Header list of 1zwm.pdb file
Complete list - r 2 2 Bytes
HEADER STRUCTURAL PROTEIN 03-JUN-05 1ZWM
TITLE NMR STRUCTURE OF MURINE GAMMA-S CRYSTALLIN
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: GAMMA CRYSTALLIN S;
COMPND 3 CHAIN: A;
COMPND 4 SYNONYM: GAMMA CRYSTALLIN S;
COMPND 5 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: MUS MUSCULUS;
SOURCE 3 ORGANISM_COMMON: HOUSE MOUSE;
SOURCE 4 ORGANISM_TAXID: 10090;
SOURCE 5 GENE: CRYGS;
SOURCE 6 EXPRESSION_SYSTEM: ESCHERICHIA COLI BL21;
SOURCE 7 EXPRESSION_SYSTEM_TAXID: 511693;
SOURCE 8 EXPRESSION_SYSTEM_STRAIN: BL21
KEYWDS ALIGNMENT, DEUTERATION, LIQUID CRYSTAL, PF1, RELAXATION, RDC,
KEYWDS 2 RESIDUAL DIPOLAR COUPLING, MOLECULAR FRAGMENT REPLACEMENT, MFR,
KEYWDS 3 STRUCTURAL PROTEIN
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR Z.WU,F.DELAGLIO,K.WYATT,G.WISTOW,A.BAX
REVDAT 4 02-MAR-22 1ZWM 1 REMARK
REVDAT 3 24-FEB-09 1ZWM 1 VERSN
REVDAT 2 27-DEC-05 1ZWM 1 JRNL
REVDAT 1 05-JUL-05 1ZWM 0
JRNL AUTH Z.WU,F.DELAGLIO,K.WYATT,G.WISTOW,A.BAX
JRNL TITL SOLUTION STRUCTURE OF (GAMMA)S-CRYSTALLIN BY MOLECULAR
JRNL TITL 2 FRAGMENT REPLACEMENT NMR.
JRNL REF PROTEIN SCI. V. 14 3101 2005
JRNL REFN ISSN 0961-8368
JRNL PMID 16260758
JRNL DOI 10.1110/PS.051635205
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : NMRPIPE 1.0, DYNAMO 3.1, X-PLOR 2.9.4
REMARK 3 AUTHORS : DELAGLIO, GRZESIEK, ZHU, VUISTER, PFEIFER, BAX
REMARK 3 (NMRPIPE), DELAGLIO, KUSZEWSKI (DYNAMO), BRUNGER,
REMARK 3 SCHWIETERS, KUSZEWSKI, TJANDRA, CLORE (X-PLOR)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS:
REMARK 3 SIMULATED ANNEALING, INCLUDING A H-BOND POTENTIAL OF MEAN FORCE,
REMARK 3 H-BOND PAIRING WAS DETERMINED AUTOMATICALLY, NO EXPLICIT H-BOND
REMARK 3 PAIRING RESTRAINTS WERE USED; TIGHT BACKBONE TORSION ANGLE
REMARK 3 RESTRAINTS ARE DERIVED FROM A SEARCH THROUGH THE RCSB FOR
REMARK 3 FRAGMENTS THAT MATCH EXPERIMENTAL DIPOLAR COUPLINGS
REMARK 4
REMARK 4 1ZWM COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 06-JUN-05.
REMARK 100 THE DEPOSITION ID IS D_1000033202.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 298
REMARK 210 PH : 6.0
REMARK 210 IONIC STRENGTH : 25 MM IMIDAZOLE, 10 MM KCL,
REMARK 210 0.04% NAN3
REMARK 210 PRESSURE : 1 ATM
REMARK 210 SAMPLE CONTENTS : 0.7-1.5 MM GS, 25 MM IMIDAZOLE,
REMARK 210 PH 6.0, 10 MM KCL, 0.04% NAN3.
REMARK 210 DIPOLAR COUPLINGS MEASURED IN 2H/
REMARK 210 15N/13C GAMMAS, IN STRETCHED
REMARK 210 POLYACRYLAMIDE GEL, AND IN 3 MG/
REMARK 210 ML PF1 (GELLED), 120 MM KCL; 90%
REMARK 210 H2O, 10% D2O
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : NULL
REMARK 210 SPECTROMETER FIELD STRENGTH : 600 MHZ
REMARK 210 SPECTROMETER MODEL : DRX600 WITH PFG-CRYOPROBE
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NULL
REMARK 210 METHOD USED : MFR FOLLOWED BY SIMULATED
REMARK 210 ANNEALING
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 20
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 20
REMARK 210 CONFORMERS, SELECTION CRITERIA : ALL CALCULATED STRUCTURES
REMARK 210 SUBMITTED
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 12
REMARK 210
REMARK 210 REMARK: THE STRUCTURE WAS DETERMINED USING TRIPLE-RESONANCE NMR
REMARK 210 SPECTROSCOPY.
