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1B7D

NEUROTOXIN (TS1) FROM BRAZILIAN SCORPION TITYUS SERRULATUS

1B7D の概要
エントリーDOI10.2210/pdb1b7d/pdb
分子名称PROTEIN (NEUROTOXIN TS1), PHOSPHATE ION (3 entities in total)
機能のキーワードlong-chain neurotoxin, toxin
由来する生物種Tityus serrulatus (Brazilian scorpion)
タンパク質・核酸の鎖数1
化学式量合計6995.98
構造登録者
Polikarpov, I.,Sanches Jr., M.S.,Marangoni, S.,Toyama, M.H.,Teplyakov, A. (登録日: 1999-01-21, 公開日: 1999-07-22, 最終更新日: 2024-11-06)
主引用文献Polikarpov, I.,Junior, M.S.,Marangoni, S.,Toyama, M.H.,Teplyakov, A.
Crystal structure of neurotoxin Ts1 from Tityus serrulatus provides insights into the specificity and toxicity of scorpion toxins.
J.Mol.Biol., 290:175-184, 1999
Cited by
PubMed Abstract: The crystal structure of neurotoxin Ts1, a major component of the venom of the Brazilian scorpion Tityus serrulatus, has been determined at 1.7 A resolution. It is the first X-ray structure of a highly toxic anti-mammalian beta-toxin. The folding of the polypeptide chain of Ts1 is similar to that of other scorpion toxins. A cysteine-stabilised alpha-helix/beta-sheet motif forms the core of the flattened molecule. All residues identified as functionally important by chemical modification and site-directed mutagenesis are located on one side of the molecule, which is therefore considered as the Na+channel recognition site. The distribution of charged and non-polar residues over this surface determines the specificity of the toxin-channel interaction. Comparison to other scorpion toxins shows that positively charged groups at positions 1 and 12 as well as a negative charge at position 2 are likely determinants of the specificity of beta-toxins. In contrast, the contribution of the conserved aromatic cluster to the interaction might be relatively small. Comparison of Ts1 to weak beta-toxins from Centruroides sculpturatus Ewing reveals that a number of basic amino acid residues located on the face of the molecule opposite to the binding surface may account for the high toxicity of Ts1.
PubMed: 10388565
DOI: 10.1006/jmbi.1999.2868
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.73 Å)
構造検証レポート
Validation report summary of 1b7d
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-08-26に公開中

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