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Open data
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Basic information
Entry | Database: PDB / ID: 1hvw | ||||||
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Title | HAIRPINLESS MUTANT OF OMEGA-ATRACOTOXIN-HV1A | ||||||
![]() | OMEGA-ATRACOTOXIN-HV1A | ||||||
![]() | TOXIN / cystine knot / beta-hairpin | ||||||
Function / homology | Omega-atracotoxin / Omega-atracotoxin, conserved site / Omega-atracotoxin / Omega-atracotoxin (ACTX) type 1 family signature. / calcium channel inhibitor activity / defense response / toxin activity / extracellular region / Omega-hexatoxin-Hv1a![]() | ||||||
Method | SOLUTION NMR / Torsion angle dynamics, dynamical simulated annealing | ||||||
![]() | Fletcher, J.I. / King, G.F. | ||||||
![]() | ![]() Title: Functional significance of the beta hairpin in the insecticidal neurotoxin omega-atracotoxin-Hv1a. Authors: Tedford, H.W. / Fletcher, J.I. / King, G.F. #1: ![]() Title: The Structure of a Novel Insecticidal Neurotoxin, Omega-Atracotoxin-HV1, from the Venom of an Australian Funnel Web Spider Authors: Fletcher, J.I. / Smith, R. / O'Donoghue, S.I. / Nilges, M. / Connor, M. / Howden, M.E. / Christie, M.J. / King, G.F. #2: ![]() Title: Structure-function Studies of Omega-atracotoxin, A Potent Antagonist of Insect Voltage-gated Calcium Channels Authors: Wang, X. / Smith, R. / Fletcher, J.I. / Wilson, H. / Wood, C.J. / Howden, M.E. / King, G.F. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 111.9 KB | Display | ![]() |
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PDB format | ![]() | 88.1 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 333 KB | Display | ![]() |
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Full document | ![]() | 413.9 KB | Display | |
Data in XML | ![]() | 7.8 KB | Display | |
Data in CIF | ![]() | 12.8 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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NMR ensembles |
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Components
#1: Protein/peptide | Mass: 2623.899 Da / Num. of mol.: 1 / Source method: obtained synthetically Details: This peptide was chemically synthesized. The native peptide is naturally found in Hadronyche versuta (Blue mountain funnel-web spider).The mutant hairpinless toxin was synthesized by solid- ...Details: This peptide was chemically synthesized. The native peptide is naturally found in Hadronyche versuta (Blue mountain funnel-web spider).The mutant hairpinless toxin was synthesized by solid-phase peptide synthesis, oxidized/folded in a glutathione redox buffer, then purified using reverse-phase HPLC. References: UniProt: P56207 |
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-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR | ||||||||||||||||||||||||||||
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NMR experiment |
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NMR details | Text: This structure was determined using standard 2D homonuclear techniques. |
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Sample preparation
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Sample conditions | Ionic strength: 0.005 / pH: 4.9 / Pressure: 1 atm / Temperature: 298 K | |||||||||
Crystal grow | *PLUS Method: other / Details: NMR |
-NMR measurement
NMR spectrometer | Type: Bruker DRX / Manufacturer: Bruker / Model: DRX / Field strength: 600 MHz |
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Processing
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Refinement | Method: Torsion angle dynamics, dynamical simulated annealing Software ordinal: 1 Details: The structures are based on a total of 231 NOE-derived distance restraints, 19 dihedral-angle restraints, and 16 restraints defining 8 hydrogen bonds. | ||||||||||||||||||||
NMR representative | Selection criteria: lowest energy | ||||||||||||||||||||
NMR ensemble | Conformer selection criteria: structures with the lowest energy Conformers calculated total number: 100 / Conformers submitted total number: 20 |