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5DOZ

Crystal structure of JamJ enoyl reductase (NADPH bound)

5DOZ の概要
エントリーDOI10.2210/pdb5doz/pdb
関連するPDBエントリー5DOV 5DP1 5DP2
分子名称JamJ, ACETATE ION, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (4 entities in total)
機能のキーワードenoyl reductase, polyketide synthase, nadph, cyclopropane, oxidoreductase
由来する生物種Lyngbya majuscula
タンパク質・核酸の鎖数3
化学式量合計116035.64
構造登録者
Khare, D.,Smith, J.L. (登録日: 2015-09-11, 公開日: 2015-11-18, 最終更新日: 2023-09-27)
主引用文献Khare, D.,Hale, W.A.,Tripathi, A.,Gu, L.,Sherman, D.H.,Gerwick, W.H.,Hakansson, K.,Smith, J.L.
Structural Basis for Cyclopropanation by a Unique Enoyl-Acyl Carrier Protein Reductase.
Structure, 23:2213-2223, 2015
Cited by
PubMed Abstract: The natural product curacin A, a potent anticancer agent, contains a rare cyclopropane group. The five enzymes for cyclopropane biosynthesis are highly similar to enzymes that generate a vinyl chloride moiety in the jamaicamide natural product. The structural biology of this remarkable catalytic adaptability is probed with high-resolution crystal structures of the curacin cyclopropanase (CurF ER), an in vitro enoyl reductase (JamJ ER), and a canonical curacin enoyl reductase (CurK ER). The JamJ and CurK ERs catalyze NADPH-dependent double bond reductions typical of enoyl reductases (ERs) of the medium-chain dehydrogenase reductase (MDR) superfamily. Cyclopropane formation by CurF ER is specified by a short loop which, when transplanted to JamJ ER, confers cyclopropanase activity on the chimeric enzyme. Detection of an adduct of NADPH with the model substrate crotonyl-CoA provides indirect support for a recent proposal of a C2-ene intermediate on the reaction pathway of MDR enoyl-thioester reductases.
PubMed: 26526850
DOI: 10.1016/j.str.2015.09.013
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.26 Å)
構造検証レポート
Validation report summary of 5doz
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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