Header list of 2cuq.pdb file
Complete list - r 9 2 Bytes
HEADER STRUCTURAL GENOMICS, UNKNOWN FUNCTION 27-MAY-05 2CUQ TITLE SOLUTION STRUCTURE OF SECOND LIM DOMAIN FROM HUMAN SKELETAL MUSCLE TITLE 2 LIM-PROTEIN 2 COMPND MOL_ID: 1; COMPND 2 MOLECULE: FOUR AND A HALF LIM DOMAINS 3; COMPND 3 CHAIN: A; COMPND 4 FRAGMENT: LIM DOMAIN; COMPND 5 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: FHL3; SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID; SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P040830-08; SOURCE 8 OTHER_DETAILS: CELL-FREE PROTEIN SYNTHESIS KEYWDS FOUR AND A HALF LIM DOMAINS 3, LIM DOMAIN, STRUCTURAL GENOMICS, KEYWDS 2 NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL KEYWDS 3 ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, KEYWDS 4 UNKNOWN FUNCTION EXPDTA SOLUTION NMR NUMMDL 20 AUTHOR T.N.NIRAULA,K.SAITO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA,RIKEN AUTHOR 2 STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE (RSGI) REVDAT 3 09-MAR-22 2CUQ 1 REMARK SEQADV LINK REVDAT 2 24-FEB-09 2CUQ 1 VERSN REVDAT 1 27-NOV-05 2CUQ 0 JRNL AUTH T.N.NIRAULA,K.SAITO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA JRNL TITL SOLUTION STRUCTURE OF SECOND LIM DOMAIN FROM HUMAN SKELETAL JRNL TITL 2 MUSCLE LIM-PROTEIN 2 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), GUNTERT, P. (CYANA) REMARK 3 REMARK 3 OTHER REFINEMENT REMARKS: NULL REMARK 4 REMARK 4 2CUQ COMPLIES WITH FORMAT V. 3.15, 01-DEC-08 REMARK 100 REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 06-JUN-05. REMARK 100 THE DEPOSITION ID IS D_1000024641. 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 : 120 REMARK 210 PRESSURE : AMBIENT REMARK 210 SAMPLE CONTENTS : 1.40MM LIM DOMAIN U-13C 15N; REMARK 210 20MM D-TRIS-HCL; 100MM NACL; 1 REMARK 210 MM D-DTT; 0.02% NAN3; 0.01MM REMARK 210 ZNCL2; 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 20031121, NMRVIEW 5.0.4, REMARK 210 KUJIRA 0.913, 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 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 LYS A 23 -75.23 -94.67 REMARK 500 1 THR A 24 146.40 -173.53 REMARK 500 1 GLN A 27 47.75 -83.03 REMARK 500 1 LEU A 42 93.58 -47.75 REMARK 500 1 ALA A 52 99.65 -44.74 REMARK 500 1 GLU A 71 -38.10 -134.97 REMARK 500 1 ALA A 74 41.02 -86.64 REMARK 500 1 SER A 75 174.82 -58.80 REMARK 500 2 ASN A 12 42.80 -85.16 REMARK 500 2 ARG A 20 -62.65 -90.90 REMARK 500 2 LYS A 23 -71.70 -100.30 REMARK 500 2 THR A 26 -61.93 -129.31 REMARK 500 2 ARG A 39 -39.31 -38.52 REMARK 500 2 LEU A 42 101.26 -50.56 REMARK 500 2 ALA A 52 104.26 -46.23 REMARK 500 2 GLU A 71 -39.66 -132.46 REMARK 500 2 SER A 75 42.59 -105.75 REMARK 500 3 SER A 2 42.57 -81.17 REMARK 500 3 TYR A 10 109.24 -48.12 REMARK 500 3 LYS A 23 -75.82 -91.90 REMARK 500 3 THR A 24 145.18 -171.63 REMARK 500 3 LEU A 42 89.40 -49.42 REMARK 500 3 ALA A 52 98.42 -45.13 REMARK 500 3 GLU A 71 -42.59 -135.01 REMARK 500 4 SER A 3 110.66 -160.90 REMARK 500 4 SER A 6 -52.55 -130.83 REMARK 500 4 LYS A 23 -75.84 -95.85 REMARK 500 4 ARG A 39 -39.86 -38.77 REMARK 500 4 LEU A 42 88.70 -52.41 REMARK 500 4 ALA A 52 97.34 -46.57 REMARK 500 4 GLU A 71 -38.25 -134.90 REMARK 500 4 PRO A 77 -174.61 -69.79 REMARK 500 5 ALA A 15 148.68 -172.78 REMARK 500 5 LYS A 23 -72.72 -102.16 REMARK 500 5 ARG A 39 -37.57 -34.47 REMARK 500 5 LEU A 42 103.63 -52.47 REMARK 500 5 ALA A 52 99.14 -47.78 REMARK 500 5 GLU A 71 -47.18 -134.30 REMARK 500 6 SER A 5 120.32 -172.87 REMARK 500 6 SER A 22 49.75 70.01 REMARK 500 6 LYS A 23 -75.86 -99.93 REMARK 500 