GenomeNet

Database: PDB
Entry: 1AR4
LinkDB: 1AR4
Original site: 1AR4 
HEADER    OXIDOREDUCTASE                          09-AUG-97   1AR4              
TITLE     X-RAY STRUCTURE ANALYSIS OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE FROM
TITLE    2 PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN                     
COMPND    MOL_ID: 1;                                                            
COMPND   2 MOLECULE: SUPEROXIDE DISMUTASE;                                      
COMPND   3 CHAIN: A, B;                                                         
COMPND   4 SYNONYM: SOD;                                                        
COMPND   5 EC: 1.15.1.1                                                         
SOURCE    MOL_ID: 1;                                                            
SOURCE   2 ORGANISM_SCIENTIFIC: PROPIONIBACTERIUM FREUDENREICHII SUBSP.         
SOURCE   3 SHERMANII;                                                           
SOURCE   4 ORGANISM_TAXID: 1752;                                                
SOURCE   5 STRAIN: SUBSP. SHERMANII;                                            
SOURCE   6 OTHER_DETAILS: GERMAN COLLECTION OF MICROORGANISMS (DSM)             
KEYWDS    SUPEROXIDE DISMUTASE, OXIDOREDUCTASE, DEGRADES O2-, DISMUTASE         
EXPDTA    X-RAY DIFFRACTION                                                     
AUTHOR    M.SCHMIDT,B.MEIER,F.PARAK                                             
REVDAT   4   16-NOV-11 1AR4    1       HETATM                                   
REVDAT   3   13-JUL-11 1AR4    1       VERSN                                    
REVDAT   2   24-FEB-09 1AR4    1       VERSN                                    
REVDAT   1   12-NOV-97 1AR4    0                                                
JRNL        AUTH   M.SCHMIDT,B.MEIER,F.PARAK                                    
JRNL        TITL   X-RAY STRUCTURE OF THE CAMBIALISTIC SUPEROXIDE DISMUTASE     
JRNL        TITL 2 FROM PROPIONIBACTERIUM SHERMANII ACTIVE WITH FE OR MN        
JRNL        REF    J.BIOL.INORG.CHEM.            V.   1   532 1996              
JRNL        REFN                   ISSN 0949-8257                               
REMARK   2                                                                      
REMARK   2 RESOLUTION.    1.90 ANGSTROMS.                                       
REMARK   3                                                                      
REMARK   3 REFINEMENT.                                                          
REMARK   3   PROGRAM     : X-PLOR 3.1                                           
REMARK   3   AUTHORS     : BRUNGER                                              
REMARK   3                                                                      
REMARK   3  DATA USED IN REFINEMENT.                                            
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 1.90                           
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 9.00                           
REMARK   3   DATA CUTOFF            (SIGMA(F)) : 4.500                          
REMARK   3   DATA CUTOFF HIGH         (ABS(F)) : NULL                           
REMARK   3   DATA CUTOFF LOW          (ABS(F)) : NULL                           
REMARK   3   COMPLETENESS (WORKING+TEST)   (%) : 84.8                           
REMARK   3   NUMBER OF REFLECTIONS             : 24891                          
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 SET) : 0.156                           
REMARK   3   FREE R VALUE                     : 0.205                           
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 10.000                          
REMARK   3   FREE R VALUE TEST SET COUNT      : 2493                            
REMARK   3   ESTIMATED ERROR OF FREE R VALUE  : NULL                            
REMARK   3                                                                      
REMARK   3  FIT IN THE HIGHEST RESOLUTION BIN.                                  
REMARK   3   TOTAL NUMBER OF BINS USED           : 8                            
REMARK   3   BIN RESOLUTION RANGE HIGH       (A) : 1.90                         
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 1.99                         
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 64.30                        
REMARK   3   REFLECTIONS IN BIN    (WORKING SET) : 2093                         
REMARK   3   BIN R VALUE           (WORKING SET) : 0.2060                       
REMARK   3   BIN FREE R VALUE                    : 0.2460                       
REMARK   3   BIN FREE R VALUE TEST SET SIZE  (%) : 9.50                         
REMARK   3   BIN FREE R VALUE TEST SET COUNT     : 220                          
REMARK   3   ESTIMATED ERROR OF BIN FREE R VALUE : NULL                         
REMARK   3                                                                      
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.                    
