Header list of 2ezp.pdb file
Complete list - r 25 2 Bytes
HEADER VIRAL PROTEIN 20-MAY-98 2EZP
TITLE SOLUTION NMR STRUCTURE OF ECTODOMAIN OF SIV GP41, MODELS 1-10 OF AN
TITLE 2 ENSEMBLE OF 40 SIMULATED ANNEALING STRUCTURES
SPLIT 2EZP 2EZQ 2EZR 2EZS
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: GP41;
COMPND 3 CHAIN: A, B, C;
COMPND 4 FRAGMENT: ECTODOMAIN, RESIDUES 27 - 149, NUMBERED 1 - 123
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: SIMIAN IMMUNODEFICIENCY VIRUS;
SOURCE 3 ORGANISM_TAXID: 11723;
SOURCE 4 STRAIN: SOOTEY MANGABEY
KEYWDS VIRUS ENVELOPE PROTEIN, SIV GP41 ECTODOMAIN, VIRAL PROTEIN
EXPDTA SOLUTION NMR
NUMMDL 10
AUTHOR M.CAFFREY,A.M.GRONENBORN,G.M.CLORE
REVDAT 3 24-NOV-10 2EZP 1 REMARK
REVDAT 2 24-FEB-09 2EZP 1 VERSN
REVDAT 1 14-OCT-98 2EZP 0
JRNL AUTH M.CAFFREY,M.CAI,J.KAUFMAN,S.J.STAHL,P.T.WINGFIELD,
JRNL AUTH 2 D.G.COVELL,A.M.GRONENBORN,G.M.CLORE
JRNL TITL THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE 44 KDA
JRNL TITL 2 ECTODOMAIN OF SIV GP41.
JRNL REF EMBO J. V. 17 4572 1998
JRNL REFN ISSN 0261-4189
JRNL PMID 9707417
JRNL DOI 10.1093/EMBOJ/17.16.4572
REMARK 1
REMARK 1 REFERENCE 1
REMARK 1 AUTH M.CAFFREY,M.CAI,J.KAUFMAN,S.J.STAHL,P.T.WINGFIELD,
REMARK 1 AUTH 2 A.M.GRONENBORN,G.M.CLORE
REMARK 1 TITL DETERMINATION OF THE SECONDARY STRUCTURE AND GLOBAL TOPOLOGY
REMARK 1 TITL 2 OF THE 44 KDA ECTODOMAIN OF GP41 OF THE SIMIAN
REMARK 1 TITL 3 IMMUNODEFICIENCY VIRUS BY MULTIDIMENSIONAL NUCLEAR MAGNETIC
REMARK 1 TITL 4 RESONANCE SPECTROSCOPY
REMARK 1 REF J.MOL.BIOL. V. 271 819 1997
REMARK 1 REFN ISSN 0022-2836
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : CNS
REMARK 3 AUTHORS : BRUNGER,ADAMS,CLORE,DELANO,GROS,GROSSE-KUNSTLEVE,
REMARK 3 JIANG,KUSZEWSKI,NILGES,PANNU,READ,RICE,SIMONSON,WARREN
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NO REFINEMENT WAS DONE
REMARK 4
REMARK 4 2EZP COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY BNL.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 322
REMARK 210 PH : 3.0
REMARK 210 IONIC STRENGTH : NULL
REMARK 210 PRESSURE : NULL
REMARK 210 SAMPLE CONTENTS : NULL
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : TRIPLE RESONANCE FOR ASSIGNMENT
REMARK 210 OF PROTEIN: D-HNCA; D-HNCO; D-
REMARK 210 HN(CO)CA; D-HN(CA)CO D-HNCACB; D-
REMARK 210 HN(COCA)CB; D-HN(CA)CB; D-C(CC)
REMARK 210 (CO)NH; HBHA(CO)NH; HCACO; HNHA;
REMARK 210 HCCH-COSY; HCCH-TOCSY; 4D HCCH
REMARK 210 13C-13C NOE; QUANTITATIVE J
REMARK 210 CORRELATION FOR COUPLING
REMARK 210 CONSTANTS; 3D 15N-SEPARATED NOE
REMARK 210 AND ROE; 3D 13C-SEPARATED NOE; 3D
REMARK 210 13C-SEPARATED/12C_FILTERED NOE;
REMARK 210 3D 13C-SEPARATED/15N-FILTERED
REMARK 210 NOE; 3D 15N-SEPARATED/13C-
REMARK 210 FILTERED NOE; 4D 15N/15N-
REMARK 210 SEPARATED NOE; 4D 15N/13C-
REMARK 210 SEPARATED NOE; 4D 13C/13C-
REMARK 210 SEPARATED NOE EXPERIMENTS: 3D
REMARK 210 HCA(CO)N FOR THREE-BOND AMIDE
REMARK 210 DEUTERIUM ISOTOPE SHIFTS;
REMARK 210 SPECTROMETER FIELD STRENGTH : 500 MHZ; 600 MHZ; 750 MHZ
