Header list of 2gdx.pdb file
Complete list - v 10 2 Bytes
HEADER LIGASE/TRANSPORT PROTEIN 17-MAR-06 2GDX
TITLE SOLUTION STRUCTURE OF THE B. BREVIS TYCC3-PCP IN H-STATE
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: TYROCIDINE SYNTHETASE III;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: ACYL CARRIER 3, TYCC3 THIOESTER DOMAIN;
COMPND 5 SYNONYM: NON-RIBOSOMAL PEPTIDE SYNTHETASE PEPTIDYL CARRIER PROTEIN;
COMPND 6 ENGINEERED: YES;
COMPND 7 MUTATION: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: BREVIBACILLUS PARABREVIS;
SOURCE 3 ORGANISM_TAXID: 54914;
SOURCE 4 STRAIN: ATCC8185;
SOURCE 5 GENE: TYCC;
SOURCE 6 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE 7 EXPRESSION_SYSTEM_TAXID: 562;
SOURCE 8 EXPRESSION_SYSTEM_STRAIN: XL10;
SOURCE 9 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 10 EXPRESSION_SYSTEM_PLASMID: PQE70
KEYWDS THREE-HELIX BUNDLE, LIGASE-TRANSPORT PROTEIN COMPLEX
EXPDTA SOLUTION NMR
NUMMDL 16
AUTHOR A.KOGLIN,F.LOEHR,V.V.ROGOV,M.A.MARAHIEL,F.BERNHARD,V.DOETSCH
REVDAT 3 10-NOV-21 2GDX 1 REMARK SEQADV
REVDAT 2 24-FEB-09 2GDX 1 VERSN
REVDAT 1 01-AUG-06 2GDX 0
JRNL AUTH A.KOGLIN,M.R.MOFID,F.LOEHR,B.SCHAEFER,V.V.ROGOV,M.-M.BLUM,
JRNL AUTH 2 T.MITTAG,M.A.MARAHIEL,F.BERNHARD,V.DOETSCH
JRNL TITL CONFORMATIONAL SWITCHES MODULATE PROTEIN INTERACTIONS IN
JRNL TITL 2 PEPTIDE ANTIBIOTIC SYNTHETASES
JRNL REF SCIENCE V. 312 273 2006
JRNL REFN ISSN 0036-8075
JRNL PMID 16614225
JRNL DOI 10.1126/SCIENCE.1122928
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),
REMARK 3 BRUNGER,ADAMS,CLORE,DELANO,GROS,GROSSE-KUNSTLEVE,JIANG,KUSZEWSKI,
REMARK 3 NILGES, PANNU,READ,RICE,SIMONSON,WARREN (CNS)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 2GDX COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 22-MAR-06.
REMARK 100 THE DEPOSITION ID IS D_1000036998.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 298
REMARK 210 PH : 6.8
REMARK 210 IONIC STRENGTH : 50MM NAPI
REMARK 210 PRESSURE : 1 ATM
REMARK 210 SAMPLE CONTENTS : 0.8MM A/H-PCP U-15N; 50MM NAPI;
REMARK 210 1MM TCEP; 95% H2O; 5% D2O; 0.8MM
REMARK 210 A/H-PCP; 50MM NAPI; 100% D2O
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_15N-SEPARATED_NOESY; 2D NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 900 MHZ; 800 MHZ
REMARK 210 SPECTROMETER MODEL : AVANCE
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : XWINNMR 2.6, SPARKY 3.111, CYANA
REMARK 210 2.1
REMARK 210 METHOD USED : ENERGY MINIMIZATION
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 100
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 16
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: CLOSE CONTACTS
REMARK 500
REMARK 500 THE FOLLOWING ATOMS ARE IN CLOSE CONTACT.
