Header list of 1j6q.pdb file
Complete list - 23 20 Bytes
HEADER CHAPERONE 30-APR-02 1J6Q
TITLE SOLUTION STRUCTURE AND CHARACTERIZATION OF THE HEME CHAPERONE CCME
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: CYTOCHROME C MATURATION PROTEIN E;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: WATER SOLUBLE DOMAIN OF CCME;
COMPND 5 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: SHEWANELLA PUTREFACIENS;
SOURCE 3 ORGANISM_TAXID: 24;
SOURCE 4 GENE: CCME;
SOURCE 5 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE 6 EXPRESSION_SYSTEM_TAXID: 562;
SOURCE 7 EXPRESSION_SYSTEM_STRAIN: BL21 GOLD(DE3);
SOURCE 8 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 9 EXPRESSION_SYSTEM_PLASMID: PPB10
KEYWDS ALL-BETA PROTEIN, HEME DELIVERY, CYTOCHROME C MATURATION, OB-
KEYWDS 2 (OLIGONUCLEOTIDE BINDING)FOLD, CHAPERONE
EXPDTA SOLUTION NMR
MDLTYP MINIMIZED AVERAGE
AUTHOR F.ARNESANO,L.BANCI,P.D.BARKER,I.BERTINI,A.ROSATO,X.C.SU,M.S.VIEZZOLI
REVDAT 3 23-FEB-22 1J6Q 1 REMARK SEQADV
REVDAT 2 24-FEB-09 1J6Q 1 VERSN
REVDAT 1 25-DEC-02 1J6Q 0
JRNL AUTH F.ARNESANO,L.BANCI,P.D.BARKER,I.BERTINI,A.ROSATO,X.C.SU,
JRNL AUTH 2 M.S.VIEZZOLI
JRNL TITL SOLUTION STRUCTURE AND CHARACTERIZATION OF THE HEME
JRNL TITL 2 CHAPERONE CCME
JRNL REF BIOCHEMISTRY V. 41 13587 2002
JRNL REFN ISSN 0006-2960
JRNL PMID 12427019
JRNL DOI 10.1021/BI026362W
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : XWINNMR 2.6, AMBER 5.0
REMARK 3 AUTHORS : BRUKER (XWINNMR), PEARLMAN, CASE, CALDWELL, ROSS,
REMARK 3 CHEATHAM, FERGUSON, SEIBEL, SINGH, WEINER, KOLLMAN
REMARK 3 (AMBER)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: 1866 MEANINGFUL NOES AND 89 DIHEDRAL
REMARK 3 ANGLE CONSTRAINTS.
REMARK 4
REMARK 4 1J6Q COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 01-MAY-02.
REMARK 100 THE DEPOSITION ID IS D_1000016066.
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 : 20 MM PHOSPHATE
REMARK 210 PRESSURE : 1 ATM
REMARK 210 SAMPLE CONTENTS : 2.0 MM APOCCME, 20 MM PHOSPHATE,
REMARK 210 90% H2O, 10% D2O
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 2D NOESY; 2D TOCSY; 3D_13C
REMARK 210 -SEPARATED_NOESY; 3D_15N-
REMARK 210 SEPARATED_NOESY; HNHA; HNCO;
REMARK 210 HNHB; CBCANH; CC(CO)NH; CBCA(CO)
REMARK 210 NH
REMARK 210 SPECTROMETER FIELD STRENGTH : 700 MHZ
REMARK 210 SPECTROMETER MODEL : AVANCE
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : XEASY 1.3, DYANA 1.5, CORMA
REMARK 210 METHOD USED : SIMULATED ANNEALING, TORSION
REMARK 210 ANGLE DYANAMICS, RESTRAINED
REMARK 210 ENERGY MINIMIZATION
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : NULL
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 1
REMARK 210 CONFORMERS, SELECTION CRITERIA : NULL
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 1
REMARK 210
REMARK 210 REMARK: THE STRUCTURE WAS DETERMINED USING TRIPLE-RESONANCE NMR
REMARK 210 SPECTROSCOPY ON 13C AND 15N DOUBLE LABELED APOCCME.
