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HEADER TRANSFERASE 25-NOV-03 1V5S TITLE SOLUTION STRUCTURE OF KINASE ASSOCIATED DOMAIN 1 OF MOUSE TITLE 2 MAP/MICROTUBULE AFFINITY-REGULATING KINASE 3 COMPND MOL_ID: 1; COMPND 2 MOLECULE: MAP/MICROTUBULE AFFINITY-REGULATING KINASE 3; COMPND 3 CHAIN: A; COMPND 4 FRAGMENT: KINASE ASSOCIATED DOMAIN 1; COMPND 5 EC: 2.7.1.27; 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: RIKEN CDNA 1600015G02; SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID; SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P020417-25; SOURCE 8 OTHER_DETAILS: CELL-FREE PROTEIN SYNTHESIS KEYWDS KA1 DOMAIN, ELKL MOTIF, MARK3, PHOSPHORYLATION, STRUCTURAL GENOMICS, KEYWDS 2 NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL KEYWDS 3 ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, KEYWDS 4 TRANSFERASE EXPDTA SOLUTION NMR NUMMDL 20 AUTHOR N.TOCHIO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA,RIKEN STRUCTURAL AUTHOR 2 GENOMICS/PROTEOMICS INITIATIVE (RSGI) REVDAT 4 02-MAR-22 1V5S 1 REMARK SEQADV REVDAT 3 24-FEB-09 1V5S 1 VERSN REVDAT 2 29-AUG-06 1V5S 1 AUTHOR KEYWDS DBREF SEQADV REVDAT 2 2 1 REMARK REVDAT 1 25-MAY-04 1V5S 0 JRNL AUTH N.TOCHIO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA JRNL TITL SOLUTION STRUCTURE OF KINASE ASSOCIATED DOMAIN 1 OF MOUSE JRNL TITL 2 MAP/MICROTUBULE AFFINITY-REGULATING KINASE 3 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), GUENTERT, P. (CYANA) REMARK 3 REMARK 3 OTHER REFINEMENT REMARKS: NULL REMARK 4 REMARK 4 1V5S COMPLIES WITH FORMAT V. 3.15, 01-DEC-08 REMARK 100 REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 28-NOV-03. REMARK 100 THE DEPOSITION ID IS D_1000006241. 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 : 2.0MM KA1 DOMAIN U-15N, 13C; REMARK 210 20MM PHOSPHATE BUFFER NA; 100MM REMARK 210 NACL; 1MM D-DTT; 0.02% NAN3; 10% REMARK 210 D2O 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 : 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 0.853, 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 : STRUCTURES WITH THE LEAST REMARK 210 RESTRAINT VIOLATIONS, 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: 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 20 68.79 -105.90 REMARK 500 1 PRO A 25 -178.23 -69.75 REMARK 500 1 THR A 27 172.22 -53.44 REMARK 500 1 ASN A 53 41.75 -97.05 REMARK 500 1 ASN A 54 43.10 39.69 REMARK 500 1 ASP A 71 -60.37 -105.40 REMARK 500 1 ASN A 93 105.36 -36.70 REMARK 500 1 ASN A 109 -36.53 -36.75 REMARK 500 1 LYS A 119 34.95 36.13 REMARK 500 2 LEU A 5 43.86 -93.75 REMARK 500 2 ILE A 6 147.86 -38.29 REMARK 500 2 TYR A 22 -69.10 -128.41 REMARK 500 2 THR A 26 39.53 -92.16 REMARK 500 2 ASN A 53 39.30 -99.02 REMARK 500 2 PHE A 63 56.06 -106.98 REMARK 500 3 HIS A 4 117.54 -163.80 REMARK 500 3 GLU A 28 69.25 -103.48 REMARK 500 3 MET A 43 -35.67 -35.95 REMARK 500 3 GLU A 45 -36.09 -39.99 REMARK 500 3 ARG A 47 -39.24 -34.52 REMARK 500 3 ASN A 53 38.36 -94.48 REMARK 500 3 ASP A 71 -50.37 -131.57 REMARK 500 3 CYS A 85 175.82 -52.53 REMARK 500 3 LEU A 90 48.44 39.31 REMARK 500 3 LEU A 92 -175.03 -175.23 REMARK 500 3 SER A 121 -175.19 -55.32 REMARK 500 3 PRO A 123 95.83 -69.80 REMARK 500 3 SER A 124 151.42 -41.75 REMARK 500 4 HIS A 16 142.09 -35.14 REMARK 500 4 PRO A 25 -179.34 -69.70 REMARK 500 4 THR A 27 163.52 -48.38 REMARK 500 4 ASN A 53 36.21 -92.72 REMARK 500 4 SER A 91 31.37 37.01 REMARK 500 4 ASN A 93 173.38 -47.31 REMARK 500 4 LYS A 119 38.34 37.30 REMARK 500 4 PRO A 123 85.00 -69.76 REMARK 500 5 ASN A 8 123.23 -172.87 REMARK 500 5 HIS A 14 106.23 -162.91 REMARK 500 5 PRO A 25 -167.82 -69.73 REMARK 500 5 THR A 26 43.44 -98.80 REMARK 500 5 GLU A 28 42.66 -83.26 REMARK 500 5 ASN A 53 41.97 -95.49 REMARK 500 5 ASN A 54 42.03 39.05 REMARK 500 5 LEU A 87 159.12 -43.06 REMARK 500 5 LEU A 90 32.41 34.32 REMARK 500 6 LYS A 11 51.10 37.12 REMARK 500 6 TYR A 22 -62.57 -131.32 REMARK 500 6 ILE A 24 137.37 -38.19 REMARK 500 