Header list of 2coz.pdb file
Complete list - r 9 2 Bytes
HEADER PROTEIN BINDING 19-MAY-05 2COZ
TITLE SOLUTION STRUCTURE OF THE CAP-GLY DOMAIN IN HUMAN CENTROSOME-
TITLE 2 ASSOCIATED PROTEIN CAP350
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: CENTROSOME-ASSOCIATED PROTEIN 350;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: CAP-GLY DOMAIN;
COMPND 5 SYNONYM: CAP350;
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 HH00807;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P040816-04;
SOURCE 8 OTHER_DETAILS: CELL-FREE PROTEIN SYNTHESIS
KEYWDS MICROTUBULE BINDING, CYTOSKELETON ASSOCIATED PROTEIN, STRUCTURAL
KEYWDS 2 GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND
KEYWDS 3 FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS
KEYWDS 4 INITIATIVE, RSGI, PROTEIN BINDING
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR K.SAITO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA,RIKEN STRUCTURAL
AUTHOR 2 GENOMICS/PROTEOMICS INITIATIVE (RSGI)
REVDAT 3 09-MAR-22 2COZ 1 REMARK SEQADV
REVDAT 2 24-FEB-09 2COZ 1 VERSN
REVDAT 1 19-NOV-05 2COZ 0
JRNL AUTH K.SAITO,S.KOSHIBA,M.INOUE,T.KIGAWA,S.YOKOYAMA
JRNL TITL SOLUTION STRUCTURE OF THE CAP-GLY DOMAIN IN HUMAN
JRNL TITL 2 CENTROSOME-ASSOCIATED PROTEIN CAP350
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, CNS 1.1
REMARK 3 AUTHORS : BRUKER (XWINNMR), BRUNGER, A.T. (CNS)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 2COZ COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 23-MAY-05.
REMARK 100 THE DEPOSITION ID IS D_1000024466.
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 : 1MM PROTEIN, 20MM D-TRIS-HCL,
REMARK 210 PH7.0, 100MM NACL, 1MM D-DTT,
REMARK 210 0.02% NAN3, 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, CNS
REMARK 210 1.1
REMARK 210 METHOD USED : SIMULATED ANNEALING
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 100
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 20
REMARK 210 CONFORMERS, SELECTION CRITERIA : STRUCTURES WITH THE LOWEST
REMARK 210 ENERGY
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 SER A 5 -73.60 -146.52
REMARK 500 1 SER A 6 -175.59 60.23
REMARK 500 1 GLU A 11 79.31 -111.62
REMARK 500 1 THR A 15 36.30 -99.47
REMARK 500 1 SER A 17 63.59 -165.08
REMARK 500 1 LEU A 20 -49.71 -138.42
REMARK 500 1 LEU A 29 59.33 -101.97
REMARK 500 1 VAL A 43 -41.71 -164.76
REMARK 500 1 LYS A 51 107.25 -174.69
REMARK 500 1 CYS A 85 -178.32 -172.81
REMARK 500 1 LYS A 86 -170.20 -60.81
REMARK 500 1 LYS A 97 33.01 -98.10
REMARK 500 1 ASN A 104 43.82 -94.48
REMARK 500 1 PHE A 105 59.06 -142.14
REMARK 500 1 ASP A 106 76.57 -170.18
REMARK 500 1 ASP A 110 59.26 -162.06
REMARK 500 1 ASN A 112 98.97 61.14
REMARK 500 1 GLU A 113 87.89 -166.27
REMARK 500 2 GLN A 12 -66.56 -102.24
REMARK 500 2 GLN A 13 94.32 56.99
REMARK 500 2 VAL A 14 -52.38 -130.90
REMARK 500 2 LEU A 20 -54.50 -133.29
REMARK 500 2 ALA A 21 -45.98 -169.75
REMARK 500 2 ALA A 26 31.09 -162.18