REMARK 215
REMARK 215 NMR STUDY
REMARK 215 THE COORDINATES IN THIS ENTRY WERE GENERATED FROM SOLUTION
REMARK 215 NMR DATA. PROTEIN DATA BANK CONVENTIONS REQUIRE THAT
REMARK 215 CRYST1 AND SCALE RECORDS BE INCLUDED, BUT THE VALUES ON
REMARK 215 THESE RECORDS ARE MEANINGLESS.
REMARK 300
REMARK 300 BIOMOLECULE: 1
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON
REMARK 300 BURIED SURFACE AREA.
REMARK 350
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS
REMARK 350 GIVEN BELOW. BOTH NON-CRYSTALLOGRAPHIC AND
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.
REMARK 350
REMARK 350 BIOMOLECULE: 1
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: MONOMERIC
REMARK 350 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 470
REMARK 470 MISSING ATOM
REMARK 470 THE FOLLOWING RESIDUES HAVE MISSING ATOMS (RES=RESIDUE NAME;
REMARK 470 C=CHAIN IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE):
REMARK 470 MODELS 1-20
REMARK 470 RES CSSEQI ATOMS
REMARK 470 GLU A 177 O
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: CLOSE CONTACTS
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
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 1 SER A 89 -154.18 -103.88
REMARK 500 1 GLU A 133 -75.34 -147.08
REMARK 500 1 ASP A 152 -124.77 -104.68
REMARK 500 1 LYS A 154 -167.20 -115.37
REMARK 500 2 GLU A 133 -75.31 -146.19
REMARK 500 2 ASP A 152 -124.40 -104.23
REMARK 500 3 SER A 89 -154.33 -104.32
REMARK 500 3 GLU A 133 -77.78 -145.07
REMARK 500 3 ASP A 152 -110.26 -104.56
REMARK 500 3 LYS A 153 51.68 -156.50
REMARK 500 3 LYS A 154 -163.08 -112.71
REMARK 500 4 SER A 89 -154.58 -104.41
REMARK 500 4 GLU A 133 -80.65 -145.65
REMARK 500 4 ASP A 152 -166.41 -106.73
REMARK 500 4 LYS A 153 52.85 -90.68
REMARK 500 5 GLU A 133 -76.58 -146.66
REMARK 500 5 ASP A 152 -96.96 -109.91
REMARK 500 5 LYS A 153 51.55 -176.37
REMARK 500 5 LYS A 154 -159.77 -113.82
REMARK 500 6 SER A 89 -154.17 -104.34
REMARK 500 6 CYS A 129 145.25 -170.41
REMARK 500 6 GLU A 133 -74.73 -146.03
REMARK 500 6 PRO A 142 170.02 -55.16
REMARK 500 6 ASP A 152 -116.15 -103.06
REMARK 500 6 LYS A 153 49.69 -157.78
REMARK 500 6 LYS A 154 -162.97 -113.64
REMARK 500 7 SER A 89 -154.66 -103.94
REMARK 500 7 CYS A 129 148.81 -170.14
REMARK 500 7 GLU A 133 -75.99 -147.71
REMARK 500 7 ASP A 152 -111.65 -109.34
REMARK 500 7 LYS A 153 45.55 -168.81
REMARK 500 7 LYS A 154 -153.77 -113.59
REMARK 500 8 GLU A 133 -158.17 -161.36
REMARK 500 8 ASP A 152 -126.18 -111.32
REMARK 500 9 LYS A 2 23.45 -76.40
REMARK 500 9 SER A 89 -154.89 -103.56
REMARK 500 9 GLU A 133 -77.69 -146.55
REMARK 500 9 ASP A 152 -121.18 -104.71
REMARK 500 9 LYS A 153 51.60 -155.56
REMARK 500 9 LYS A 154 -152.99 -112.48
REMARK 500 10 LYS A 2 -87.37 52.44
