Header list of 1wg4.pdb file
Complete list - r 2 2 Bytes
HEADER RNA BINDING PROTEIN 27-MAY-04 1WG4
TITLE SOLUTION STRUCTURE OF RRM DOMAIN IN PROTEIN BAB31986
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: HYPOTHETICAL PROTEIN (RIKEN CDNA 6030486K23);
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: RRM DOMAIN;
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: RIKEN CDNA 6030486K23;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P031208-04;
SOURCE 8 OTHER_DETAILS: CELL FREE PROTEIN SYNTHESIS
KEYWDS STRUCTURAL GENOMICS, RRM DOMAIN, RIKEN STRUCTURAL GENOMICS/PROTEOMICS
KEYWDS 2 INITIATIVE, RSGI, RNA BINDING PROTEIN
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR F.HE,Y.MUTO,M.INOUE,T.KIGAWA,M.SHIROUZU,T.TERADA,S.YOKOYAMA,RIKEN
AUTHOR 2 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE (RSGI)
REVDAT 3 02-MAR-22 1WG4 1 REMARK SEQADV
REVDAT 2 24-FEB-09 1WG4 1 VERSN
REVDAT 1 27-NOV-04 1WG4 0
JRNL AUTH F.HE,Y.MUTO,M.INOUE,T.KIGAWA,M.SHIROUZU,T.TERADA,S.YOKOYAMA
JRNL TITL SOLUTION STRUCTURE OF RRM DOMAIN IN PROTEIN BAB31986
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 1.0.8
REMARK 3 AUTHORS : BRUKER (XWINNMR), GUENTERT,P. (CYANA)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 1WG4 COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 02-JUN-04.
REMARK 100 THE DEPOSITION ID IS D_1000023543.
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 : 0.8MM U-15,13C; 20MM D-TRIS
REMARK 210 -HCL(PH 7.0); 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 : 700 MHZ
REMARK 210 SPECTROMETER MODEL : AVANCE
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NMRPIPE 20020425, NMRVIEW 5.0.4,
REMARK 210 KUJIRA 0.863, CYANA 1.0.8
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 : STRUCTURES WITH THE LEAST
REMARK 210 RESTRAINT VIOLATIONS, STRUCTURES
REMARK 210 WITH THE LOWEST ENERGY, TARGET
REMARK 210 FUNCTION
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: 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 GLU A 61 H TYR A 65 1.49
REMARK 500 O LYS A 33 H ARG A 37 1.54
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 2 -56.92 -152.73
REMARK 500 1 SER A 3 131.75 62.80
REMARK 500 1 ALA A 39 -81.95 -64.82
REMARK 500 1 LYS A 49 -171.98 -60.99
REMARK 500 1 ASP A 50 -59.68 73.46
REMARK 500 1 ASP A 71 88.61 17.96
REMARK 500 1 ASP A 72 106.88 63.96
REMARK 500 1 GLU A 81 165.24 -43.46
REMARK 500 1 SER A 92 95.26 -177.24
REMARK 500 1 SER A 93 79.63 40.34
REMARK 500 1 SER A 96 -59.62 71.74
REMARK 500 2 SER A 5 95.63 59.60
REMARK 500 2 SER A 6 85.84 61.94
REMARK 500 2 ARG A 12 33.41 -142.75
REMARK 500 2 GLN A 30 -71.62 -48.54
REMARK 500 2 ALA A 39 -80.45 -60.82
REMARK 500 2 LYS A 49 -172.91 -62.12
REMARK 500 2 ASP A 50 -58.94 74.16
REMARK 500 2 ASP A 71 90.12 18.46
REMARK 500 2 ASP A 72 106.47 60.86
REMARK 500 2 GLU A 81 139.32 -38.81
REMARK 500 2 ARG A 91 166.68 176.02
REMARK 500 2 SER A 93 126.34 64.19