REMARK   3   PROTEIN ATOMS            : 3210                                    
REMARK   3   NUCLEIC ACID ATOMS       : 0                                       
REMARK   3   HETEROGEN ATOMS          : 2                                       
REMARK   3   SOLVENT ATOMS            : 456                                     
REMARK   3                                                                      
REMARK   3  B VALUES.                                                           
REMARK   3   FROM WILSON PLOT           (A**2) : 16.68                          
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 15.90                          
REMARK   3   OVERALL ANISOTROPIC B VALUE.                                       
REMARK   3    B11 (A**2) : NULL                                                 
REMARK   3    B22 (A**2) : NULL                                                 
REMARK   3    B33 (A**2) : NULL                                                 
REMARK   3    B12 (A**2) : NULL                                                 
REMARK   3    B13 (A**2) : NULL                                                 
REMARK   3    B23 (A**2) : NULL                                                 
REMARK   3                                                                      
REMARK   3  ESTIMATED COORDINATE ERROR.                                         
REMARK   3   ESD FROM LUZZATI PLOT        (A) : NULL                            
REMARK   3   ESD FROM SIGMAA              (A) : 0.18                            
REMARK   3   LOW RESOLUTION CUTOFF        (A) : 5.00                            
REMARK   3                                                                      
REMARK   3  CROSS-VALIDATED ESTIMATED COORDINATE ERROR.                         
REMARK   3   ESD FROM C-V LUZZATI PLOT    (A) : NULL                            
REMARK   3   ESD FROM C-V SIGMAA          (A) : NULL                            
REMARK   3                                                                      
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES.                                   
REMARK   3   BOND LENGTHS                 (A) : 0.005                           
REMARK   3   BOND ANGLES            (DEGREES) : 1.32                            
REMARK   3   DIHEDRAL ANGLES        (DEGREES) : 21.84                           
REMARK   3   IMPROPER ANGLES        (DEGREES) : 0.92                            
REMARK   3                                                                      
REMARK   3  ISOTROPIC THERMAL MODEL : RESTRAINED                                
REMARK   3                                                                      
REMARK   3  ISOTROPIC THERMAL FACTOR RESTRAINTS.    RMS    SIGMA                
REMARK   3   MAIN-CHAIN BOND              (A**2) : 1.500 ; NULL                 
REMARK   3   MAIN-CHAIN ANGLE             (A**2) : 2.000 ; NULL                 
REMARK   3   SIDE-CHAIN BOND              (A**2) : 2.000 ; NULL                 
REMARK   3   SIDE-CHAIN ANGLE             (A**2) : 2.500 ; NULL                 
REMARK   3                                                                      
REMARK   3  NCS MODEL : UNRESTRAINED                                            
REMARK   3                                                                      
REMARK   3  NCS RESTRAINTS.                         RMS   SIGMA/WEIGHT          
REMARK   3   GROUP  1  POSITIONAL            (A) : NULL  ; NULL                 
REMARK   3   GROUP  1  B-FACTOR           (A**2) : NULL  ; NULL                 
REMARK   3                                                                      
REMARK   3  PARAMETER FILE  1  : PARHCSDX.PRO                                   
REMARK   3  PARAMETER FILE  2  : NULL                                           
REMARK   3  PARAMETER FILE  3  : NULL                                           
REMARK   3  TOPOLOGY FILE  1   : TOPHCSDX.PRO                                   
REMARK   3  TOPOLOGY FILE  2   : NULL                                           
REMARK   3  TOPOLOGY FILE  3   : NULL                                           
REMARK   3                                                                      
REMARK   3  OTHER REFINEMENT REMARKS: MN CENTER REFINED WITHOUT VDW AND         
REMARK   3  DISTANCE RESTRAINTS                                                 
REMARK   4                                                                      
REMARK   4 1AR4 COMPLIES WITH FORMAT V. 3.15, 01-DEC-08                         
REMARK 100                                                                      
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY BNL.                                
