14 B  257  LEU TRP ASN GLU SER ILE ALA PRO ALA VAL LYS ALA GLY          
SEQRES  15 B  257  LYS GLN VAL LEU ILE ALA ALA HIS GLY ASN SER LEU ARG          
SEQRES  16 B  257  ALA LEU ILE LYS TYR LEU ASP GLY ILE SER ASP ALA ASP          
SEQRES  17 B  257  ILE VAL GLY LEU ASN ILE PRO ASN GLY VAL PRO LEU VAL          
SEQRES  18 B  257  TYR GLU LEU ASP GLU SER LEU THR PRO ILE ARG HIS TYR          
SEQRES  19 B  257  TYR LEU GLY ASP GLN GLU ALA ILE ALA LYS ALA GLN ALA          
SEQRES  20 B  257  ALA VAL ALA GLN GLN GLY LYS SER ALA ALA                      
HET    PG6  A 250      17                                                       
HET    VO4  A 251       4                                                       
HET    3PG  A 252      11                                                       
HET    PG4  B 250      13                                                       
HET    PG4  B 251      13                                                       
HET    VO4  B 252       4                                                       
HET    3PG  B 253      11                                                       
HETNAM     PG6 1-(2-METHOXY-ETHOXY)-2-{2-[2-(2-METHOXY-ETHOXY]-                 
HETNAM   2 PG6  ETHOXY}-ETHANE                                                  
HETNAM     VO4 VANADATE ION                                                     
HETNAM     3PG 3-PHOSPHOGLYCERIC ACID                                           
HETNAM     PG4 TETRAETHYLENE GLYCOL                                             
FORMUL   3  PG6    C12 H26 O6                                                   
FORMUL   4  VO4    2(O4 V 3-)                                                   
FORMUL   5  3PG    2(C3 H7 O7 P)                                                
FORMUL   6  PG4    2(C8 H18 O5)                                                 
FORMUL  10  HOH   *225(H2 O)                                                    
HELIX    1   1 SER A   12  GLU A   17  1                                   6    
HELIX    2   2 THR A   29  ALA A   46  1                                  18    
HELIX    3   3 LEU A   58  ASP A   73  1                                  16    
HELIX    4   4 TRP A   83  ASN A   86  5                                   4    
HELIX    5   5 TYR A   90  SER A   94  5                                   5    
HELIX    6   6 ASN A   97  GLY A  106  1                                  10    
HELIX    7   7 GLY A  106  SER A  116  1                                  11    
HELIX    8   8 ASP A  135  ALA A  139  5                                   5    
HELIX    9   9 PRO A  142  LEU A  146  5                                   5    
HELIX   10  10 CYS A  151  SER A  166  1                                  16    
HELIX   11  11 SER A  166  ALA A  173  1                                   8    
HELIX   12  12 HIS A  182  GLY A  195  1                                  14    
HELIX   13  13 ALA A  199  LEU A  204  5                                   6    
HELIX   14  14 ASP A  230  ALA A  242  1                                  13    
HELIX   15  15 SER B   12  GLU B   17  1                                   6    
HELIX   16  16 THR B   29  ALA B   46  1                                  18    
HELIX   17  17 LEU B   58  ASP B   73  1                                  16    
HELIX   18  18 TRP B   83  ASN B   86  5                                   4    
HELIX   19  19 TYR B   90  SER B   94  5                                   5    
HELIX   20  20 ASN B   97  GLY B  106  1                                  10    
HELIX   21  21 GLY B  106  SER B  116  1                                  11    
HELIX   22  22 ASP B  135  ALA B  139  5                                   5    
