Header list of 2ctu.pdb file
Complete list - r 9 2 Bytes
HEADER TRANSCRIPTION 24-MAY-05 2CTU
TITLE SOLUTION STRUCTURE OF ZINC FINGER DOMAIN FROM HUMAN ZN FINGER PROTEIN
TITLE 2 483
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: ZINC FINGER PROTEIN 483;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: ZINC FINGER DOMAIN;
COMPND 5 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: HOMO SAPIENS;
SOURCE 3 ORGANISM_COMMON: HUMAN;
SOURCE 4 ORGANISM_TAXID: 9606;
SOURCE 5 GENE: ZNF483;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P040910-15;
SOURCE 8 OTHER_DETAILS: CELL FREE PROTEIN SYNTHESIS
KEYWDS ZINC FINGER DOMAIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON
KEYWDS 2 PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL
KEYWDS 3 GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSCRIPTION
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR N.KOBAYASHI,T.TOMIZAWA,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA,RIKEN
AUTHOR 2 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE (RSGI)
REVDAT 3 09-MAR-22 2CTU 1 REMARK SEQADV LINK
REVDAT 2 24-FEB-09 2CTU 1 VERSN
REVDAT 1 24-NOV-05 2CTU 0
JRNL AUTH N.KOBAYASHI,T.TOMIZAWA,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA
JRNL TITL SOLUTION STRUCTURE OF ZINC FINGER DOMAIN FROM HUMAN ZN
JRNL TITL 2 FINGER PROTEIN 483
JRNL REF TO BE PUBLISHED
JRNL REFN
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : XWINNMR 2.6, CYANA 2.0.17
REMARK 3 AUTHORS : BRUKER (XWINNMR), GUNTERT, P. (CYANA)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 2CTU COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 01-JUN-05.
REMARK 100 THE DEPOSITION ID IS D_1000024612.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 298
REMARK 210 PH : 7.0
REMARK 210 IONIC STRENGTH : 120MM
REMARK 210 PRESSURE : AMBIENT
REMARK 210 SAMPLE CONTENTS : 1.29MM ZN-FINGER DOMAIN U
REMARK 210 -13C,15N; 20MM PHOSPHATE BUFFER
REMARK 210 NA (PH7.0); 100MM NACL; 1MM D-
REMARK 210 DTT; 0.02% NAN3; 0.05MM ZNCL2;
REMARK 210 10% D2O
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_15N-SEPARATED_NOESY; 3D_13C
REMARK 210 -SEPARATED_NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 800 MHZ
REMARK 210 SPECTROMETER MODEL : AVANCE
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NMRPIPE 20031121, NMRVIEW 5.0.4,
REMARK 210 KUJIRA 0.9297, CYANA 2.0.17
REMARK 210 METHOD USED : TOSION ANGLE DYNAMICS
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 100
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 20
REMARK 210 CONFORMERS, SELECTION CRITERIA : TARGET FUNCTION,STRUCTURES WITH
REMARK 210 THE LOWEST ENERGY,STRUCTURES
REMARK 210 WITH THE LEAST RESTRAINT
REMARK 210 VIOLATIONS
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 1
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: 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 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 ARG A 9 97.07 -60.96
REMARK 500 1 ARG A 17 -39.54 -34.61
REMARK 500 1 SER A 18 123.55 -39.69
REMARK 500 1 LEU A 34 99.85 -66.93
REMARK 500 1 SER A 35 114.05 -36.25
REMARK 500 1 ARG A 36 -51.68 -123.43
REMARK 500 1 LYS A 38 56.10 -90.39
REMARK 500 1 ASP A 48 49.71 -84.28
REMARK 500 1 GLU A 52 98.55 -62.27
REMARK 500 1 LYS A 57 -59.32 -125.85
REMARK 500 2 ARG A 17 42.63 -85.00
REMARK 500 2 CYS A 21 161.14 -43.30
REMARK 500 2 ARG A 36 132.42 -37.97
REMARK 500 2 PRO A 40 91.88 -69.81
REMARK 500 2 LYS A 47 37.96 -95.12