REMARK 210 SPECTROMETER MODEL : DMX500; DMX600; DMX750
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : CNS
REMARK 210 METHOD USED : SIMULATED ANNEALING
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 40
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 10
REMARK 210 CONFORMERS, SELECTION CRITERIA : NULL
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : NULL
REMARK 210
REMARK 210 REMARK: NULL
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: TRIMERIC
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A, B, C
REMARK 350 BIOMT1 1 1.000000 0.000000 0.000000 0.00000
REMARK 350 BIOMT2 1 0.000000 1.000000 0.000000 0.00000
REMARK 350 BIOMT3 1 0.000000 0.000000 1.000000 0.00000
REMARK 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 O ASN B 37 HG1 THR B 40 1.51
REMARK 500 O ASN C 37 HG1 THR C 40 1.52
REMARK 500 O ASN A 37 HG1 THR A 40 1.52
REMARK 500 O LEU B 28 HG1 THR B 31 1.59
REMARK 500 O LEU C 28 HG1 THR C 31 1.59
REMARK 500 O LEU A 28 HG1 THR A 31 1.60
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 ASN A 56 -64.16 -132.80
REMARK 500 1 ALA A 60 23.60 -75.45
REMARK 500 1 VAL A 65 58.10 -100.87
REMARK 500 1 PRO A 73 149.76 -38.27
REMARK 500 1 ASN A 74 -57.13 -129.05
REMARK 500 1 ASN B 56 -63.96 -132.74
REMARK 500 1 ALA B 60 23.70 -75.47
REMARK 500 1 VAL B 65 58.15 -100.89
REMARK 500 1 PRO B 73 149.86 -38.26
REMARK 500 1 ASN B 74 -56.99 -129.26
REMARK 500 1 ASN C 56 -64.03 -132.85
REMARK 500 1 ALA C 60 23.56 -75.38
REMARK 500 1 VAL C 65 58.09 -100.85
REMARK 500 1 PRO C 73 149.75 -38.26
REMARK 500 1 ASN C 74 -57.04 -129.13
REMARK 500 2 ASN A 56 -63.18 -133.44
REMARK 500 2 ALA A 60 24.02 -77.12
REMARK 500 2 VAL A 65 60.26 -107.49
REMARK 500 2 PRO A 73 148.08 -38.31
REMARK 500 2 ASN A 74 -56.16 -124.80
REMARK 500 2 ASN B 56 -62.87 -133.58
REMARK 500 2 ALA B 60 23.77 -77.16
REMARK 500 2 VAL B 65 60.19 -107.65
REMARK 500 2 PRO B 73 148.14 -38.31
REMARK 500 2 ASN B 74 -56.43 -124.88
REMARK 500 2 ASN C 56 -62.71 -133.64
REMARK 500 2 ALA C 60 24.03 -77.61
REMARK 500 2 VAL C 65 60.23 -107.54
REMARK 500 2 PRO C 73 148.25 -38.35
REMARK 500 2 ASN C 74 -56.84 -124.97
REMARK 500 3 SER A 3 59.87 -91.20
REMARK 500 3 ASN A 56 -72.12 -133.15
REMARK 500 3 ALA A 60 24.84 -73.89
REMARK 500 3 VAL A 65 58.66 -107.10
REMARK 500 3 PRO A 73 147.63 -38.32
REMARK 500 3 ASN A 74 -58.76 -130.70
REMARK 500 3 ASN A 122 58.86 -116.48
REMARK 500 3 SER B 3 59.89 -90.88
REMARK 500 3 ASN B 56 -72.28 -133.24
REMARK 500 3 ALA B 60 25.14 -74.32
REMARK 500 3 VAL B 65 58.47 -107.06
REMARK 500 3 PRO B 73 147.66 -38.18
REMARK 500 3 ASN B 74 -59.50 -130.52
REMARK 500 3 ASN B 122 58.60 -116.38
REMARK 500 3 SER C 3 59.85 -91.07
REMARK 500 3 ASN C 56 -72.25 -133.23
REMARK 500 3 ALA C 60 24.92 -73.69
REMARK 500 3 VAL C 65 58.49 -107.20
REMARK 500 3 PRO C 73 147.59 -38.32
REMARK 500 3 ASN C 74 -59.26 -130.49
REMARK 500
REMARK 500 THIS ENTRY HAS 184 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 2EZO RELATED DB: PDB
REMARK 900 RELATED ID: 2EZQ RELATED DB: PDB
REMARK 900 RELATED ID: 2EZR RELATED DB: PDB
