Header list of 1wx6.pdb file
Complete list - r 2 2 Bytes
HEADER STRUCTURAL GENOMICS, UNKNOWN FUNCTION 20-JAN-05 1WX6
TITLE SOLUTION STRUCTURE OF THE SH3 DOMAIN OF THE HUMAN CYTOPLASMIC PROTEIN
TITLE 2 NCK2
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: CYTOPLASMIC PROTEIN NCK2;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: SH3 DOMAIN;
COMPND 5 SYNONYM: NCK ADAPTOR PROTEIN 2, SH2/SH3 ADAPTOR PROTEIN NCK-BETA,
COMPND 6 NCK-2;
COMPND 7 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: NCK2;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P040802-08;
SOURCE 8 OTHER_DETAILS: CELL-FREE PROTEIN SYNTHESIS
KEYWDS SH3 DOMAIN, NCK2, STRUCTURAL GENOMICS, SIGNAL TRANSDUCTION, RIKEN
KEYWDS 2 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, UNKNOWN FUNCTION
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR S.OHNISHI,T.KIGAWA,T.TOMIZAWA,S.KOSHIBA,M.INOUE,S.YOKOYAMA,RIKEN
AUTHOR 2 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE (RSGI)
REVDAT 3 02-MAR-22 1WX6 1 REMARK SEQADV
REVDAT 2 24-FEB-09 1WX6 1 VERSN
REVDAT 1 20-JUL-05 1WX6 0
JRNL AUTH S.OHNISHI,T.KIGAWA,T.TOMIZAWA,S.KOSHIBA,M.INOUE,S.YOKOYAMA
JRNL TITL SOLUTION STRUCTURE OF THE SH3 DOMAIN OF THE HUMAN
JRNL TITL 2 CYTOPLASMIC PROTEIN NCK2
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), GUENTERT, P. (CYANA)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: THE STRUCTURES WERE CALCULATED USING
REMARK 3 3296 NOE-DERIVED DISTANCE CONSTRAINTS.
REMARK 4
REMARK 4 1WX6 COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 21-JAN-05.
REMARK 100 THE DEPOSITION ID IS D_1000024106.
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 : 1.28MM PROTEIN U-15N, 13C; 20MM
REMARK 210 D-TRIS-HCL; 100MM NACL; 1MM D-
REMARK 210 DTT; 0.02% NAN3; 90% H2O, 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 20030801, NMRVIEW 5.0.4,
REMARK 210 KUJIRA 0.914, CYANA 2.0.17
REMARK 210 METHOD USED : TORSION ANGLE DYNAMICS,
REMARK 210 RESTRAINED MOLECULAR 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 LEAST RESTRAINT 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 LEU A 75 -60.19 -93.12
REMARK 500 1 PRO A 79 87.52 -69.68
REMARK 500 1 PRO A 83 99.28 -69.80
REMARK 500 1 PRO A 88 2.76 -69.80
REMARK 500 1 SER A 89 131.66 -36.22
REMARK 500 2 GLU A 31 32.55 -87.92
REMARK 500 2 PRO A 48 98.12 -69.78
REMARK 500 2 HIS A 82 54.21 34.51
REMARK 500 2 PRO A 83 -173.81 -69.75
REMARK 500 3 GLN A 12 166.50 -45.62
REMARK 500 3 GLU A 49 -50.66 -120.83
REMARK 500 3 LEU A 75 -60.28 -100.54
REMARK 500 3 ASP A 77 74.94 -118.47
REMARK 500 3 PRO A 79 0.49 -69.75
REMARK 500 3 ALA A 80 77.05 -61.00
REMARK 500 3 PRO A 88 2.78 -69.78
REMARK 500 4 PRO A 79 2.78 -69.78
REMARK 500 4 ALA A 80 40.70 72.42
REMARK 500 4 SER A 90 42.58 39.07
REMARK 500 5 SER A 2 84.39 -68.22