6 PRO A 25 -163.84 -69.77 REMARK 500 6 MET A 43 -34.25 -34.38 REMARK 500 REMARK 500 THIS ENTRY HAS 202 RAMACHANDRAN OUTLIERS. REMARK 500 REMARK 500 REMARK: NULL REMARK 900 REMARK 900 RELATED ENTRIES REMARK 900 RELATED ID: 1UL7 RELATED DB: PDB REMARK 900 ANOTHER CONSTRUCT OF THE SAME PROTEIN. REMARK 900 RELATED ID: MMT007019316.2 RELATED DB: TARGETDB DBREF 1V5S A 41 120 UNP Q03141 MARK3_MOUSE 674 753 SEQADV 1V5S MET A 1 UNP Q03141 SEE REMARK 999 SEQADV 1V5S LYS A 2 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASP A 3 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 4 UNP Q03141 SEE REMARK 999 SEQADV 1V5S LEU A 5 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ILE A 6 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 7 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASN A 8 UNP Q03141 SEE REMARK 999 SEQADV 1V5S VAL A 9 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 10 UNP Q03141 SEE REMARK 999 SEQADV 1V5S LYS A 11 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLU A 12 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLU A 13 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 14 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ALA A 15 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 16 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ALA A 17 UNP Q03141 SEE REMARK 999 SEQADV 1V5S HIS A 18 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASN A 19 UNP Q03141 SEE REMARK 999 SEQADV 1V5S LYS A 20 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASP A 21 UNP Q03141 SEE REMARK 999 SEQADV 1V5S TYR A 22 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASP A 23 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ILE A 24 UNP Q03141 SEE REMARK 999 SEQADV 1V5S PRO A 25 UNP Q03141 SEE REMARK 999 SEQADV 1V5S THR A 26 UNP Q03141 SEE REMARK 999 SEQADV 1V5S THR A 27 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLU A 28 UNP Q03141 SEE REMARK 999 SEQADV 1V5S ASN A 29 UNP Q03141 SEE REMARK 999 SEQADV 1V5S LEU A 30 UNP Q03141 SEE REMARK 999 SEQADV 1V5S TYR A 31 UNP Q03141 SEE REMARK 999 SEQADV 1V5S PHE A 32 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLN A 33 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLY A 34 UNP Q03141 SEE REMARK 999 SEQADV 1V5S SER A 35 UNP Q03141 SEE REMARK 999 SEQADV 1V5S SER A 36 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLY A 37 UNP Q03141 SEE REMARK 999 SEQADV 1V5S SER A 38 UNP Q03141 SEE REMARK 999 SEQADV 1V5S SER A 39 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLY A 40 UNP Q03141 SEE REMARK 999 SEQADV 1V5S GLY A 51 UNP Q03141 ASP 684 CONFLICT SEQADV 1V5S SER A 121 UNP Q03141 CLONING ARTIFACT SEQADV 1V5S GLY A 122 UNP Q03141 CLONING ARTIFACT SEQADV 1V5S PRO A 123 UNP Q03141 CLONING ARTIFACT SEQADV 1V5S SER A 124 UNP Q03141 CLONING ARTIFACT SEQADV 1V5S SER A 125 UNP Q03141 CLONING ARTIFACT SEQADV 1V5S GLY A 126 UNP Q03141 CLONING ARTIFACT SEQRES 1 A 126 MET LYS ASP HIS LEU ILE HIS ASN VAL HIS LYS GLU GLU SEQRES 2 A 126 HIS ALA HIS ALA HIS ASN LYS ASP TYR ASP ILE PRO THR SEQRES 3 A 126 THR GLU ASN LEU TYR PHE GLN GLY SER SER GLY SER SER SEQRES 4 A 126 GLY ASP MET MET ARG GLU ILE ARG LYS VAL LEU GLY ALA SEQRES 5 A 126 ASN ASN CYS ASP TYR GLU GLN ARG GLU ARG PHE LEU LEU SEQRES 6 A 126 PHE CYS VAL HIS GLY ASP GLY HIS ALA GLU ASN LEU VAL SEQRES 7 A 126 GLN TRP GLU MET GLU VAL CYS LYS LEU PRO ARG LEU SER SEQRES 8 A 126 LEU ASN GLY VAL ARG PHE LYS ARG ILE SER GLY THR SER SEQRES 9 A 126 ILE ALA PHE LYS ASN ILE ALA SER LYS ILE ALA ASN GLU SEQRES 10 A 126 LEU LYS LEU SER GLY PRO SER SER GLY HELIX 1 1 SER A 38 ASN A 53 1 16 HELIX 2 2 THR A 103 LEU A 118 1 16 SHEET 1 A 5 ASN A 29 LEU A 30 0 SHEET 2 A 5 ARG A 96 SER A 101 -1 O PHE A 97 N LEU A 30 SHEET 3 A 5 VAL A 78 GLU A 83 -1 N GLN A 79 O ILE A 100 SHEET 4 A 5 LEU A 64 HIS A 69 -1 N CYS A 67 O TRP A 80 SHEET 5 A 5 CYS A 55 GLU A 61 -1 N GLU A 61 O LEU A 64 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