REMARK 500 2 SER A 49 77.86 -110.59
REMARK 500 2 ALA A 53 115.90 -165.68
REMARK 500 2 ALA A 54 79.92 -115.71
REMARK 500 2 THR A 67 91.81 -47.99
REMARK 500 2 PRO A 70 85.55 -69.73
REMARK 500 2 SER A 72 140.34 -36.06
REMARK 500 3 LYS A 8 145.27 -170.46
REMARK 500 3 LYS A 11 157.39 -39.55
REMARK 500 3 HIS A 13 44.32 -86.06
REMARK 500 3 CYS A 21 158.33 -44.87
REMARK 500 3 SER A 32 168.87 -49.06
REMARK 500 3 PRO A 40 88.77 -69.74
REMARK 500 3 ASP A 48 40.14 -83.96
REMARK 500 3 SER A 49 41.08 -104.96
REMARK 500 3 ALA A 53 40.93 34.65
REMARK 500 3 ASN A 61 -44.19 -131.37
REMARK 500 4 ARG A 31 -62.77 -107.00
REMARK 500 4 LEU A 55 149.26 -36.82
REMARK 500 4 ASN A 56 -62.23 -91.79
REMARK 500 4 GLU A 62 71.07 -109.88
REMARK 500 4 SER A 71 112.45 -35.75
REMARK 500 5 ASP A 16 -43.68 -131.20
REMARK 500 5 PRO A 40 81.56 -69.74
REMARK 500 5 ASP A 48 35.25 -83.55
REMARK 500 5 SER A 49 40.53 33.57
REMARK 500 5 GLN A 51 178.31 -51.27
REMARK 500 5 LEU A 55 150.16 -35.37
REMARK 500 5 LYS A 57 126.04 -31.76
REMARK 500 5 ASP A 58 -59.12 -122.28
REMARK 500 5 ASN A 61 -56.75 -122.28
REMARK 500 5 GLU A 62 -60.77 -124.65
REMARK 500 5 LYS A 65 156.66 -42.86
REMARK 500 5 SER A 68 40.23 34.82
REMARK 500 5 PRO A 70 3.47 -69.73
REMARK 500 6 SER A 18 121.45 -38.50
REMARK 500
REMARK 500 THIS ENTRY HAS 201 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
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 ZN A 201 ZN
REMARK 620 N RES CSSEQI ATOM
REMARK 620 1 CYS A 21 SG
REMARK 620 2 CYS A 24 SG 111.5
REMARK 620 3 CYS A 42 SG 117.9 93.7
REMARK 620 4 CYS A 45 SG 113.5 113.5 105.2
REMARK 620 N 1 2 3
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: AC1
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE ZN A 201
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: HSK002001929.1 RELATED DB: TARGETDB
DBREF 2CTU A 8 67 UNP Q8TF39 ZN483_HUMAN 379 438
SEQADV 2CTU GLY A 1 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 2 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 3 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU GLY A 4 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 5 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 6 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU GLY A 7 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 68 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU GLY A 69 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU PRO A 70 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 71 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU SER A 72 UNP Q8TF39 CLONING ARTIFACT
SEQADV 2CTU GLY A 73 UNP Q8TF39 CLONING ARTIFACT
SEQRES 1 A 73 GLY SER SER GLY SER SER GLY LYS ARG GLN LYS ILE HIS
SEQRES 2 A 73 LEU GLY ASP ARG SER GLN LYS CYS SER LYS CYS GLY ILE
SEQRES 3 A 73 ILE PHE ILE ARG ARG SER THR LEU SER ARG ARG LYS THR
SEQRES 4 A 73 PRO MET CYS GLU LYS CYS ARG LYS ASP SER CYS GLN GLU
SEQRES 5 A 73 ALA ALA LEU ASN LYS ASP GLU GLY ASN GLU SER GLY LYS
SEQRES 6 A 73 LYS THR SER GLY PRO SER SER GLY
HET ZN A 201 1
HETNAM ZN ZINC ION
FORMUL 2 ZN ZN 2+
HELIX 1 1 CYS A 42 ASP A 48 1 7
SHEET 1 A 2 SER A 18 LYS A 20 0
SHEET 2 A 2 ILE A 27 ILE A 29 -1 O PHE A 28 N GLN A 19
LINK SG CYS A 21 ZN ZN A 201 1555 1555 2.34
LINK SG CYS A 24 ZN ZN A 201 1555 1555 2.33
LINK SG CYS A 42 ZN ZN A 201 1555 1555 2.33
LINK SG CYS A 45 ZN ZN A 201 1555 1555 2.33
SITE 1 AC1 4 CYS A 21 CYS A 24 CYS A 42 CYS A 45
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 9 2 Bytes