REMARK 500 5 SER A 5 42.37 70.53
REMARK 500 5 ASN A 10 173.53 -48.26
REMARK 500 5 SER A 14 119.12 -163.18
REMARK 500 5 PRO A 79 1.83 -69.74
REMARK 500 5 HIS A 82 140.70 -36.20
REMARK 500 5 ALA A 84 149.37 -38.86
REMARK 500 6 LEU A 8 42.86 -101.00
REMARK 500 6 PRO A 79 97.43 -69.79
REMARK 500 6 ALA A 80 98.24 -41.05
REMARK 500 6 LEU A 81 41.96 34.31
REMARK 500 6 HIS A 85 -53.07 -124.01
REMARK 500 7 SER A 3 96.76 -62.45
REMARK 500 7 GLN A 12 156.51 -38.72
REMARK 500 7 SER A 14 165.48 -46.70
REMARK 500 7 LEU A 75 -60.16 -92.34
REMARK 500 7 ALA A 80 47.16 74.10
REMARK 500 8 SER A 2 -54.62 -124.64
REMARK 500 8 SER A 3 89.61 -67.58
REMARK 500 8 LEU A 8 -46.46 -131.29
REMARK 500 8 SER A 14 89.33 -62.83
REMARK 500 8 LEU A 17 -60.39 -94.51
REMARK 500 8 ALA A 80 97.66 -67.21
REMARK 500 8 ALA A 84 161.63 -43.45
REMARK 500 9 GLN A 12 -58.03 -123.72
REMARK 500 9 ASP A 77 75.48 -106.92
REMARK 500 9 ALA A 80 99.65 -34.12
REMARK 500 9 SER A 90 -53.18 -126.13
REMARK 500 10 ASN A 10 89.01 -61.36
REMARK 500 10 SER A 14 126.00 -36.69
REMARK 500 10 ALA A 80 50.77 73.97
REMARK 500
REMARK 500 THIS ENTRY HAS 90 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: HSI002004659.1 RELATED DB: TARGETDB
DBREF 1WX6 A 8 85 UNP O43639 NCK2_HUMAN 188 265
SEQADV 1WX6 GLY A 1 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 2 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 3 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 GLY A 4 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 5 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 6 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 GLY A 7 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 86 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 GLY A 87 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 PRO A 88 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 89 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 SER A 90 UNP O43639 CLONING ARTIFACT
SEQADV 1WX6 GLY A 91 UNP O43639 CLONING ARTIFACT
SEQRES 1 A 91 GLY SER SER GLY SER SER GLY LEU SER ASN GLY GLN GLY
SEQRES 2 A 91 SER ARG VAL LEU HIS VAL VAL GLN THR LEU TYR PRO PHE
SEQRES 3 A 91 SER SER VAL THR GLU GLU GLU LEU ASN PHE GLU LYS GLY
SEQRES 4 A 91 GLU THR MET GLU VAL ILE GLU LYS PRO GLU ASN ASP PRO
SEQRES 5 A 91 GLU TRP TRP LYS CYS LYS ASN ALA ARG GLY GLN VAL GLY
SEQRES 6 A 91 LEU VAL PRO LYS ASN TYR VAL VAL VAL LEU SER ASP GLY
SEQRES 7 A 91 PRO ALA LEU HIS PRO ALA HIS SER GLY PRO SER SER GLY
SHEET 1 A 5 VAL A 64 PRO A 68 0
SHEET 2 A 5 TRP A 54 LYS A 58 -1 N TRP A 55 O VAL A 67
SHEET 3 A 5 THR A 41 GLU A 46 -1 N GLU A 46 O LYS A 56
SHEET 4 A 5 HIS A 18 THR A 22 -1 N VAL A 20 O MET A 42
SHEET 5 A 5 VAL A 72 ASP A 77 -1 O LEU A 75 N VAL A 19
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 2 2 Bytes