REMARK 200                                                                      
REMARK 200 EXPERIMENTAL DETAILS                                                 
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION                  
REMARK 200  DATE OF DATA COLLECTION        : DEC-97                             
REMARK 200  TEMPERATURE           (KELVIN) : 295                                
REMARK 200  PH                             : 6.15 (7.4 FOR MICROSEEDS)          
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          : ENRAF-NONIUS FR591                 
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M                                  
REMARK 200  WAVELENGTH OR RANGE        (A) : 1.5418                             
REMARK 200  MONOCHROMATOR                  : GRAPHITE(002)                      
REMARK 200  OPTICS                         : NO                                 
REMARK 200                                                                      
REMARK 200  DETECTOR TYPE                  : AREA DETECTOR                      
REMARK 200  DETECTOR MANUFACTURER          : SIEMENS HI-STAR                    
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : SAINT                              
REMARK 200  DATA SCALING SOFTWARE          : CCP4 (AGROVATA, TRUNCATE)          
REMARK 200                                                                      
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 26323                              
REMARK 200  RESOLUTION RANGE HIGH      (A) : 1.900                              
REMARK 200  RESOLUTION RANGE LOW       (A) : 12.800                             
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : 2.000                              
REMARK 200                                                                      
REMARK 200 OVERALL.                                                             
REMARK 200  COMPLETENESS FOR RANGE     (%) : 89.2                               
REMARK 200  DATA REDUNDANCY                : 3.100                              
REMARK 200  R MERGE                    (I) : 0.04200                            
REMARK 200  R SYM                      (I) : 0.04200                            
REMARK 200  <I/SIGMA(I)> FOR THE DATA SET  : 17.0000                            
REMARK 200                                                                      
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.                                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 1.90                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 1.97                     
REMARK 200  COMPLETENESS FOR SHELL     (%) : 72.3                               
REMARK 200  DATA REDUNDANCY IN SHELL       : 2.30                               
REMARK 200  R MERGE FOR SHELL          (I) : 0.04200                            
REMARK 200  R SYM FOR SHELL            (I) : 0.04200                            
REMARK 200  <I/SIGMA(I)> FOR SHELL         : 5.300                              
REMARK 200                                                                      
REMARK 200 DIFFRACTION PROTOCOL: NULL                                           
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: ISOMORPHOUS WITH FE-SOD OF   
REMARK 200  P.SHERMANII                                                         
REMARK 200 SOFTWARE USED: X-PLOR 3.1                                            
REMARK 200 STARTING MODEL: FE-SOD OF P.SHERMANII                                
REMARK 200                                                                      
REMARK 200 REMARK: NULL                                                         
REMARK 280                                                                      
REMARK 280 CRYSTAL                                                              
REMARK 280 SOLVENT CONTENT, VS   (%): 32.00                                     
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.05                     
REMARK 280                                                                      
REMARK 280 CRYSTALLIZATION CONDITIONS: PROTEIN WAS CRYSTALLIZED AT 50MG/ML      
REMARK 280  FROM 2.15 M (NH4)2SO4, 50 MM KPI, PH 6.15, 4 DEG C, NUCLEATION      
REMARK 280  INDUCED BY MICROSEEDING FROM CRYSTALS GROWN FROM 14MG/ML PROTEIN,   
REMARK 280  2.4 M (NH4)2SO4, 50 MM KPI, PH 7.4, 4 DEG C., MICROSEEDING,         
REMARK 280  TEMPERATURE 277K                                                    
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY                                            
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: C 2 2 21                         
REMARK 290                                                                      
REMARK 290      SYMOP   SYMMETRY                                                
REMARK 290     NNNMMM   OPERATOR                                                
REMARK 290       1555   X,Y,Z                                                   
REMARK 290       2555   -X,-Y,Z+1/2                                             
REMARK 290       3555   -X,Y,-Z+1/2                                             