REMARK 900 RELATED ID: 2EZS RELATED DB: PDB
DBREF 2EZP A 1 123 UNP Q88028 Q88028_SIVCZ 150 272
DBREF 2EZP B 1 123 UNP Q88028 Q88028_SIVCZ 150 272
DBREF 2EZP C 1 123 UNP Q88028 Q88028_SIVCZ 150 272
SEQADV 2EZP ALA A 60 UNP Q88028 CYS 209 CONFLICT
SEQADV 2EZP ALA A 66 UNP Q88028 CYS 215 CONFLICT
SEQADV 2EZP LYS A 80 UNP Q88028 ASP 229 CONFLICT
SEQADV 2EZP GLU A 84 UNP Q88028 ASP 233 CONFLICT
SEQADV 2EZP ALA B 60 UNP Q88028 CYS 209 CONFLICT
SEQADV 2EZP ALA B 66 UNP Q88028 CYS 215 CONFLICT
SEQADV 2EZP LYS B 80 UNP Q88028 ASP 229 CONFLICT
SEQADV 2EZP GLU B 84 UNP Q88028 ASP 233 CONFLICT
SEQADV 2EZP ALA C 60 UNP Q88028 CYS 209 CONFLICT
SEQADV 2EZP ALA C 66 UNP Q88028 CYS 215 CONFLICT
SEQADV 2EZP LYS C 80 UNP Q88028 ASP 229 CONFLICT
SEQADV 2EZP GLU C 84 UNP Q88028 ASP 233 CONFLICT
SEQRES 1 A 123 ALA GLN SER ARG THR LEU LEU ALA GLY ILE VAL GLN GLN
SEQRES 2 A 123 GLN GLN GLN LEU LEU ASP VAL VAL LYS ARG GLN GLN GLU
SEQRES 3 A 123 LEU LEU ARG LEU THR VAL TRP GLY THR LYS ASN LEU GLN
SEQRES 4 A 123 THR ARG VAL THR ALA ILE GLU LYS TYR LEU LYS ASP GLN
SEQRES 5 A 123 ALA GLN LEU ASN ALA TRP GLY ALA ALA PHE ARG GLN VAL
SEQRES 6 A 123 ALA HIS THR THR VAL PRO TRP PRO ASN ALA SER LEU THR
SEQRES 7 A 123 PRO LYS TRP ASN ASN GLU THR TRP GLN GLU TRP GLU ARG
SEQRES 8 A 123 LYS VAL ASP PHE LEU GLU GLU ASN ILE THR ALA LEU LEU
SEQRES 9 A 123 GLU GLU ALA GLN ILE GLN GLN GLU LYS ASN MET TYR GLU
SEQRES 10 A 123 LEU GLN LYS LEU ASN SER
SEQRES 1 B 123 ALA GLN SER ARG THR LEU LEU ALA GLY ILE VAL GLN GLN
SEQRES 2 B 123 GLN GLN GLN LEU LEU ASP VAL VAL LYS ARG GLN GLN GLU
SEQRES 3 B 123 LEU LEU ARG LEU THR VAL TRP GLY THR LYS ASN LEU GLN
SEQRES 4 B 123 THR ARG VAL THR ALA ILE GLU LYS TYR LEU LYS ASP GLN
SEQRES 5 B 123 ALA GLN LEU ASN ALA TRP GLY ALA ALA PHE ARG GLN VAL
SEQRES 6 B 123 ALA HIS THR THR VAL PRO TRP PRO ASN ALA SER LEU THR
SEQRES 7 B 123 PRO LYS TRP ASN ASN GLU THR TRP GLN GLU TRP GLU ARG
SEQRES 8 B 123 LYS VAL ASP PHE LEU GLU GLU ASN ILE THR ALA LEU LEU
SEQRES 9 B 123 GLU GLU ALA GLN ILE GLN GLN GLU LYS ASN MET TYR GLU
SEQRES 10 B 123 LEU GLN LYS LEU ASN SER
SEQRES 1 C 123 ALA GLN SER ARG THR LEU LEU ALA GLY ILE VAL GLN GLN
SEQRES 2 C 123 GLN GLN GLN LEU LEU ASP VAL VAL LYS ARG GLN GLN GLU
SEQRES 3 C 123 LEU LEU ARG LEU THR VAL TRP GLY THR LYS ASN LEU GLN
SEQRES 4 C 123 THR ARG VAL THR ALA ILE GLU LYS TYR LEU LYS ASP GLN
SEQRES 5 C 123 ALA GLN LEU ASN ALA TRP GLY ALA ALA PHE ARG GLN VAL
SEQRES 6 C 123 ALA HIS THR THR VAL PRO TRP PRO ASN ALA SER LEU THR
SEQRES 7 C 123 PRO LYS TRP ASN ASN GLU THR TRP GLN GLU TRP GLU ARG
SEQRES 8 C 123 LYS VAL ASP PHE LEU GLU GLU ASN ILE THR ALA LEU LEU
SEQRES 9 C 123 GLU GLU ALA GLN ILE GLN GLN GLU LYS ASN MET TYR GLU
SEQRES 10 C 123 LEU GLN LYS LEU ASN SER
HELIX 1 1 ARG A 4 GLN A 54 1 51
HELIX 2 2 TRP A 81 LEU A 121 1 41
HELIX 3 3 ARG B 4 GLN B 54 1 51
HELIX 4 4 TRP B 81 LEU B 121 1 41
HELIX 5 5 ARG C 4 GLN C 54 1 51
HELIX 6 6 TRP C 81 LEU C 121 1 41
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
Complete list - r 25 2 Bytes