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 465
REMARK 465 MISSING RESIDUES
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE
REMARK 465 EXPERIMENT. (RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 465 SSSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)
REMARK 465 RES C SSSEQI
REMARK 465 PHE A 26
REMARK 465 ALA A 27
REMARK 465 ALA A 28
REMARK 465 ASP A 29
REMARK 465 LEU A 30
REMARK 465 ASN A 31
REMARK 465 ASP A 132
REMARK 465 GLU A 133
REMARK 465 ASN A 134
REMARK 465 TYR A 135
REMARK 465 MET A 136
REMARK 465 PRO A 137
REMARK 465 PRO A 138
REMARK 465 GLU A 139
REMARK 465 VAL A 140
REMARK 465 ALA A 141
REMARK 465 GLU A 142
REMARK 465 ALA A 143
REMARK 465 MET A 144
REMARK 465 GLY A 145
REMARK 465 GLN A 146
REMARK 465 LYS A 147
REMARK 465 HIS A 148
REMARK 465 GLU A 149
REMARK 465 LYS A 150
REMARK 465 LEU A 151
REMARK 465 ASP A 152
REMARK 465 TYR A 153
REMARK 465 SER A 154
REMARK 465 GLN A 155
REMARK 465 GLN A 156
REMARK 465 LYS A 157
REMARK 465 SER A 158
REMARK 465 ALA A 159
REMARK 465 THR A 160
REMARK 465 GLN A 161
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: COVALENT BOND ANGLES
REMARK 500
REMARK 500 THE STEREOCHEMICAL PARAMETERS OF THE FOLLOWING RESIDUES
REMARK 500 HAVE VALUES WHICH DEVIATE FROM EXPECTED VALUES BY MORE
REMARK 500 THAN 6*RMSD (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 500 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT: (10X,I3,1X,A3,1X,A1,I4,A1,3(1X,A4,2X),12X,F5.1)
REMARK 500
REMARK 500 EXPECTED VALUES PROTEIN: ENGH AND HUBER, 1999
REMARK 500 EXPECTED VALUES NUCLEIC ACID: CLOWNEY ET AL 1996
REMARK 500
REMARK 500 M RES CSSEQI ATM1 ATM2 ATM3
REMARK 500 ARG A 61 NE - CZ - NH2 ANGL. DEV. = -3.1 DEGREES
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 ILE A 43 42.13 -79.44
REMARK 500 VAL A 44 -55.16 -141.86
REMARK 500 LYS A 47 -107.47 -149.52
REMARK 500 LYS A 53 -74.80 -102.94
REMARK 500 LEU A 78 7.00 -154.88
REMARK 500 PRO A 101 -92.44 -64.37
REMARK 500 ASP A 102 43.19 -77.93
REMARK 500 LEU A 103 13.05 50.23
REMARK 500 PHE A 104 79.44 59.52
REMARK 500 ASP A 119 67.29 13.52
REMARK 500 THR A 125 -40.32 -147.35
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: PLANAR GROUPS
REMARK 500
REMARK 500 PLANAR GROUPS IN THE FOLLOWING RESIDUES HAVE A TOTAL
REMARK 500 RMS DISTANCE OF ALL ATOMS FROM THE BEST-FIT PLANE
REMARK 500 BY MORE THAN AN EXPECTED VALUE OF 6*RMSD, WITH AN
REMARK 500 RMSD 0.02 ANGSTROMS, OR AT LEAST ONE ATOM HAS
REMARK 500 AN RMSD GREATER THAN THIS VALUE
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 M RES CSSEQI RMS TYPE
REMARK 500 PHE A 104 0.09 SIDE CHAIN
REMARK 500
REMARK 500 REMARK: NULL
DBREF 1J6Q A 30 161 UNP O52690 O52690_SHEPU 30 161
SEQADV 1J6Q PHE A 26 UNP O52690 CLONING ARTIFACT
SEQADV 1J6Q ALA A 27 UNP O52690 CLONING ARTIFACT
SEQADV 1J6Q ALA A 28 UNP O52690 CLONING ARTIFACT
SEQADV 1J6Q ASP A 29 UNP O52690 CLONING ARTIFACT
SEQRES 1 A 136 PHE ALA ALA ASP LEU ASN SER ASN LEU ASN LEU PHE TYR
SEQRES 2 A 136 THR PRO SER GLU ILE VAL ASN GLY LYS THR ASP THR GLY
SEQRES 3 A 136 VAL LYS PRO GLU ALA GLY GLN ARG ILE ARG VAL GLY GLY
SEQRES 4 A 136 MET VAL THR VAL GLY SER MET VAL ARG ASP PRO ASN SER
SEQRES 5 A 136 LEU HIS VAL GLN PHE ALA VAL HIS ASP SER LEU GLY GLY
SEQRES 6 A 136 GLU ILE LEU VAL THR TYR ASP ASP LEU LEU PRO ASP LEU
SEQRES 7 A 136 PHE ARG GLU GLY GLN GLY ILE VAL ALA GLN GLY VAL LEU
SEQRES 8 A 136 GLY GLU ASP GLY LYS LEU ALA ALA THR GLU VAL LEU ALA
SEQRES 9 A 136 LYS HIS ASP GLU ASN TYR MET PRO PRO GLU VAL ALA GLU
SEQRES 10 A 136 ALA MET GLY GLN LYS HIS GLU LYS LEU ASP TYR SER GLN
SEQRES 11 A 136 GLN LYS SER ALA THR GLN
SHEET 1 A 9 PHE A 37 TYR A 38 0
SHEET 2 A 9 ARG A 59 VAL A 66 1 O ARG A 61 N TYR A 38
SHEET 3 A 9 VAL A 80 HIS A 85 -1 N HIS A 85 O MET A 65
SHEET 4 A 9 VAL A 72 ARG A 73 -1 O VAL A 72 N GLN A 81
SHEET 5 A 9 VAL A 80 HIS A 85 -1 N GLN A 81 O VAL A 72
SHEET 6 A 9 ILE A 92 TYR A 96 -1 N ILE A 92 O VAL A 84
SHEET 7 A 9 LEU A 122 LEU A 128 1 O LEU A 122 N THR A 95
SHEET 8 A 9 GLY A 109 LEU A 116 -1 O VAL A 111 N LEU A 128
SHEET 9 A 9 ARG A 59 VAL A 66 -1 O ILE A 60 N GLY A 114
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
Complete list - 23 20 Bytes