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4PH6

Structure of 3-Dehydroquinate Dehydratase from Enterococcus faecalis

4PH6 の概要
エントリーDOI10.2210/pdb4ph6/pdb
分子名称3-dehydroquinate dehydratase (2 entities in total)
機能のキーワード(beta/alpha)8 barrel, lyase
由来する生物種Enterococcus faecalis
タンパク質・核酸の鎖数2
化学式量合計56789.27
構造登録者
Xue, B.,Cheung, V.W.,Yew, W.S.,Robinson, R.C. (登録日: 2014-05-05, 公開日: 2014-09-17, 最終更新日: 2023-11-08)
主引用文献Cheung, V.W.,Xue, B.,Hernandez-Valladares, M.,Go, M.K.,Tung, A.,Aguda, A.H.,Robinson, R.C.,Yew, W.S.
Identification of Polyketide Inhibitors Targeting 3-Dehydroquinate Dehydratase in the Shikimate Pathway of Enterococcus faecalis
Plos One, 9:e103598-e103598, 2014
Cited by
PubMed Abstract: Due to the emergence of resistance toward current antibiotics, there is a pressing need to develop the next generation of antibiotics as therapeutics against infectious and opportunistic diseases of microbial origins. The shikimate pathway is exclusive to microbes, plants and fungi, and hence is an attractive and logical target for development of antimicrobial therapeutics. The Gram-positive commensal microbe, Enterococcus faecalis, is a major human pathogen associated with nosocomial infections and resistance to vancomycin, the "drug of last resort". Here, we report the identification of several polyketide-based inhibitors against the E. faecalis shikimate pathway enzyme, 3-dehydroquinate dehydratase (DHQase). In particular, marein, a flavonoid polyketide, both inhibited DHQase and retarded the growth of Enterococcus faecalis. The purification, crystallization and structural resolution of recombinant DHQase from E. faecalis (at 2.2 Å resolution) are also reported. This study provides a route in the development of polyketide-based antimicrobial inhibitors targeting the shikimate pathway of the human pathogen E. faecalis.
PubMed: 25072253
DOI: 10.1371/journal.pone.0103598
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 4ph6
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2025-06-18に公開中

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