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2RJS

SgTAM bound to substrate mimic

2RJS の概要
エントリーDOI10.2210/pdb2rjs/pdb
関連するPDBエントリー2OHY 2QVE 2RJR
分子名称Tyrosine aminomutase, (3R)-3-amino-2,2-difluoro-3-(4-methoxyphenyl)propanoic acid (3 entities in total)
機能のキーワード4-methylidene imidazole, mio, aminomutase, c-1027, isomerase
由来する生物種Streptomyces globisporus
タンパク質・核酸の鎖数2
化学式量合計116799.92
構造登録者
Montavon, T.J.,Christianson, C.V.,Bruner, S.D. (登録日: 2007-10-15, 公開日: 2008-01-15, 最終更新日: 2026-03-18)
主引用文献Montavon, T.J.,Christianson, C.V.,Festin, G.M.,Shen, B.,Bruner, S.D.
Design and characterization of mechanism-based inhibitors for the tyrosine aminomutase SgTAM.
Bioorg.Med.Chem.Lett., 18:3099-3102, 2008
Cited by
PubMed Abstract: The synthesis and evaluation of two classes of inhibitors for SgTAM, a 4-methylideneimidazole-5-one (MIO) containing tyrosine aminomutase, are described. A mechanism-based strategy was used to design analogs that mimic the substrate or product of the reaction and form covalent interactions with the enzyme through the MIO prosthetic group. The analogs were characterized by measuring inhibition constants and X-ray crystallographic structural analysis of the co-complexes bound to the aminomutase, SgTAM.
PubMed: 18078753
DOI: 10.1016/j.bmcl.2007.11.046
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4 Å)
構造検証レポート
Validation report summary of 2rjs
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2026-04-15に公開中

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