REMARK 500 10 SER A 89 -154.94 -103.56
REMARK 500 10 GLU A 133 -75.30 -147.13
REMARK 500 10 ASP A 152 -101.71 -108.20
REMARK 500 10 LYS A 153 43.95 -172.99
REMARK 500 10 LYS A 154 -156.55 -112.41
REMARK 500 11 THR A 3 -140.05 -90.01
REMARK 500 11 SER A 89 -153.96 -104.54
REMARK 500 11 GLU A 133 -74.61 -146.39
REMARK 500 11 ASP A 152 -108.72 -104.17
REMARK 500
REMARK 500 THIS ENTRY HAS 99 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1AMM RELATED DB: PDB
REMARK 900 RELATED ID: 1HK0 RELATED DB: PDB
REMARK 900 RELATED ID: 1A7H RELATED DB: PDB
REMARK 900 RELATED ID: 1A45 RELATED DB: PDB
REMARK 900 RELATED ID: 1A5D RELATED DB: PDB
REMARK 900 RELATED ID: 1AG4 RELATED DB: PDB
REMARK 900 RELATED ID: 1ZWO RELATED DB: PDB
DBREF 1ZWM A 1 177 UNP O35486 CRBS_MOUSE 1 177
SEQRES 1 A 177 SER LYS THR GLY GLY LYS ILE SER PHE TYR GLU ASP ARG
SEQRES 2 A 177 ASN PHE GLN GLY ARG ARG TYR ASP CYS ASP CYS ASP CYS
SEQRES 3 A 177 ALA ASP PHE ARG SER TYR LEU SER ARG CYS ASN SER ILE
SEQRES 4 A 177 ARG VAL GLU GLY GLY THR TRP ALA VAL TYR GLU ARG PRO
SEQRES 5 A 177 ASN PHE SER GLY HIS MET TYR ILE LEU PRO GLN GLY GLU
SEQRES 6 A 177 TYR PRO GLU TYR GLN ARG TRP MET GLY LEU ASN ASP ARG
SEQRES 7 A 177 LEU GLY SER CYS ARG ALA VAL HIS LEU SER SER GLY GLY
SEQRES 8 A 177 GLN ALA LYS ILE GLN VAL PHE GLU LYS GLY ASP PHE ASN
SEQRES 9 A 177 GLY GLN MET TYR GLU THR THR GLU ASP CYS PRO SER ILE
SEQRES 10 A 177 MET GLU GLN PHE HIS LEU ARG GLU ILE HIS SER CYS LYS
SEQRES 11 A 177 VAL VAL GLU GLY THR TRP ILE PHE TYR GLU LEU PRO ASN
SEQRES 12 A 177 TYR ARG GLY ARG GLN TYR LEU LEU ASP LYS LYS GLU TYR
SEQRES 13 A 177 ARG LYS PRO VAL ASP TRP GLY ALA ALA SER PRO ALA ILE
SEQRES 14 A 177 GLN SER PHE ARG ARG ILE VAL GLU
HELIX 1 1 GLU A 68 MET A 73 5 6
HELIX 2 2 SER A 116 HIS A 122 1 7
HELIX 3 3 LYS A 158 GLY A 163 5 6
SHEET 1 A 4 ARG A 19 CYS A 22 0
SHEET 2 A 4 LYS A 6 TYR A 10 -1 N ILE A 7 O CYS A 22
SHEET 3 A 4 SER A 38 GLY A 43 -1 O ARG A 40 N SER A 8
SHEET 4 A 4 GLY A 64 TYR A 66 -1 O GLY A 64 N VAL A 41
SHEET 1 B 3 SER A 55 LEU A 61 0
SHEET 2 B 3 THR A 45 ARG A 51 -1 N TRP A 46 O LEU A 61
SHEET 3 B 3 SER A 81 VAL A 85 -1 O ARG A 83 N ALA A 47
SHEET 1 C 3 ASN A 104 THR A 110 0
SHEET 2 C 3 ILE A 95 LYS A 100 -1 N VAL A 97 O TYR A 108
SHEET 3 C 3 SER A 128 VAL A 131 -1 O LYS A 130 N GLN A 96
SHEET 1 D 3 ARG A 145 LEU A 151 0
SHEET 2 D 3 TRP A 136 LEU A 141 -1 N TRP A 136 O LEU A 151
SHEET 3 D 3 SER A 171 ARG A 174 -1 O SER A 171 N TYR A 139
CRYST1 1.000 1.000 1.000 90.00 90.00 90.00 P 1 1
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 1.000000 0.000000 0.000000 0.00000
SCALE2 0.000000 1.000000 0.000000 0.00000
SCALE3 0.000000 0.000000 1.000000 0.00000
MODEL 1
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