Header list of 1w4h.pdb file
Complete list - r 25 2 Bytes
HEADER TRANSFERASE 23-JUL-04 1W4H
TITLE PERIPHERAL-SUBUNIT FROM MESOPHILIC, THERMOPHILIC AND
TITLE 2 HYPERTHERMOPHILIC BACTERIA FOLD BY ULTRAFAST, APPARENTLY
TITLE 3 TWO-STATE TRANSITIONS
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: DIHYDROLIPOYLLYSINE-RESIDUE ACETYLTRANSFERASE;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: RESIDUES 108-152;
COMPND 5 SYNONYM: DIHYDROLIPOAMIDE ACETYLTRANSFERASE;
COMPND 6 EC: 2.3.1.12;
COMPND 7 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: ESCHERICHIA COLI;
SOURCE 3 ORGANISM_TAXID: 562;
SOURCE 4 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE 5 EXPRESSION_SYSTEM_TAXID: 469008;
SOURCE 6 EXPRESSION_SYSTEM_STRAIN: BL21(DE3);
SOURCE 7 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 8 EXPRESSION_SYSTEM_PLASMID: PRSETA
KEYWDS ULTRAFAST FOLDING, HOMOLOGUES, PERIPHERAL-SUBUNIT BINDING
KEYWDS 2 DOMAINS, TRANSFERASE
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR N.FERGUSON,T.D.SHARPE,P.J.SCHARTAU,M.D.ALLEN,C.M.JOHNSON,
AUTHOR 2 A.R.FERSHT
REVDAT 4 24-FEB-09 1W4H 1 VERSN
REVDAT 3 20-DEC-06 1W4H 1 JRNL
REVDAT 2 02-SEP-05 1W4H 1 SOURCE
REVDAT 1 20-JUL-05 1W4H 0
JRNL AUTH N.FERGUSON,T.D.SHARPE,P.J.SCHARTAU,S.SATO,
JRNL AUTH 2 M.D.ALLEN,C.M.JOHNSON,T.J.RUTHERFORD,A.R.FERSHT
JRNL TITL ULTRA-FAST BARRIER-LIMITED FOLDING IN THE
JRNL TITL 2 PERIPHERAL SUBUNIT-BINDING DOMAIN FAMILY.
JRNL REF J.MOL.BIOL. V. 353 427 2005
JRNL REFN ISSN 0022-2836
JRNL PMID 16168437
JRNL DOI 10.1016/J.JMB.2005.08.031
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : CNS
REMARK 3 AUTHORS : BRUNGER,ADAMS,CLORE,DELANO,GROS, GROSSE-
REMARK 3 KUNSTLEVE,JIANG,KUSZEWSKI,NILGES, PANNU,READ,
REMARK 3 RICE,SIMONSON,WARREN
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: REFINEMENT DETAILS CAN BE FOUND IN
REMARK 3 THE JRNL CITATION ABOVE.
REMARK 4
REMARK 4 1W4H COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBE ON 26-JUL-04.
REMARK 100 THE PDBE ID CODE IS EBI-20571.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 298.0
REMARK 210 PH : 7.0
REMARK 210 IONIC STRENGTH : 200
REMARK 210 PRESSURE : 1.0
REMARK 210 SAMPLE CONTENTS : 95%WATER/5% D20,
REMARK 210 3MM SAMPLE
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : NULL
REMARK 210 SPECTROMETER FIELD STRENGTH : 800
REMARK 210 SPECTROMETER MODEL : DRX
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : ANSIG, AZARA, CNS
REMARK 210 METHOD USED : NULL
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 20
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 20
REMARK 210 CONFORMERS, SELECTION CRITERIA : NO VIOLATIONS > 0.25
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 1
REMARK 210
REMARK 210 REMARK: THE STRUCTURE WAS DETERMINED USING TRIPLE-RESONANCE
REMARK 210 NMR SPECTROSCOPY ON 13C,15N LABELLED MATERIAL
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 465
REMARK 465 MISSING RESIDUES
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE
REMARK 465 EXPERIMENT. (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 465 IDENTIFIER; SSSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)
REMARK 465
REMARK 465 M RES C SSSEQI
REMARK 465 GLY A 124
REMARK 465 SER A 125
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 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 2 ALA A 130 -46.12 -152.75
REMARK 500 2 LYS A 169 49.04 -90.58
REMARK 500 3 ALA A 168 42.01 -95.39
REMARK 500 5 ALA A 130 25.93 -148.74
REMARK 500 5 ALA A 168 35.11 -96.08
REMARK 500 6 ALA A 130 71.37 -167.02
REMARK 500 6 ALA A 168 33.74 -98.24
REMARK 500 7 ALA A 130 -39.96 -175.98
REMARK 500 7 ALA A 168 37.57 -95.60
REMARK 500 10 LYS A 169 39.49 32.27
REMARK 500 11 LYS A 169 85.41 61.89
REMARK 500 13 ASN A 143 29.39 49.89
REMARK 500 14 ALA A 168 30.71 -96.87