REMARK 500 2 GLU A 28 -65.43 69.47
REMARK 500 2 ASP A 31 30.24 -97.94
REMARK 500 2 VAL A 43 -40.62 -175.09
REMARK 500 2 LYS A 51 104.81 -177.26
REMARK 500 2 PRO A 69 89.32 -52.59
REMARK 500 2 GLU A 70 29.50 -144.93
REMARK 500 2 ASN A 72 33.89 -160.57
REMARK 500 2 TYR A 82 -50.56 -139.90
REMARK 500 2 LYS A 97 37.59 -97.11
REMARK 500 2 PRO A 102 -166.86 -55.66
REMARK 500 2 ASP A 110 99.77 -171.40
REMARK 500 2 ASP A 114 -179.96 -64.89
REMARK 500 3 SER A 5 31.32 -152.38
REMARK 500 3 VAL A 8 93.06 60.16
REMARK 500 3 GLN A 13 29.89 -157.26
REMARK 500 3 VAL A 14 140.67 -179.01
REMARK 500 3 THR A 15 150.75 61.86
REMARK 500 3 GLU A 16 31.25 -141.95
REMARK 500 3 SER A 17 130.55 -172.74
REMARK 500 3 ALA A 21 30.36 -98.41
REMARK 500 3 SER A 22 108.54 59.54
REMARK 500 3 ALA A 26 38.56 -97.47
REMARK 500 3 ASP A 27 -60.17 -129.69
REMARK 500 3 GLU A 28 -78.81 64.17
REMARK 500 3 VAL A 43 -42.09 -165.85
REMARK 500 3 LYS A 51 110.97 -172.08
REMARK 500
REMARK 500 THIS ENTRY HAS 438 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: HSK002100468.1 RELATED DB: TARGETDB
DBREF 2COZ A 8 116 UNP Q8WY20 Q8WY20_HUMAN 2473 2581
SEQADV 2COZ GLY A 1 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 2 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 3 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ GLY A 4 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 5 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 6 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ GLY A 7 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 117 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ GLY A 118 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ PRO A 119 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 120 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ SER A 121 UNP Q8WY20 CLONING ARTIFACT
SEQADV 2COZ GLY A 122 UNP Q8WY20 CLONING ARTIFACT
SEQRES 1 A 122 GLY SER SER GLY SER SER GLY VAL GLU HIS GLU GLN GLN
SEQRES 2 A 122 VAL THR GLU SER PRO SER LEU ALA SER VAL PRO THR ALA
SEQRES 3 A 122 ASP GLU LEU PHE ASP PHE HIS ILE GLY ASP ARG VAL LEU
SEQRES 4 A 122 ILE GLY ASN VAL GLN PRO GLY ILE LEU ARG PHE LYS GLY
SEQRES 5 A 122 GLU THR SER PHE ALA LYS GLY PHE TRP ALA GLY VAL GLU
SEQRES 6 A 122 LEU ASP LYS PRO GLU GLY ASN ASN ASN GLY THR TYR ASP
SEQRES 7 A 122 GLY ILE ALA TYR PHE GLU CYS LYS GLU LYS HIS GLY ILE
SEQRES 8 A 122 PHE ALA PRO PRO GLN LYS ILE SER HIS ILE PRO GLU ASN
SEQRES 9 A 122 PHE ASP ASP TYR VAL ASP ILE ASN GLU ASP GLU ASP SER
SEQRES 10 A 122 GLY PRO SER SER GLY
HELIX 1 1 PRO A 94 GLN A 96 5 3
SHEET 1 A 5 GLY A 90 ALA A 93 0
SHEET 2 A 5 PHE A 60 LEU A 66 -1 N VAL A 64 O ILE A 91
SHEET 3 A 5 GLN A 44 GLU A 53 -1 N ILE A 47 O GLU A 65
SHEET 4 A 5 ASP A 36 ILE A 40 -1 N ASP A 36 O LEU A 48
SHEET 5 A 5 ILE A 98 SER A 99 -1 O SER A 99 N LEU A 39
SHEET 1 B 2 THR A 76 TYR A 77 0
SHEET 2 B 2 ILE A 80 ALA A 81 -1 O ILE A 80 N TYR A 77
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