HELIX   23  23 PRO B  142  LEU B  146  5                                   5    
HELIX   24  24 CYS B  151  SER B  166  1                                  16    
HELIX   25  25 SER B  166  ALA B  173  1                                   8    
HELIX   26  26 HIS B  182  ASP B  194  1                                  13    
HELIX   27  27 ALA B  199  LEU B  204  5                                   6    
SHEET    1   A 6 VAL A  79  HIS A  81  0                                        
SHEET    2   A 6 ILE A  52  THR A  55  1  N  ALA A  53   O  VAL A  80           
SHEET    3   A 6 VAL A 177  ALA A 181  1  O  LEU A 178   N  TYR A  54           
SHEET    4   A 6 TYR A   2  ARG A   8  1  N  ILE A   7   O  ALA A 181           
SHEET    5   A 6 LEU A 212  LEU A 216 -1  O  TYR A 214   N  LEU A   4           
SHEET    6   A 6 PRO A 222  TYR A 227 -1  O  ILE A 223   N  GLU A 215           
SHEET    1   B 6 VAL B  79  HIS B  81  0                                        
SHEET    2   B 6 ILE B  52  THR B  55  1  N  THR B  55   O  VAL B  80           
SHEET    3   B 6 VAL B 177  ALA B 181  1  O  ALA B 180   N  TYR B  54           
SHEET    4   B 6 TYR B   2  ARG B   8  1  N  ILE B   7   O  ALA B 181           
SHEET    5   B 6 LEU B 212  LEU B 216 -1  O  TYR B 214   N  LEU B   4           
SHEET    6   B 6 PRO B 222  TYR B 227 -1  O  ILE B 223   N  GLU B 215           
LINK         V   VO4 A 251                 O3  3PG A 252     1555   1555  1.96  
LINK         V   VO4 B 252                 O3  3PG B 253     1555   1555  2.09  
LINK         NE2 HIS B   9                 V   VO4 B 252     1555   1555  2.18  
LINK         NE2 HIS A   9                 V   VO4 A 251     1555   1555  2.29  
SITE     1 AC1  9 ILE A 190  ASP A 194  ILE A 196  LEU A 204                    
SITE     2 AC1  9 TYR A 214  HIS A 225  TYR A 227  HOH A 336                    
SITE     3 AC1  9 HOH A 337                                                     
SITE     1 AC2  9 ARG A   8  HIS A   9  ASN A  15  ARG A  60                    
SITE     2 AC2  9 GLU A  87  HIS A 182  GLY A 183  3PG A 252                    
SITE     3 AC2  9 HOH A 264                                                     
SITE     1 AC3 13 THR A  21  GLY A  22  GLU A  87  TYR A  90                    
SITE     2 AC3 13 LYS A  98  ARG A 114  ARG A 115  ASN A 184                    
SITE     3 AC3 13 VO4 A 251  HOH A 254  HOH A 265  HOH A 292                    
SITE     4 AC3 13 HOH A 324                                                     
SITE     1 AC4  4 LYS A 140  ASP B  51  ALA B 173  LYS B 175                    
SITE     1 AC5  7 ILE B 190  ASP B 194  ILE B 196  TYR B 214                    
SITE     2 AC5  7 HIS B 225  TYR B 227  HOH B 332                               
SITE     1 AC6  9 ARG B   8  HIS B   9  ASN B  15  ARG B  60                    
SITE     2 AC6  9 GLU B  87  HIS B 182  GLY B 183  3PG B 253                    
SITE     3 AC6  9 HOH B 294                                                     
SITE     1 AC7 11 THR B  21  GLY B  22  GLU B  87  TYR B  90                    
SITE     2 AC7 11 LYS B  98  ARG B 114  ARG B 115  ASN B 184                    
SITE     3 AC7 11 VO4 B 252  HOH B 280  HOH B 295                               
CRYST1   44.749   48.983   62.960 105.46  91.15 107.42 P 1           2          
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      0.022347  0.007010  0.002558        0.00000                         
SCALE2      0.000000  0.021396  0.006381        0.00000                         
SCALE3      0.000000  0.000000  0.016578        0.00000                         
(ATOM LINES ARE NOT SHOWN.)
END                                                                             
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