REMARK 500 15 LYS A 169 91.05 58.51
REMARK 500 16 ALA A 130 -65.37 69.67
REMARK 500 17 ALA A 168 43.17 -95.10
REMARK 500 18 ALA A 130 -39.65 -161.50
REMARK 500 19 ALA A 130 36.70 -142.91
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1B5S RELATED DB: PDB
REMARK 900 DIHYDROLIPOYL TRANSACETYLASE CATALYTIC DOMAIN
REMARK 900 (RESIDUES 184-425) FROM BACILLUS
REMARK 900 STEAROTHERMOPHILUS
REMARK 900 RELATED ID: 1EBD RELATED DB: PDB
REMARK 900 DIHYDROLIPOAMIDE DEHYDROGENASE COMPLEXED WITH
REMARK 900 THE BINDING DOMAIN OF THE DIHYDROLIPOAMIDE
REMARK 900 ACETYLASE
REMARK 900 RELATED ID: 1LAB RELATED DB: PDB
REMARK 900 DIHYDROLIPOAMIDE ACETYLTRANSFERASE (E2P) SUBUNIT
REMARK 900 OF THE PYRUVATE DEHYDROGENASE (PDH)
REMARK 900 MULTIENZYME COMPLEX (LIPOYLATED DOMAIN, RESIDUES
REMARK 900 1 - 80) (NMR, 11 STRUCTURES)
REMARK 900 RELATED ID: 1LAC RELATED DB: PDB
REMARK 900 DIHYDROLIPOAMIDE ACETYLTRANSFERASE (E2P) SUBUNIT
REMARK 900 OF THE PYRUVATE DEHYDROGENASE (PDH)
REMARK 900 MULTIENZYME COMPLEX (LIPOYLATED DOMAIN, RESIDUES
REMARK 900 1 - 80) (NMR, AVERAGE STRUCTURE)
REMARK 900 RELATED ID: 1W3D RELATED DB: PDB
REMARK 900 NMR STRUCTURE OF THE PERIPHERAL-SUBUNIT
REMARK 900 BINDING DOMAIN OF BACILLUS STEAROTHERMOPHILUS
REMARK 900 E2P
REMARK 900 RELATED ID: 2PDD RELATED DB: PDB
REMARK 900 DIHYDROLIPOAMIDE ACETYLTRANSFERASE (E2P) SUBUNIT
REMARK 900 OF THE PYRUVATE DEHYDROGENASE (PDH)
REMARK 900 MULTIENZYME COMPLEX (PYRUVATE DECARBOXYLASE (E1P)
REMARK 900 / DIHYDROLIPOAMIDE DEHYDROGENASE (E3) 43
REMARK 900 RESIDUE BINDING DOMAIN) (NMR, 35 STRUCTURES)
REMARK 900 RELATED ID: 2PDE RELATED DB: PDB
REMARK 900 DIHYDROLIPOAMIDE ACETYLTRANSFERASE (E2P) SUBUNIT
REMARK 900 OF THE PYRUVATE DEHYDROGENASE (PDH)
REMARK 900 MULTIENZYME COMPLEX (PYRUVATE DECARBOXYLASE (E1P)
REMARK 900 / DIHYDROLIPOAMIDE DEHYDROGENASE (E3) 43
REMARK 900 RESIDUE BINDING DOMAIN) (NMR, AVERAGE
REMARK 900 STRUCTURE)
REMARK 900 RELATED ID: 1W4E RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT FROM MESOPHILIC, THERMOPHILIC
REMARK 900 AND HYPERTHERMOPHILIC BACTERIA FOLD BY
REMARK 900 ULTRAFAST, APPARENTLY TWO-STATE TRANSITIONS
REMARK 900 RELATED ID: 1W4F RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT FROM MESOPHILIC, THERMOPHILIC
REMARK 900 AND HYPERTHERMOPHILIC BACTERIA FOLD BY
REMARK 900 ULTRAFAST, APPARENTLY TWO-STATE TRANSITIONS
REMARK 900 RELATED ID: 1W4G RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT FROM MESOPHILIC, THERMOPHILIC
REMARK 900 AND HYPERTHERMOPHILIC BACTERIA FOLD BY
REMARK 900 ULTRAFAST, APPARENTLY TWO-STATE TRANSITIONS
REMARK 900 RELATED ID: 1W4I RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT BINDING DOMAINS FROM
REMARK 900 MESOPHILIC, THERMOPHILIC, AND HYPERTHERMOPHILIC
REMARK 900 BACTERIA FOLD BY ULTRAFAST, APPARENTLY TWO-
REMARK 900 STATE TRANSITIONS
REMARK 900 RELATED ID: 1W4J RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT BINDING DOMAINS FROM
REMARK 900 MESOPHILIC, THERMOPHILIC, AND HYPERTHERMOPHILIC
REMARK 900 BACTERIA FOLD BY ULTRAFAST, APPARENTLY TWO-
REMARK 900 STATE TRANSITIONS
REMARK 900 RELATED ID: 1W4K RELATED DB: PDB
REMARK 900 PERIPHERAL-SUBUNIT BINDING DOMAINS FROM
REMARK 900 MESOPHILIC, THERMOPHILIC, AND HYPERTHERMOPHILIC
REMARK 900 BACTERIA FOLD BY ULTRAFAST, APPARENTLY TWO-
REMARK 900 STATE TRANSITIONS
DBREF 1W4H A 124 125 PDB 1W4H 1W4H 124 125
DBREF 1W4H A 126 170 UNP P11961 ODP2_BACST 108 152
SEQRES 1 A 47 GLY SER GLN ASN ASN ASP ALA LEU SER PRO ALA ILE ARG
SEQRES 2 A 47 ARG LEU LEU ALA GLU HIS ASN LEU ASP ALA SER ALA ILE
SEQRES 3 A 47 LYS GLY THR GLY VAL GLY GLY ARG LEU THR ARG GLU ASP
SEQRES 4 A 47 VAL GLU LYS HIS LEU ALA LYS ALA
HELIX 1 1 SER A 132 HIS A 142 1 11
HELIX 2 2 ASP A 145 ILE A 149 5 5
HELIX 3 3 THR A 159 ALA A 170 1 12
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 25 2 Bytes