Header list of 1hp3.pdb file
Complete list - 23 20 Bytes
HEADER TOXIN 12-DEC-00 1HP3
TITLE C-TERMINAL TRUNCATION OF OMEGA-ATRACOTOXIN-HV2A (CT-HV2A)
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: OMEGA-ATRACOTOXIN-HV2A;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: N-TERMINAL (RESIDUES 1-32);
COMPND 5 SYNONYM: CT-HV2A;
COMPND 6 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 SYNTHETIC: YES;
SOURCE 3 OTHER_DETAILS: THIS SEQUENCE DOES NOT OCCUR NATURALLY. THE PEPTIDE
SOURCE 4 WAS CHEMICALLY SYNTHESIZED USING STANDARD T-BOC CHEMISTRY, AND
SOURCE 5 OXIDIZED/FOLDED IN A GLUTATHIONE REDOX BUFFER.
KEYWDS CYSTINE KNOT, TOXIN
EXPDTA SOLUTION NMR
NUMMDL 20
AUTHOR X.-H.WANG,G.F.KING
REVDAT 3 23-FEB-22 1HP3 1 REMARK
REVDAT 2 24-FEB-09 1HP3 1 VERSN
REVDAT 1 11-DEC-02 1HP3 0
JRNL AUTH X.-H.WANG,M.CONNOR,D.WILSON,H.I.WILSON,G.M.NICHOLSON,
JRNL AUTH 2 R.SMITH,D.SHAW,J.P.MACKAY,P.F.ALEWOOD,M.J.CHRISTIE,G.F.KING
JRNL TITL DISCOVERY AND STRUCTURE OF A POTENT AND HIGHLY SPECIFIC
JRNL TITL 2 BLOCKER OF INSECT CALCIUM CHANNELS
JRNL REF J.BIOL.CHEM. V. 276 40306 2001
JRNL REFN ISSN 0021-9258
JRNL PMID 11522785
REMARK 1
REMARK 1 REFERENCE 1
REMARK 1 AUTH X.-H.WANG,M.CONNOR,R.SMITH,M.W.MACIEJEWSKI,M.E.H.HOWDEN,
REMARK 1 AUTH 2 G.M.NICHOLSON
REMARK 1 TITL DISCOVERY AND CHARACTERIZATION OF A FAMILY OF INSECTICIDAL
REMARK 1 TITL 2 NEUROTOXINS WITH A RARE VICINAL DISULFIDE BRIDGE.
REMARK 1 REF NAT.STRUCT.BIOL. V. 7 505 2000
REMARK 1 REFN ISSN 1072-8368
REMARK 1 DOI 10.1038/75921
REMARK 1 REFERENCE 2
REMARK 1 AUTH J.I.FLETCHER,R.SMITH,S.I.O'DONOGHUE,M.NILGES,M.CONNOR,
REMARK 1 AUTH 2 M.E.HOWDEN,M.J.CHRISTIE,G.F.KING
REMARK 1 TITL THE STRUCTURE OF A NOVEL INSECTICIDAL NEUROTOXIN,
REMARK 1 TITL 2 OMEGA-ATRACOTOXIN-HV1, FROM THE VENOM OF AN AUSTRALIAN
REMARK 1 TITL 3 FUNNEL WEB SPIDER.
REMARK 1 REF NAT.STRUCT.BIOL. V. 4 559 1997
REMARK 1 REFN ISSN 1072-8368
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : VNMR 6.1B, X-PLOR 3.1
REMARK 3 AUTHORS : VARIAN (VNMR), AXEL BRUNGER (X-PLOR)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: THE STRUCTURES ARE BASED ON A TOTAL OF
REMARK 3 345 NOE-DERIVED DISTANCE RESTRAINTS, 21 DIHEDRAL-ANGLE
REMARK 3 RESTRAINTS, PLUS 22 RESTRAINTS DEFINING 11 HYDROGEN BONDS.
REMARK 4
REMARK 4 1HP3 COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 14-DEC-00.
REMARK 100 THE DEPOSITION ID IS D_1000012494.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 296
REMARK 210 PH : 4.71
REMARK 210 IONIC STRENGTH : 0.005
REMARK 210 PRESSURE : 1 ATM
REMARK 210 SAMPLE CONTENTS : 2.5 MM CT-HV2A; 2.5 MM CT-HV2A
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 2D_TOCSY; 2D_NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 600 MHZ
REMARK 210 SPECTROMETER MODEL : INOVA
REMARK 210 SPECTROMETER MANUFACTURER : VARIAN
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : FELIX FELIX97, X-EASY 1.3.13,
REMARK 210 DYANA 1.5
REMARK 210 METHOD USED : TORSION ANGLE DYNAMICS FOLLOWED
REMARK 210 BY DYNAMICAL 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: THIS STRUCTURE WAS DETERMINED USING STANDARD 2D
REMARK 210 HOMONUCLEAR NMR TECHNIQUES.