6 LEU A 42 87.58 -48.88 REMARK 500 6 CYS A 44 158.75 -48.76 REMARK 500 6 ALA A 52 100.98 -45.85 REMARK 500 6 GLU A 71 -35.22 -135.02 REMARK 500 7 SER A 6 42.95 -80.71 REMARK 500 7 ASN A 12 146.72 -173.08 REMARK 500 7 ALA A 15 148.40 -175.00 REMARK 500 7 SER A 22 44.75 72.09 REMARK 500 7 LYS A 23 -75.22 -94.18 REMARK 500 REMARK 500 THIS ENTRY HAS 177 RAMACHANDRAN OUTLIERS. REMARK 500 REMARK 500 REMARK: NULL REMARK 620 REMARK 620 METAL COORDINATION REMARK 620 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER; REMARK 620 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE): REMARK 620 REMARK 620 COORDINATION ANGLES FOR: M RES CSSEQI METAL REMARK 620 ZN A 201 ZN REMARK 620 N RES CSSEQI ATOM REMARK 620 1 CYS A 18 SG REMARK 620 2 CYS A 21 SG 120.4 REMARK 620 3 HIS A 38 ND1 86.5 113.6 REMARK 620 4 CYS A 41 SG 114.9 107.1 113.5 REMARK 620 N 1 2 3 REMARK 620 REMARK 620 COORDINATION ANGLES FOR: M RES CSSEQI METAL REMARK 620 ZN A 401 ZN REMARK 620 N RES CSSEQI ATOM REMARK 620 1 CYS A 44 SG REMARK 620 2 CYS A 47 SG 103.2 REMARK 620 3 CYS A 65 SG 116.7 111.0 REMARK 620 4 CYS A 68 SG 86.0 118.7 117.9 REMARK 620 N 1 2 3 REMARK 800 REMARK 800 SITE REMARK 800 SITE_IDENTIFIER: AC1 REMARK 800 EVIDENCE_CODE: SOFTWARE REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE ZN A 201 REMARK 800 REMARK 800 SITE_IDENTIFIER: AC2 REMARK 800 EVIDENCE_CODE: SOFTWARE REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE ZN A 401 REMARK 900 REMARK 900 RELATED ENTRIES REMARK 900 RELATED ID: HSI002003711.2 RELATED DB: TARGETDB DBREF 2CUQ A 8 74 UNP Q13643 FHL3_HUMAN 152 218 SEQADV 2CUQ GLY A 1 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 2 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 3 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ GLY A 4 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 5 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 6 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ GLY A 7 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 75 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ GLY A 76 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ PRO A 77 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 78 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ SER A 79 UNP Q13643 CLONING ARTIFACT SEQADV 2CUQ GLY A 80 UNP Q13643 CLONING ARTIFACT SEQRES 1 A 80 GLY SER SER GLY SER SER GLY PRO CYS TYR GLU ASN LYS SEQRES 2 A 80 PHE ALA PRO ARG CYS ALA ARG CYS SER LYS THR LEU THR SEQRES 3 A 80 GLN GLY GLY VAL THR TYR ARG ASP GLN PRO TRP HIS ARG SEQRES 4 A 80 GLU CYS LEU VAL CYS THR GLY CYS GLN THR PRO LEU ALA SEQRES 5 A 80 GLY GLN GLN PHE THR SER ARG ASP GLU ASP PRO TYR CYS SEQRES 6 A 80 VAL ALA CYS PHE GLY GLU LEU PHE ALA SER GLY PRO SER SEQRES 7 A 80 SER GLY HET ZN A 201 1 HET ZN A 401 1 HETNAM ZN ZINC ION FORMUL 2 ZN 2(ZN 2+) HELIX 1 1 VAL A 66 PHE A 73 1 8 SHEET 1 A 2 VAL A 30 THR A 31 0 SHEET 2 A 2 PRO A 36 TRP A 37 -1 O TRP A 37 N VAL A 30 SHEET 1 B 2 PHE A 56 SER A 58 0 SHEET 2 B 2 PRO A 63 CYS A 65 -1 O TYR A 64 N THR A 57 LINK SG CYS A 18 ZN ZN A 201 1555 1555 2.32 LINK SG CYS A 21 ZN ZN A 201 1555 1555 2.31 LINK ND1 HIS A 38 ZN ZN A 201 1555 1555 2.37 LINK SG CYS A 41 ZN ZN A 201 1555 1555 2.30 LINK SG CYS A 44 ZN ZN A 401 1555 1555 2.37 LINK SG CYS A 47 ZN ZN A 401 1555 1555 2.33 LINK SG CYS A 65 ZN ZN A 401 1555 1555 2.33 LINK SG CYS A 68 ZN ZN A 401 1555 1555 2.33 SITE 1 AC1 4 CYS A 18 CYS A 21 HIS A 38 CYS A 41 SITE 1 AC2 4 CYS A 44 CYS A 47 CYS A 65 CYS A 68 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