Header list of 1wie.pdb file
Complete list - r 2 2 Bytes
HEADER PROTEIN BINDING 28-MAY-04 1WIE TITLE SOLUTION STRUCTURE OF THE FIRST SH3 DOMAIN OF KIAA0318 PROTEIN COMPND MOL_ID: 1; COMPND 2 MOLECULE: RIM BINDING PROTEIN 2; COMPND 3 CHAIN: A; COMPND 4 FRAGMENT: SH3 DOMAIN; COMPND 5 SYNONYM: KIAA0318 PROTEIN, RIM-BP2; COMPND 6 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: KAZUSA CDNA HG00364; SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID; SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P030512-61; SOURCE 8 OTHER_DETAILS: CELL-FREE PROTEIN SYNTHESIS KEYWDS BETA BARREL, RIM-BINDING PROTEIN 2, KIAA0318 PROTEIN, STRUCTURAL KEYWDS 2 GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, KEYWDS 3 PROTEIN BINDING EXPDTA SOLUTION NMR NUMMDL 20 AUTHOR K.INOUE,F.HAYASHI,S.YOKOYAMA,RIKEN STRUCTURAL GENOMICS/PROTEOMICS AUTHOR 2 INITIATIVE (RSGI) REVDAT 3 02-MAR-22 1WIE 1 REMARK SEQADV REVDAT 2 24-FEB-09 1WIE 1 VERSN REVDAT 1 28-NOV-04 1WIE 0 JRNL AUTH K.INOUE,F.HAYASHI,S.YOKOYAMA JRNL TITL SOLUTION STRUCTURE OF THE FIRST SH3 DOMAIN OF KIAA0318 JRNL TITL 2 PROTEIN JRNL REF TO BE PUBLISHED JRNL REFN REMARK 2 REMARK 2 RESOLUTION. NOT APPLICABLE. REMARK 3 REMARK 3 REFINEMENT. REMARK 3 PROGRAM : VNMR 6.1C, CYANA 1.0.7 REMARK 3 AUTHORS : VARIAN (VNMR), GUENTERT, P. (CYANA) REMARK 3 REMARK 3 OTHER REFINEMENT REMARKS: NULL REMARK 4 REMARK 4 1WIE COMPLIES WITH FORMAT V. 3.15, 01-DEC-08 REMARK 100 REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 08-JUN-04. REMARK 100 THE DEPOSITION ID IS D_1000023613. REMARK 210 REMARK 210 EXPERIMENTAL DETAILS REMARK 210 EXPERIMENT TYPE : NMR REMARK 210 TEMPERATURE (KELVIN) : 298 REMARK 210 PH : 6.0 REMARK 210 IONIC STRENGTH : 120MM REMARK 210 PRESSURE : AMBIENT REMARK 210 SAMPLE CONTENTS : 1.26MM 13C, 15N-LABELED PROTEIN; REMARK 210 20MM PINA; 100MM NACL; 1MM D-DTT; REMARK 210 0.02% NAN3 REMARK 210 REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_13C-SEPARATED_NOESY; 3D_15N REMARK 210 -SEPARATED_NOESY REMARK 210 SPECTROMETER FIELD STRENGTH : 800 MHZ REMARK 210 SPECTROMETER MODEL : INOVA REMARK 210 SPECTROMETER MANUFACTURER : VARIAN REMARK 210 REMARK 210 STRUCTURE DETERMINATION. REMARK 210 SOFTWARE USED : NMRPIPE 20020425, NMRVIEW 5.0.4, REMARK 210 KUJIRA 0.8992, CYANA 1.0.7 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 H TYR A 26 O LEU A 42 1.55 REMARK 500 H TYR A 60 O VAL A 72 1.56 REMARK 500 O ALA A 38 H LEU A 71 1.57 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 85.51 54.65 REMARK 500 1 SER A 5 -68.67 71.79 REMARK 500 1 SER A 6 159.64 66.32 REMARK 500 1 SER A 9 105.19 -51.13 REMARK 500 1 ARG A 12 43.65 -93.74 REMARK 500 1 TYR A 13 50.22 -170.54 REMARK 500 1 SER A 14 -33.68 174.13 REMARK 500 1 LYS A 16 154.41 -40.09 REMARK 500 1 ALA A 22 123.41 -35.86 REMARK 500 1 PHE A 29 30.95 -87.21 REMARK 500 1 ASN A 33 118.74 -39.71 REMARK 500 1 ALA A 44 117.01 -33.78 REMARK 500 1 MET A 54 142.68 -37.48 REMARK 500 1 LEU A 64 153.09 -41.47 REMARK 500 1 PHE A 