REMARK 290       4555   X,-Y,-Z                                                 
REMARK 290       5555   X+1/2,Y+1/2,Z                                           
REMARK 290       6555   -X+1/2,-Y+1/2,Z+1/2                                     
REMARK 290       7555   -X+1/2,Y+1/2,-Z+1/2                                     
REMARK 290       8555   X+1/2,-Y+1/2,-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   SMTRY1   2 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   2  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   2  0.000000  0.000000  1.000000       54.42500            
REMARK 290   SMTRY1   3 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   3  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   3  0.000000  0.000000 -1.000000       54.42500            
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        0.00000            
REMARK 290   SMTRY1   5  1.000000  0.000000  0.000000       39.84000            
REMARK 290   SMTRY2   5  0.000000  1.000000  0.000000       42.82000            
REMARK 290   SMTRY3   5  0.000000  0.000000  1.000000        0.00000            
REMARK 290   SMTRY1   6 -1.000000  0.000000  0.000000       39.84000            
REMARK 290   SMTRY2   6  0.000000 -1.000000  0.000000       42.82000            
REMARK 290   SMTRY3   6  0.000000  0.000000  1.000000       54.42500            
REMARK 290   SMTRY1   7 -1.000000  0.000000  0.000000       39.84000            
REMARK 290   SMTRY2   7  0.000000  1.000000  0.000000       42.82000            
REMARK 290   SMTRY3   7  0.000000  0.000000 -1.000000       54.42500            
REMARK 290   SMTRY1   8  1.000000  0.000000  0.000000       39.84000            
REMARK 290   SMTRY2   8  0.000000 -1.000000  0.000000       42.82000            
REMARK 290   SMTRY3   8  0.000000  0.000000 -1.000000        0.00000            
REMARK 290                                                                      
REMARK 290 REMARK: NULL                                                         
REMARK 300                                                                      
REMARK 300 BIOMOLECULE: 1                                                       
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM                
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN                  
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON               
REMARK 300 BURIED SURFACE AREA.                                                 
REMARK 350                                                                      
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN           
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE                
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS          
REMARK 350 GIVEN BELOW.  BOTH NON-CRYSTALLOGRAPHIC AND                          
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.                               
REMARK 350                                                                      
REMARK 350 BIOMOLECULE: 1                                                       
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: TETRAMERIC                        
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: TETRAMERIC                 
REMARK 350 SOFTWARE USED: PISA,PQS                                              
REMARK 350 TOTAL BURIED SURFACE AREA: 12420 ANGSTROM**2                         
REMARK 350 SURFACE AREA OF THE COMPLEX: 28020 ANGSTROM**2                       
REMARK 350 CHANGE IN SOLVENT FREE ENERGY: -54.0 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   BIOMT1   2 -1.000000  0.000000  0.000000       79.68000            
REMARK 350   BIOMT2   2  0.000000  1.000000  0.000000        0.00000            
REMARK 350   BIOMT3   2  0.000000  0.000000 -1.000000       54.42500            
REMARK 375                                                                      
REMARK 375 SPECIAL POSITION                                                     
REMARK 375 THE FOLLOWING ATOMS ARE FOUND TO BE WITHIN 0.15 ANGSTROMS            
REMARK 375 OF A SYMMETRY RELATED ATOM AND ARE ASSUMED TO BE ON SPECIAL          
REMARK 375 POSITIONS.                                                           
REMARK 375                                                                      
REMARK 375 ATOM RES CSSEQI                                                      
REMARK 375      HOH B 314  LIES ON A SPECIAL POSITION.                          
REMARK 375      HOH A 247  LIES ON A SPECIAL POSITION.                          
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: CLOSE CONTACTS                                             
REMARK 500                                                                      
REMARK 500 THE FOLLOWING ATOMS THAT ARE RELATED BY CRYSTALLOGRAPHIC             
REMARK 500 SYMMETRY ARE IN CLOSE CONTACT.  AN ATOM LOCATED WITHIN 0.15          
REMARK 500 ANGSTROMS OF A SYMMETRY RELATED ATOM IS ASSUMED TO BE ON A           
REMARK 500 SPECIAL POSITION AND IS, THEREFORE, LISTED IN REMARK 375             
REMARK 500 INSTEAD OF REMARK 500.  ATOMS WITH NON-BLANK ALTERNATE               
REMARK 500 LOCATION INDICATORS ARE NOT INCLUDED IN THE CALCULATIONS.            
