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1CHP

SURPRISING LEADS FOR A CHOLERA TOXIN RECEPTOR BINDING ANTAGONIST; CRYSTALLOGRAPHIC STUDIES OF CTB MUTANTS

1CHP の概要
エントリーDOI10.2210/pdb1chp/pdb
分子名称CHOLERA TOXIN B PENTAMER, CHLORIDE ION (3 entities in total)
機能のキーワードtoxin
由来する生物種Vibrio cholerae
タンパク質・核酸の鎖数5
化学式量合計58441.97
構造登録者
Merritt, E.A.,Hol, W.G.J. (登録日: 1995-02-15, 公開日: 1996-03-08, 最終更新日: 2024-11-20)
主引用文献Merritt, E.A.,Sarfaty, S.,Chang, T.T.,Palmer, L.M.,Jobling, M.G.,Holmes, R.K.,Hol, W.G.
Surprising leads for a cholera toxin receptor-binding antagonist: crystallographic studies of CTB mutants.
Structure, 3:561-570, 1995
Cited by
PubMed Abstract: Because agents which inhibit the receptor binding of cholera toxin constitute possible lead compounds for the structure-based design of anti-cholera drugs, detailed investigation of the toxin's receptor-binding site is of key importance. The substitution Gly-->Asp at residue 33 of the cholera toxin B subunit (CTB) has been reported to abolish receptor-binding ability. The substitution Arg35-->Asp has been reported to result in deficient assembly of the AB5 holotoxin. The molecular basis for these effects was not readily apparent from analysis of an earlier crystal structure of the wild-type toxin B pentamer in a complex with the receptor pentasaccharide.
PubMed: 8590017
DOI: 10.1016/S0969-2126(01)00190-3
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 1chp
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2025-12-31に公開中

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