79 88.27 -50.18 REMARK 500 1 SER A 85 106.77 -40.65 REMARK 500 1 ARG A 86 -55.16 -133.58 REMARK 500 1 SER A 89 132.70 64.84 REMARK 500 2 SER A 3 110.30 -166.15 REMARK 500 2 SER A 5 -58.55 -126.10 REMARK 500 2 SER A 14 21.14 -147.19 REMARK 500 2 ASN A 33 121.91 -37.27 REMARK 500 2 ALA A 44 116.49 -34.72 REMARK 500 2 LEU A 64 146.80 -39.74 REMARK 500 2 PHE A 79 91.46 -47.89 REMARK 500 2 GLN A 81 -144.15 -75.45 REMARK 500 2 ASP A 82 -45.90 84.39 REMARK 500 2 ASN A 83 91.37 -160.12 REMARK 500 2 SER A 89 147.55 174.98 REMARK 500 3 SER A 9 86.06 46.51 REMARK 500 3 ARG A 12 38.86 -93.14 REMARK 500 3 TYR A 13 58.37 -175.96 REMARK 500 3 SER A 14 -38.95 -173.96 REMARK 500 3 LYS A 16 151.99 -39.69 REMARK 500 3 ALA A 22 127.56 -38.46 REMARK 500 3 PHE A 29 31.71 -87.63 REMARK 500 3 ASN A 33 120.84 -39.38 REMARK 500 3 ALA A 44 118.06 -34.75 REMARK 500 3 MET A 54 159.64 -44.21 REMARK 500 3 GLU A 61 60.85 -69.99 REMARK 500 3 PHE A 79 92.33 -47.02 REMARK 500 3 GLN A 81 -127.01 -120.64 REMARK 500 3 ASP A 82 -65.25 69.42 REMARK 500 3 SER A 85 54.98 -91.34 REMARK 500 3 LEU A 87 170.08 -46.68 REMARK 500 3 THR A 90 -42.84 -176.75 REMARK 500 3 SER A 94 -57.78 -168.52 REMARK 500 4 SER A 5 160.02 61.51 REMARK 500 4 SER A 6 -61.44 -173.70 REMARK 500 4 SER A 9 120.68 179.00 REMARK 500 REMARK 500 THIS ENTRY HAS 359 RAMACHANDRAN OUTLIERS. REMARK 500 REMARK 500 REMARK: NULL REMARK 900 REMARK 900 RELATED ENTRIES REMARK 900 RELATED ID: HSK002000310.1 RELATED DB: TARGETDB DBREF 1WIE A 8 90 UNP O15034 RIMB2_HUMAN 160 242 SEQADV 1WIE GLY A 1 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 2 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 3 UNP O15034 CLONING ARTIFACT SEQADV 1WIE GLY A 4 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 5 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 6 UNP O15034 CLONING ARTIFACT SEQADV 1WIE GLY A 7 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 91 UNP O15034 CLONING ARTIFACT SEQADV 1WIE GLY A 92 UNP O15034 CLONING ARTIFACT SEQADV 1WIE PRO A 93 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 94 UNP O15034 CLONING ARTIFACT SEQADV 1WIE SER A 95 UNP O15034 CLONING ARTIFACT SEQADV 1WIE GLY A 96 UNP O15034 CLONING ARTIFACT SEQRES 1 A 96 GLY SER SER GLY SER SER GLY THR SER LYS GLN ARG TYR SEQRES 2 A 96 SER GLY LYS VAL HIS LEU CYS VAL ALA ARG TYR SER TYR SEQRES 3 A 96 ASN PRO PHE ASP GLY PRO ASN GLU ASN PRO GLU ALA GLU SEQRES 4 A 96 LEU PRO LEU THR ALA GLY LYS TYR LEU TYR VAL TYR GLY SEQRES 5 A 96 ASP MET ASP GLU ASP GLY PHE TYR GLU GLY GLU LEU LEU SEQRES 6 A 96 ASP GLY GLN ARG GLY LEU VAL PRO SER ASN PHE VAL ASP SEQRES 7 A 96 PHE VAL GLN ASP ASN GLU SER ARG LEU ALA SER THR SER SEQRES 8 A 96 GLY PRO SER SER GLY HELIX 1 1 ASN A 27 GLY A 31 5 5 SHEET 1 A 4 GLU A 61 LEU A 64 0 SHEET 2 A 4 TYR A 47 TYR A 51 -1 N TYR A 51 O GLU A 61 SHEET 3 A 4 VAL A 17 ALA A 22 -1 N HIS A 18 O VAL A 50 SHEET 4 A 4 VAL A 77 ASP A 78 -1 O ASP A 78 N VAL A 21 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