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1KQH

NMR Solution Structure of the cis Pro30 Isomer of ACTX-Hi:OB4219

1KQH の概要
エントリーDOI10.2210/pdb1kqh/pdb
関連するPDBエントリー1KQI
分子名称ACTX-Hi:OB4219 (1 entity in total)
機能のキーワードhadronyche infensa, funnel web, spider venom, cis-trans isomerisation, disulfide rich, cystine knot, solution structure, nmr spectroscopy, toxin
由来する生物種Hadronyche infensa
タンパク質・核酸の鎖数1
化学式量合計4230.95
構造登録者
Rosengren, K.J.,Wilson, D.,Daly, N.L.,Alewood, P.F.,Craik, D.J. (登録日: 2002-01-05, 公開日: 2002-02-06, 最終更新日: 2024-10-30)
主引用文献Rosengren, K.J.,Wilson, D.,Daly, N.L.,Alewood, P.F.,Craik, D.J.
Solution structures of the cis- and trans-Pro30 isomers of a novel 38-residue toxin from the venom of Hadronyche Infensa sp. that contains a cystine-knot motif within its four disulfide bonds
Biochemistry, 41:3294-3301, 2002
Cited by
PubMed Abstract: The primary sequence and three-dimensional structure of a novel peptide toxin isolated from the Australian funnel-web spider Hadronyche infensa sp. is reported. ACTX-Hi:OB4219 contains 38 amino acids, including eight-cysteine residues that form four disulfide bonds. The connectivities of these disulfide bonds were previously unknown but have been unambiguously determined in this study. Three of these disulfide bonds are arranged in an inhibitor cystine-knot (ICK) motif, which is observed in a range of other disulfide-rich peptide toxins. The motif incorporates an embedded ring in the structure formed by two of the disulfides and their connecting backbone segments penetrated by a third disulfide bond. Using NMR spectroscopy, we determined that despite the isolation of a single native homologous product by RP-HPLC, ACTX-Hi:OB4219 possesses two equally populated conformers in solution. These two conformers were determined to arise from cis/trans isomerization of the bond preceding Pro30. Full assignment of the NMR spectra for both conformers allowed for the calculation of their structures, revealing the presence of a triple-stranded antiparallel beta sheet consistent with the inhibitor cystine-knot (ICK) motif.
PubMed: 11876637
DOI: 10.1021/bi011932y
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 1kqh
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件を2025-12-03に公開中

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