REMARK 500
REMARK 500 ATM1 RES C SSEQI ATM2 RES C SSEQI DISTANCE
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 1 VAL A 29 12.71 59.09
REMARK 500 1 SER A 30 -68.62 -98.46
REMARK 500 1 ILE A 34 49.45 -103.28
REMARK 500 1 ASP A 36 150.78 66.13
REMARK 500 1 ASN A 37 -96.21 -177.76
REMARK 500 1 PHE A 39 -83.89 -78.67
REMARK 500 1 ILE A 41 -36.52 -172.03
REMARK 500 1 SER A 45 -145.25 31.16
REMARK 500 1 LEU A 46 31.57 -146.92
REMARK 500 1 TYR A 59 88.26 57.74
REMARK 500 1 VAL A 61 -72.71 65.86
REMARK 500 1 GLU A 62 -84.44 -92.81
REMARK 500 1 LYS A 66 83.45 47.15
REMARK 500 1 VAL A 67 -44.30 -155.62
REMARK 500 1 LEU A 68 -39.53 -178.27
REMARK 500 1 GLN A 71 115.27 176.42
REMARK 500 1 PRO A 72 41.35 -75.99
REMARK 500 1 THR A 73 74.54 -157.91
REMARK 500 1 TYR A 80 -69.95 -129.91
REMARK 500 1 ARG A 84 -83.89 58.40
REMARK 500 2 THR A 4 -124.86 60.20
REMARK 500 2 GLU A 5 165.25 66.39
REMARK 500 2 ILE A 34 -79.91 66.27
REMARK 500 2 ASP A 36 -92.73 41.75
REMARK 500 2 ASN A 37 -7.39 92.74
REMARK 500 2 PHE A 39 -73.13 -91.75
REMARK 500 2 ILE A 41 -18.42 168.69
REMARK 500 2 HIS A 56 40.89 -91.68
REMARK 500 2 ARG A 57 -150.81 177.81
REMARK 500 2 VAL A 61 -96.39 58.82
REMARK 500 2 PRO A 72 1.19 -68.49
REMARK 500 2 TYR A 80 -88.89 -114.04
REMARK 500 2 THR A 83 -55.95 -141.69
REMARK 500 3 ALA A 10 74.98 -164.06
REMARK 500 3 PRO A 11 -133.69 -81.61
REMARK 500 3 LEU A 27 -81.13 -93.04
REMARK 500 3 VAL A 29 53.06 70.18
REMARK 500 3 ILE A 32 -80.79 -87.69
REMARK 500 3 ASN A 37 -8.12 -140.85
REMARK 500 3 PHE A 38 -33.81 -148.34
REMARK 500 3 PHE A 39 -83.09 -96.53
REMARK 500 3 LEU A 46 45.68 -89.15
REMARK 500 3 ARG A 57 -63.90 -106.25
REMARK 500 3 GLU A 58 -151.97 -167.30
REMARK 500 3 LEU A 68 -51.23 -176.61
REMARK 500 3 GLN A 71 123.57 167.06
REMARK 500 3 THR A 73 39.75 -87.47
REMARK 500 3 ALA A 82 30.32 -150.96
REMARK 500 4 GLU A 5 -146.33 56.42
REMARK 500 4 ALA A 6 83.96 -152.91
REMARK 500
REMARK 500 THIS ENTRY HAS 277 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 2GDW RELATED DB: PDB
REMARK 900 SOLUTION STRUCTURE OF THE B. BREVIS TYCC3-PCP IN A/H-STATE
REMARK 900 RELATED ID: 2GDY RELATED DB: PDB
REMARK 900 SOLUTION STRUCTURE OF THE B. BREVIS TYCC3-PCP IN A-STATE
REMARK 900 RELATED ID: 2GE1 RELATED DB: PDB
REMARK 900 PROTEIN COMPLEX OF A-STATE TYCC3-APO-PCP WITH THE PPTASE SFP (MODEL)
REMARK 900 RELATED ID: 2GE0 RELATED DB: PDB
REMARK 900 ACTIVE COMPLEX OF COENZYME A WITH THE PPTASE SFP (MODEL)
DBREF 2GDX A 2 83 UNP O30409 TYCC_BREPA 3032 3113
SEQADV 2GDX MET A 1 UNP O30409 INITIATING METHIONINE
SEQADV 2GDX GLY A 2 UNP O30409 PRO 3032 ENGINEERED MUTATION
SEQADV 2GDX ARG A 84 UNP O30409 CLONING ARTIFACT
SEQADV 2GDX SER A 85 UNP O30409 CLONING ARTIFACT
SEQRES 1 A 85 MET GLY VAL THR GLU ALA GLN TYR VAL ALA PRO THR ASN
SEQRES 2 A 85 ALA VAL GLU SER LYS LEU ALA GLU ILE TRP GLU ARG VAL
SEQRES 3 A 85 LEU GLY VAL SER GLY ILE GLY ILE LEU ASP ASN PHE PHE
SEQRES 4 A 85 GLN ILE GLY GLY HIS SER LEU LYS ALA MET ALA VAL ALA
SEQRES 5 A 85 ALA GLN VAL HIS ARG GLU TYR GLN VAL GLU LEU PRO LEU
SEQRES 6 A 85 LYS VAL LEU PHE ALA GLN PRO THR ILE LYS ALA LEU ALA
SEQRES 7 A 85 GLN TYR VAL ALA THR ARG SER
HELIX 1 1 ASN A 13 LEU A 27 1 15
HELIX 2 2 LYS A 47 HIS A 56 1 10
HELIX 3 3 THR A 73 GLN A 79 1 7
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 - v 10 2 Bytes