REMARK 500                                                                      
REMARK 500 DISTANCE CUTOFF:                                                     
REMARK 500 2.2 ANGSTROMS FOR CONTACTS NOT INVOLVING HYDROGEN ATOMS              
REMARK 500 1.6 ANGSTROMS FOR CONTACTS INVOLVING HYDROGEN ATOMS                  
REMARK 500                                                                      
REMARK 500  ATM1  RES C  SSEQI   ATM2  RES C  SSEQI  SSYMOP   DISTANCE          
REMARK 500   O    HOH B   266     O    HOH B   266     3655     0.67            
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: COVALENT BOND LENGTHS                                      
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,2(A3,1X,A1,I4,A1,1X,A4,3X),1X,F6.3)               
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   RES CSSEQI ATM2   DEVIATION                     
REMARK 500    GLU B  22   CD    GLU B  22   OE2     0.077                       
REMARK 500    GLU B  25   CD    GLU B  25   OE1     0.080                       
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    LYS A  30      -60.39   -106.00                                   
REMARK 500    ARG A  91      131.55     71.99                                   
REMARK 500    ASP A  94     -128.95     54.79                                   
REMARK 500    ASP A 145     -113.62     59.63                                   
REMARK 500    ASN A 149       46.62     72.67                                   
REMARK 500    PHE A 167      -17.09   -141.35                                   
REMARK 500    LYS A 172     -132.73     55.48                                   
REMARK 500    ARG A 199        8.45    -66.25                                   
REMARK 500    LYS B  30      -62.36    -99.10                                   
REMARK 500    ASP B  94     -141.02     57.26                                   
REMARK 500    ASP B 145     -113.21     58.11                                   
REMARK 500    ASN B 149       46.53     72.47                                   
REMARK 500    PHE B 167      -10.11   -148.68                                   
REMARK 500    LYS B 172     -127.22     57.92                                   
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 278        DISTANCE =  5.76 ANGSTROMS                       
REMARK 525    HOH A 349        DISTANCE =  6.78 ANGSTROMS                       
REMARK 525    HOH A 351        DISTANCE =  5.41 ANGSTROMS                       
REMARK 525    HOH A 360        DISTANCE =  5.80 ANGSTROMS                       
REMARK 525    HOH A 361        DISTANCE =  5.33 ANGSTROMS                       
REMARK 525    HOH A 385        DISTANCE =  7.14 ANGSTROMS                       
REMARK 525    HOH A 386        DISTANCE =  5.31 ANGSTROMS                       
REMARK 525    HOH A 414        DISTANCE =  5.14 ANGSTROMS                       
REMARK 525    HOH A 420        DISTANCE =  5.89 ANGSTROMS                       
REMARK 525    HOH B 347        DISTANCE =  5.24 ANGSTROMS                       
REMARK 525    HOH B 387        DISTANCE =  6.65 ANGSTROMS                       
REMARK 525    HOH B 413        DISTANCE =  6.35 ANGSTROMS                       
REMARK 600                                                                      
REMARK 600 HETEROGEN                                                            
REMARK 600 THE CHARGE OF MANGANESE IS NOT YET KNOWN UNAMBIGUOUSLY.  MN          
REMARK 600 REFINED AS MN+3 BUT MN+2 IS ALSO POSSIBLE.                           
