Header list of 1wex.pdb file
Complete list - r 2 2 Bytes
HEADER RNA BINDING PROTEIN 25-MAY-04 1WEX
TITLE SOLUTION STRUCTURE OF RRM DOMAIN IN PROTEIN BAB28521
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: HYPOTHETICAL PROTEIN (RIKEN CDNA 2810036L13);
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 2810036L13;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P040113-17;
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 1WEX 1 REMARK SEQADV SHEET
REVDAT 2 24-FEB-09 1WEX 1 VERSN
REVDAT 1 25-NOV-04 1WEX 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 BAB28521
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 1WEX COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 28-MAY-04.
REMARK 100 THE DEPOSITION ID IS D_1000023503.
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 : 800 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 VAL A 33 H GLU A 37 1.44
REMARK 500 O GLU A 29 H VAL A 33 1.47
REMARK 500 O LEU A 36 H PHE A 39 1.48
REMARK 500 H VAL A 20 O ALA A 54 1.53
REMARK 500 O ALA A 30 H GLU A 34 1.56
REMARK 500 H ILE A 78 O GLN A 81 1.56
REMARK 500 H HIS A 19 O ASN A 86 1.56
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 -58.56 -169.87
REMARK 500 1 SER A 3 81.97 62.84
REMARK 500 1 SER A 5 82.13 -174.34
REMARK 500 1 SER A 8 153.31 60.86
REMARK 500 1 LYS A 11 155.88 65.15
REMARK 500 1 SER A 13 168.90 55.25
REMARK 500 1 SER A 26 77.58 -118.82
REMARK 500 1 PHE A 50 -73.80 -43.22
REMARK 500 1 ALA A 54 146.45 -170.55
REMARK 500 1 VAL A 68 -70.96 -54.62
REMARK 500 1 ASN A 98 119.71 66.05
REMARK 500 1 SER A 99 153.69 62.76
REMARK 500 2 SER A 8 -57.99 -157.18
REMARK 500 2 SER A 13 -178.13 -64.86
REMARK 500 2 ARG A 52 82.14 48.67
REMARK 500 2 ALA A 54 139.50 -170.97
REMARK 500 2 VAL A 68 -71.67 -57.50
REMARK 500 2 SER A 90 -45.50 -133.49
REMARK 500 2 LYS A 91 -54.61 84.58
REMARK 500 2 ASN A 98 -57.29 -162.48
REMARK 500 2 SER A 99 -62.19 -138.05
REMARK 500 2 SER A 103 -58.85 -178.51
REMARK 500 3 SER A 3 -59.32 -127.67
REMARK 500 3 HIS A 9 -71.29 -80.37
REMARK 500 3 HIS A 10 84.31 54.54
REMARK 500 3 VAL A 14 159.95 -47.10
REMARK 500 3 LEU A 23 -132.19 -82.19
REMARK 500 3 SER A 26 46.80 -95.50
REMARK 500 3 ASP A 31 -33.69 -39.11
REMARK 500 3 PRO A 49 -162.14 -75.01
REMARK 500 3 PHE A 50 -62.59 75.36
REMARK 500 3 ARG A 52 78.05 37.94
REMARK 500 3 ALA A 54 138.30 -175.13
REMARK 500 3 VAL A 68 -70.80 -52.95
REMARK 500 3 SER A 103 87.63 39.60
REMARK 500 4 LYS A 11 70.52 53.33
REMARK 500 4 VAL A 14 158.05 -44.26
REMARK 500 4 SER A 26 73.69 -113.63
REMARK 500 4 ASP A 31 -37.74 -39.63
REMARK 500 4 CYS A 43 -71.41 -58.96
REMARK 500 4 ARG A 52 84.91 47.02
REMARK 500 4 VAL A 68 -71.66 -76.12
REMARK 500 4 THR A 69 -37.42 -38.08
REMARK 500 4 GLN A 82 165.39 -47.90
REMARK 500 4 THR A 89 -31.37 -38.33
REMARK 500 4 LYS A 91 -49.55 85.39
REMARK 500 4 ASN A 98 95.42 65.83
REMARK 500 4 SER A 103 96.97 61.77
REMARK 500 5 SER A 2 -67.11 71.58
REMARK 500 5 SER A 3 106.02 69.56
REMARK 500
REMARK 500 THIS ENTRY HAS 208 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 650
REMARK 650 HELIX
REMARK 650 AUTHOR DETERMINATION METHOD: AUTHOR DETERMINED
REMARK 700
REMARK 700 SHEET
REMARK 700 AUTHOR DETERMINATION METHOD: AUTHOR DETERMINED
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: MMT007008935.1 RELATED DB: TARGETDB
DBREF 1WEX A 8 98 UNP Q921F4 HNRLL_MOUSE 114 204
SEQADV 1WEX GLY A 1 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 2 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 3 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX GLY A 4 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 5 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 6 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX GLY A 7 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 99 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX GLY A 100 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX PRO A 101 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 102 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX SER A 103 UNP Q921F4 CLONING ARTIFACT
SEQADV 1WEX GLY A 104 UNP Q921F4 CLONING ARTIFACT
SEQRES 1 A 104 GLY SER SER GLY SER SER GLY SER HIS HIS LYS VAL SER
SEQRES 2 A 104 VAL SER PRO VAL VAL HIS VAL ARG GLY LEU CYS GLU SER
SEQRES 3 A 104 VAL VAL GLU ALA ASP LEU VAL GLU ALA LEU GLU LYS PHE
SEQRES 4 A 104 GLY THR ILE CYS TYR VAL MET MET MET PRO PHE LYS ARG
SEQRES 5 A 104 GLN ALA LEU VAL GLU PHE GLU ASN ILE ASP SER ALA LYS
SEQRES 6 A 104 GLU CYS VAL THR PHE ALA ALA ASP VAL PRO VAL TYR ILE
SEQRES 7 A 104 ALA GLY GLN GLN ALA PHE PHE ASN TYR SER THR SER LYS
SEQRES 8 A 104 ARG ILE THR ARG PRO GLY ASN SER GLY PRO SER SER GLY
HELIX 1 1 GLU A 29 LEU A 36 1 8
HELIX 2 2 GLU A 37 PHE A 39 1 3
HELIX 3 3 ILE A 61 ASP A 73 1 13
SHEET 1 A 6 VAL A 17 ARG A 21 0
SHEET 2 A 6 ILE A 42 MET A 48 -1 O GLN A 53 N MET A 48
SHEET 3 A 6 GLN A 53 PHE A 58 -1 N VAL A 20 O ALA A 54
SHEET 4 A 6 TYR A 77 ILE A 78 -1 O ASN A 86 N HIS A 19
SHEET 5 A 6 GLN A 81 GLN A 82 0
SHEET 6 A 6 PHE A 84 TYR A 87 0
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