Header list of 2d8j.pdb file
Complete list - r 9 2 Bytes
HEADER TRANSFERASE 06-DEC-05 2D8J
TITLE SOLUTION STRUCTURE OF THE SH3 DOMAIN OF FYN-RELATED KINASE
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: FYN-RELATED KINASE;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: SH3 DOMAIN;
COMPND 5 EC: 2.7.1.112;
COMPND 6 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: FRK;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P050425-22;
SOURCE 8 OTHER_DETAILS: CELL FREE PROTEIN SYNTHESIS
KEYWDS SH3 DOMAIN, FYN-RELATED KINASE, STRUCTURAL GENOMICS, NPPSFA, NATIONAL
KEYWDS 2 PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN
KEYWDS 3 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR X.R.QIN,C.KUROSAKI,M.YOSHIDA,F.HAYASHI,S.YOKOYAMA,RIKEN STRUCTURAL
AUTHOR 2 GENOMICS/PROTEOMICS INITIATIVE (RSGI)
REVDAT 3 09-MAR-22 2D8J 1 REMARK SEQADV
REVDAT 2 24-FEB-09 2D8J 1 VERSN
REVDAT 1 06-JUN-06 2D8J 0
JRNL AUTH X.R.QIN,C.KUROSAKI,M.YOSHIDA,F.HAYASHI,S.YOKOYAMA
JRNL TITL SOLUTION STRUCTURE OF THE SH3 DOMAIN OF FYN-RELATED KINASE
JRNL REF TO BE PUBLISHED
JRNL REFN
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : DELTA NMR 4.3, CYANA 2.0.17
REMARK 3 AUTHORS : JEOL (DELTA NMR), GUNTERT, P. (CYANA)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 2D8J COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 09-DEC-05.
REMARK 100 THE DEPOSITION ID IS D_1000025120.
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 : 1.17MM 13C,15N-LABELED PROTEIN;
REMARK 210 20MM D-TRIS-HCL(PH7.0); 100MM
REMARK 210 NACL; 1MM D-DTT; 0.02% NAN3
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 : ECA
REMARK 210 SPECTROMETER MANUFACTURER : JEOL
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NMRPIPE 20031121, NMRVIEW 5.0.4,
REMARK 210 KUJIRA 0.9296, CYANA 2.0.17
REMARK 210 METHOD USED : TORSION 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 SER A 6 171.85 -58.19
REMARK 500 1 SER A 38 45.94 -88.16
REMARK 500 1 HIS A 39 119.33 -174.05
REMARK 500 1 LYS A 50 152.57 -45.91
REMARK 500 1 LYS A 51 134.46 -35.00
REMARK 500 2 SER A 2 -55.73 -120.77
REMARK 500 2 ALA A 21 35.38 -90.03
REMARK 500 2 LYS A 51 -54.54 -123.28
REMARK 500 2 GLN A 57 37.55 -91.04
REMARK 500 2 PRO A 74 82.84 -69.72
REMARK 500 3 ALA A 28 108.90 -59.71
REMARK 500 3 HIS A 39 83.82 -59.76
REMARK 500 3 GLU A 40 134.11 -36.93
REMARK 500 3 PRO A 74 95.54 -69.81
REMARK 500 4 ASP A 30 109.89 -41.45
REMARK 500 4 GLU A 40 50.52 -92.11
REMARK 500 4 LYS A 50 141.91 -172.01
REMARK 500 4 LEU A 55 138.04 -37.92
REMARK 500 4 LEU A 59 -19.72 -48.97
REMARK 500 4 PRO A 74 2.69 -69.80
REMARK 500 5 ASP A 30 136.27 -38.26
REMARK 500 5 GLU A 40 98.63 -69.40
REMARK 500 5 LEU A 55 -62.50 -121.37
REMARK 500 5 GLN A 58 173.82 -49.71
REMARK 500 5 PRO A 74 93.09 -69.71
REMARK 500 5 SER A 76 104.52 -43.50
REMARK 500 6 SER A 3 108.73 -55.45
REMARK 500 6 ALA A 18 105.68 -53.77
REMARK 500 6 ASP A 30 110.72 -35.29
REMARK 500 6 HIS A 39 89.21 -66.41
REMARK 500 6 LYS A 51 -62.26 -102.55
REMARK 500 7 ALA A 18 144.12 -38.49
REMARK 500 7 SER A 38 44.12 -89.90
REMARK 500 7 HIS A 39 111.80 -171.85
REMARK 500 7 GLU A 40 75.61 -68.32
REMARK 500 7 THR A 53 40.68 -91.95
REMARK 500 7 SER A 75 85.38 -67.78
REMARK 500 8 GLU A 22 56.38 -97.23
REMARK 500 8 SER A 38 -73.72 -86.89
REMARK 500 8 HIS A 39 98.83 -50.41
REMARK 500 8 SER A 72 85.43 -53.01
REMARK 500 9 ASP A 30 136.45 -39.33
REMARK 500 9 SER A 38 -74.71 -80.96
REMARK 500 9 HIS A 39 97.36 -55.21
REMARK 500 9 GLN A 58 174.00 -59.31
REMARK 500 9 SER A 72 102.74 -54.52
REMARK 500 10 ALA A 28 107.50 -53.70
REMARK 500 10 GLU A 49 102.76 -53.23
REMARK 500 11 SER A 5 41.67 -95.10
REMARK 500 11 SER A 38 -73.92 -80.33
REMARK 500
REMARK 500 THIS ENTRY HAS 96 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: MMT008000775.2 RELATED DB: TARGETDB
DBREF 2D8J A 8 71 GB 31542823 NP_034367 52 115
SEQADV 2D8J GLY A 1 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 2 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 3 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J GLY A 4 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 5 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 6 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J GLY A 7 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 72 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J GLY A 73 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J PRO A 74 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 75 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J SER A 76 GB 31542823 CLONING ARTIFACT
SEQADV 2D8J GLY A 77 GB 31542823 CLONING ARTIFACT
SEQRES 1 A 77 GLY SER SER GLY SER SER GLY GLN TYR PHE VAL ALA LEU
SEQRES 2 A 77 PHE ASP TYR GLN ALA ARG THR ALA GLU ASP LEU SER PHE
SEQRES 3 A 77 ARG ALA GLY ASP LYS LEU GLN VAL LEU ASP THR SER HIS
SEQRES 4 A 77 GLU GLY TRP TRP LEU ALA ARG HIS LEU GLU LYS LYS GLY
SEQRES 5 A 77 THR GLY LEU GLY GLN GLN LEU GLN GLY TYR ILE PRO SER
SEQRES 6 A 77 ASN TYR VAL ALA GLU ASP SER GLY PRO SER SER GLY
SHEET 1 A 5 GLN A 60 PRO A 64 0
SHEET 2 A 5 TRP A 42 HIS A 47 -1 N TRP A 43 O ILE A 63
SHEET 3 A 5 LEU A 32 ASP A 36 -1 N LEU A 35 O LEU A 44
SHEET 4 A 5 GLN A 8 ALA A 12 -1 N PHE A 10 O LEU A 32
SHEET 5 A 5 VAL A 68 GLU A 70 -1 O ALA A 69 N VAL A 11
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