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                              MN A 202  MN                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 HIS A  27   NE2                                                    
REMARK 620 2 HIS A  75   NE2  92.0                                              
REMARK 620 3 ASP A 161   OD2  87.0 110.0                                        
REMARK 620 4 HIS A 165   NE2  96.4 127.1 122.6                                  
REMARK 620 5 HOH A 203   O   170.5  92.0  83.5  88.1                            
REMARK 620 N                    1     2     3     4                             
REMARK 620                                                                      
REMARK 620 COORDINATION ANGLES FOR:  M RES CSSEQI METAL                         
REMARK 620                              MN B 202  MN                            
REMARK 620 N RES CSSEQI ATOM                                                    
REMARK 620 1 HIS B  27   NE2                                                    
REMARK 620 2 HIS B  75   NE2  91.3                                              
REMARK 620 3 ASP B 161   OD2  85.7 104.9                                        
REMARK 620 4 HIS B 165   NE2  92.8 135.5 119.6                                  
REMARK 620 5 HOH B 203   O   169.9  89.9  84.3  93.4                            
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 MN A 202                  
REMARK 800                                                                      
REMARK 800 SITE_IDENTIFIER: AC2                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE MN B 202                  
DBREF  1AR4 A    1   201  UNP    P80293   SODM_PROFR       1    201             
DBREF  1AR4 B    1   201  UNP    P80293   SODM_PROFR       1    201             
SEQRES   1 A  201  ALA VAL TYR THR LEU PRO GLU LEU PRO TYR ASP TYR SER          
SEQRES   2 A  201  ALA LEU GLU PRO TYR ILE SER GLY GLU ILE MET GLU LEU          
SEQRES   3 A  201  HIS HIS ASP LYS HIS HIS LYS ALA TYR VAL ASP GLY ALA          
SEQRES   4 A  201  ASN THR ALA LEU ASP LYS LEU ALA GLU ALA ARG ASP LYS          
SEQRES   5 A  201  ALA ASP PHE GLY ALA ILE ASN LYS LEU GLU LYS ASP LEU          
SEQRES   6 A  201  ALA PHE ASN LEU ALA GLY HIS VAL ASN HIS SER VAL PHE          
SEQRES   7 A  201  TRP LYS ASN MET ALA PRO LYS GLY SER ALA PRO GLU ARG          
SEQRES   8 A  201  PRO THR ASP GLU LEU GLY ALA ALA ILE ASP GLU PHE PHE          
SEQRES   9 A  201  GLY SER PHE ASP ASN MET LYS ALA GLN PHE THR ALA ALA          
SEQRES  10 A  201  ALA THR GLY ILE GLN GLY SER GLY TRP ALA SER LEU VAL          
SEQRES  11 A  201  TRP ASP PRO LEU GLY LYS ARG ILE ASN THR LEU GLN PHE          
SEQRES  12 A  201  TYR ASP HIS GLN ASN ASN LEU PRO ALA GLY SER ILE PRO          
SEQRES  13 A  201  LEU LEU GLN LEU ASP MET TRP GLU HIS ALA PHE TYR LEU          
SEQRES  14 A  201  GLN TYR LYS ASN VAL LYS GLY ASP TYR VAL LYS SER TRP          
SEQRES  15 A  201  TRP ASN VAL VAL ASN TRP ASP ASP VAL ALA LEU ARG PHE          
SEQRES  16 A  201  SER GLU ALA ARG VAL ALA                                      
SEQRES   1 B  201  ALA VAL TYR THR LEU PRO GLU LEU PRO TYR ASP TYR SER          
SEQRES   2 B  201  ALA LEU GLU PRO TYR ILE SER GLY GLU ILE MET GLU LEU          
SEQRES   3 B  201  HIS HIS ASP LYS HIS HIS LYS ALA TYR VAL ASP GLY ALA          
SEQRES   4 B  201  ASN THR ALA LEU ASP LYS LEU ALA GLU ALA ARG ASP LYS          
SEQRES   5 B  201  ALA ASP PHE GLY ALA ILE ASN LYS LEU GLU LYS ASP LEU          
SEQRES   6 B  201  ALA PHE ASN LEU ALA GLY HIS VAL ASN HIS SER VAL PHE          
SEQRES   7 B  201  TRP LYS ASN MET ALA PRO LYS GLY SER ALA PRO GLU ARG          
SEQRES   8 B  201  PRO THR ASP GLU LEU GLY ALA ALA ILE ASP GLU PHE PHE          
SEQRES   9 B  201  GLY SER PHE ASP ASN MET LYS ALA GLN PHE THR ALA ALA          
SEQRES  10 B  201  ALA THR GLY ILE GLN GLY SER GLY TRP ALA SER LEU VAL          
SEQRES  11 B  201  TRP ASP PRO LEU GLY LYS ARG ILE ASN THR LEU GLN PHE          
SEQRES  12 B  201  TYR ASP HIS GLN ASN ASN LEU PRO ALA GLY SER ILE PRO          
SEQRES  13 B  201  LEU LEU GLN LEU ASP MET TRP GLU HIS ALA PHE TYR LEU          
SEQRES  14 B  201  GLN TYR LYS ASN VAL LYS GLY ASP TYR VAL LYS SER TRP          