REMARK 500 2 SER A 96 91.27 41.09
REMARK 500 3 SER A 2 -58.49 -126.57
REMARK 500 3 SER A 5 -57.34 -124.98
REMARK 500 3 THR A 11 98.19 -68.92
REMARK 500 3 SER A 14 153.84 -42.33
REMARK 500 3 ASP A 15 70.35 -118.13
REMARK 500 3 GLN A 30 -72.37 -48.79
REMARK 500 3 ALA A 39 -81.99 -63.88
REMARK 500 3 ASP A 50 -58.04 79.53
REMARK 500 3 ASP A 71 80.77 15.04
REMARK 500 3 ASP A 72 100.86 75.04
REMARK 500 3 SER A 93 81.58 64.98
REMARK 500 4 SER A 2 -60.49 71.33
REMARK 500 4 THR A 11 107.61 63.28
REMARK 500 4 ARG A 12 46.51 -141.59
REMARK 500 4 ASP A 15 58.30 -107.12
REMARK 500 4 GLN A 30 -73.21 -50.38
REMARK 500 4 ALA A 39 -83.15 -63.35
REMARK 500 4 ASP A 50 -57.89 75.03
REMARK 500 4 ASP A 71 86.29 15.97
REMARK 500 4 ASP A 72 104.49 68.77
REMARK 500 4 GLU A 81 156.06 -49.12
REMARK 500 4 SER A 93 155.73 -42.77
REMARK 500 4 SER A 96 78.80 66.62
REMARK 500 4 SER A 97 131.20 -179.05
REMARK 500 5 SER A 2 102.23 59.07
REMARK 500 5 SER A 6 117.59 -169.94
REMARK 500
REMARK 500 THIS ENTRY HAS 230 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 650
REMARK 650 HELIX
REMARK 650 AUTHOR DETERMINATION METHOD: AUTHOR DETERMINED
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: MMT007017169.1 RELATED DB: TARGETDB
DBREF 1WG4 A 8 92 UNP Q9D0B0 SFRS9_MOUSE 72 156
SEQADV 1WG4 GLY A 1 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 2 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 3 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 GLY A 4 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 5 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 6 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 GLY A 7 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 93 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 GLY A 94 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 PRO A 95 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 96 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 SER A 97 UNP Q9D0B0 CLONING ARTIFACT
SEQADV 1WG4 GLY A 98 UNP Q9D0B0 CLONING ARTIFACT
SEQRES 1 A 98 GLY SER SER GLY SER SER GLY GLY PRO PRO THR ARG ARG
SEQRES 2 A 98 SER ASP PHE ARG VAL LEU VAL SER GLY LEU PRO PRO SER
SEQRES 3 A 98 GLY SER TRP GLN ASP LEU LYS ASP HIS MET ARG GLU ALA
SEQRES 4 A 98 GLY ASP VAL CYS TYR ALA ASP VAL GLN LYS ASP GLY MET
SEQRES 5 A 98 GLY MET VAL GLU TYR LEU ARG LYS GLU ASP MET GLU TYR
SEQRES 6 A 98 ALA LEU ARG LYS LEU ASP ASP THR LYS PHE ARG SER HIS
SEQRES 7 A 98 GLU GLY GLU THR SER TYR ILE ARG VAL TYR PRO GLU ARG
SEQRES 8 A 98 SER SER GLY PRO SER SER GLY
HELIX 1 1 TRP A 29 MET A 36 1 8
HELIX 2 2 LYS A 60 LEU A 70 1 11
SHEET 1 A 5 VAL A 42 GLN A 48 0
SHEET 2 A 5 MET A 52 TYR A 57 -1 O MET A 54 N ASP A 46
SHEET 3 A 5 ARG A 17 SER A 21 -1 N VAL A 20 O GLY A 53
SHEET 4 A 5 THR A 82 TYR A 88 -1 O TYR A 88 N LEU A 19
SHEET 5 A 5 THR A 73 ARG A 76 -1 N PHE A 75 O SER A 83
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