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 ALA A 3 64.28 -114.95
REMARK 500 1 CYS A 4 96.32 -176.02
REMARK 500 1 PHE A 6 -75.20 -128.23
REMARK 500 1 SER A 13 164.53 179.53
REMARK 500 1 SER A 31 47.26 -93.21
REMARK 500 2 LEU A 2 -159.06 -97.02
REMARK 500 2 CYS A 4 95.32 -177.14
REMARK 500 2 PHE A 6 -76.16 -129.58
REMARK 500 2 SER A 13 165.18 179.69
REMARK 500 2 SER A 31 46.41 -93.17
REMARK 500 3 ALA A 3 36.59 -176.41
REMARK 500 3 CYS A 4 97.65 -178.79
REMARK 500 3 PHE A 6 -71.20 -132.66
REMARK 500 3 SER A 31 32.91 -96.02
REMARK 500 4 ALA A 3 40.94 -147.56
REMARK 500 4 CYS A 4 97.02 -177.58
REMARK 500 4 PHE A 6 -77.20 -123.60
REMARK 500 4 SER A 13 166.55 179.12
REMARK 500 4 SER A 31 47.02 -92.78
REMARK 500 5 CYS A 4 95.96 -177.40
REMARK 500 5 PHE A 6 -75.78 -125.03
REMARK 500 6 ALA A 3 41.60 -104.26
REMARK 500 6 CYS A 4 96.36 -177.29
REMARK 500 6 PHE A 6 -76.46 -127.99
REMARK 500 6 SER A 13 166.59 179.60
REMARK 500 6 SER A 31 47.60 -93.14
REMARK 500 7 CYS A 4 97.81 -177.95
REMARK 500 7 PHE A 6 -77.24 -121.89
REMARK 500 7 SER A 13 167.36 179.16
REMARK 500 7 SER A 31 47.14 -92.96
REMARK 500 8 LEU A 2 85.30 -175.71
REMARK 500 8 ALA A 3 34.12 -163.35
REMARK 500 8 CYS A 4 96.57 -177.61
REMARK 500 8 PHE A 6 -77.39 -123.46
REMARK 500 8 SER A 13 166.15 179.69
REMARK 500 8 SER A 31 47.41 -93.33
REMARK 500 9 CYS A 4 94.85 -177.03
REMARK 500 9 PHE A 6 -77.28 -130.56
REMARK 500 9 SER A 31 47.05 -93.03
REMARK 500 10 LEU A 2 40.90 -104.20
REMARK 500 10 ALA A 3 33.46 -144.76
REMARK 500 10 CYS A 4 95.37 -177.11
REMARK 500 10 PHE A 6 -78.13 -127.86
REMARK 500 10 SER A 31 31.54 -95.96
REMARK 500 11 ALA A 3 39.13 -158.60
REMARK 500 11 CYS A 4 98.20 -178.06
REMARK 500 11 PHE A 6 -80.91 -125.77
REMARK 500 11 SER A 13 164.00 179.88
REMARK 500 11 SER A 31 47.54 -93.33
REMARK 500 12 LEU A 2 -160.91 -118.67
REMARK 500
REMARK 500 THIS ENTRY HAS 91 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1G9P RELATED DB: PDB
REMARK 900 FULL-LENGTH OMEGA-ATRACOTOXIN-HV2A
DBREF 1HP3 A 1 32 UNP P82852 TOT2A_HADVE 1 32
SEQRES 1 A 32 LEU LEU ALA CYS LEU PHE GLY ASN GLY ARG CYS SER SER
SEQRES 2 A 32 ASN ARG ASP CYS CYS GLU LEU THR PRO VAL CYS LYS ARG
SEQRES 3 A 32 GLY SER CYS VAL SER SER
HELIX 1 1 SER A 13 CYS A 17 5 5
SHEET 1 A 2 VAL A 23 LYS A 25 0
SHEET 2 A 2 SER A 28 VAL A 30 -1 O SER A 28 N LYS A 25
SSBOND 1 CYS A 4 CYS A 18 1555 1555 2.02
SSBOND 2 CYS A 11 CYS A 24 1555 1555 2.02
SSBOND 3 CYS A 17 CYS A 29 1555 1555 2.02
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 - 23 20 Bytes