SEQRES  15 B  201  TRP ASN VAL VAL ASN TRP ASP ASP VAL ALA LEU ARG PHE          
SEQRES  16 B  201  SER GLU ALA ARG VAL ALA                                      
HET     MN  A 202       1                                                       
HET     MN  B 202       1                                                       
HETNAM      MN MANGANESE (II) ION                                               
FORMUL   3   MN    2(MN 2+)                                                     
FORMUL   5  HOH   *456(H2 O)                                                    
HELIX    1   1 GLY A   21  ASP A   51  1                                  31    
HELIX    2   3 ILE A   58  LYS A   80  1                                  23    
HELIX    3   4 ASP A   94  PHE A  104  1                                  11    
HELIX    4   5 PHE A  107  THR A  119  1                                  13    
HELIX    5   6 GLU A  164  TYR A  171  1                                   8    
HELIX    6   8 LYS A  175  VAL A  185  1                                  11    
HELIX    7   9 TRP A  188  ALA A  198  1                                  11    
HELIX    8  10 GLY B   21  ASP B   51  1                                  31    
HELIX    9  12 ILE B   58  LYS B   80  1                                  23    
HELIX   10  13 ASP B   94  PHE B  104  1                                  11    
HELIX   11  14 PHE B  107  THR B  119  1                                  13    
HELIX   12  15 GLU B  164  TYR B  171  1                                   8    
HELIX   13  17 LYS B  175  VAL B  185  1                                  11    
HELIX   14  18 TRP B  188  ALA B  198  1                                  11    
SHEET    1   A 3 ARG A 137  TYR A 144  0                                        
SHEET    2   A 3 GLY A 125  ASP A 132 -1  N  ASP A 132   O  ARG A 137           
SHEET    3   A 3 ILE A 155  ASP A 161 -1  N  LEU A 160   O  ALA A 127           
SHEET    1   B 3 ARG B 137  TYR B 144  0                                        
SHEET    2   B 3 GLY B 125  ASP B 132 -1  N  ASP B 132   O  ARG B 137           
SHEET    3   B 3 ILE B 155  ASP B 161 -1  N  LEU B 160   O  ALA B 127           
LINK        MN    MN A 202                 NE2 HIS A  27     1555   1555  2.14  
LINK        MN    MN A 202                 NE2 HIS A  75     1555   1555  2.19  
LINK        MN    MN A 202                 OD2 ASP A 161     1555   1555  1.91  
LINK        MN    MN A 202                 NE2 HIS A 165     1555   1555  2.24  
LINK        MN    MN A 202                 O   HOH A 203     1555   1555  2.25  
LINK        MN    MN B 202                 NE2 HIS B  27     1555   1555  2.17  
LINK        MN    MN B 202                 NE2 HIS B  75     1555   1555  2.13  
LINK        MN    MN B 202                 OD2 ASP B 161     1555   1555  1.91  
LINK        MN    MN B 202                 NE2 HIS B 165     1555   1555  2.13  
LINK        MN    MN B 202                 O   HOH B 203     1555   1555  2.34  
CISPEP   1 GLU A   16    PRO A   17          0         0.69                     
CISPEP   2 GLU B   16    PRO B   17          0         0.19                     
SITE     1 AC1  5 HIS A  27  HIS A  75  ASP A 161  HIS A 165                    
SITE     2 AC1  5 HOH A 203                                                     
SITE     1 AC2  5 HIS B  27  HIS B  75  ASP B 161  HIS B 165                    
SITE     2 AC2  5 HOH B 203                                                     
CRYST1   79.680   85.640  108.850  90.00  90.00  90.00 C 2 2 21     16          
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      0.012550  0.000000  0.000000        0.00000                         
SCALE2      0.000000  0.011677  0.000000        0.00000                         
SCALE3      0.000000  0.000000  0.009187        0.00000                         
MTRIX1   1  0.203600 -0.000300 -0.979100       58.36490    1                    
MTRIX2   1  0.003500 -1.000000  0.001000       33.06150    1                    
MTRIX3   1 -0.979000 -0.003600 -0.203600       71.76470    1                    
(ATOM LINES ARE NOT SHOWN.)
END                                                                             
DBGET integrated database retrieval system