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5ESD

Crystal Structure of M. tuberculosis MenD bound to ThDP and Mn2+

5ESD の概要
エントリーDOI10.2210/pdb5esd/pdb
関連するPDBエントリー5ERX 5ERY 5ESO 5ESS 5ESU
分子名称2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase, MANGANESE (II) ION, THIAMINE DIPHOSPHATE, ... (4 entities in total)
機能のキーワードmenaquinone biosynthesis, mend, 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexadiene-1-carboxylate synthase, thiamin-diphosphate dependent enzyme, pyruvate oxidase family, hydrolase
由来する生物種Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
タンパク質・核酸の鎖数4
化学式量合計242196.79
構造登録者
Johnston, J.M.,Jirgis, E.N.M.,Bashiri, G.,Bulloch, E.M.M.,Baker, E.N. (登録日: 2015-11-16, 公開日: 2016-06-22, 最終更新日: 2024-03-06)
主引用文献Jirgis, E.N.,Bashiri, G.,Bulloch, E.M.,Johnston, J.M.,Baker, E.N.
Structural Views along the Mycobacterium tuberculosis MenD Reaction Pathway Illuminate Key Aspects of Thiamin Diphosphate-Dependent Enzyme Mechanisms.
Structure, 24:1167-1177, 2016
Cited by
PubMed Abstract: Menaquinone (MQ) is an essential component of the respiratory chains of many pathogenic organisms, including Mycobacterium tuberculosis (Mtb). The first committed step in MQ biosynthesis is catalyzed by 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexadiene-1-carboxylate synthase (MenD), a thiamin diphosphate (ThDP)-dependent enzyme. Catalysis proceeds through two covalent intermediates as the substrates 2-oxoglutarate and isochorismate are successively added to the cofactor before final cleavage of the product. We have determined a series of crystal structures of Mtb-MenD that map the binding of both substrates, visualizing each step in the MenD catalytic cycle, including both intermediates. ThDP binding induces a marked asymmetry between the coupled active sites of each dimer, and possible mechanisms of communication can be identified. The crystal structures also reveal conformational features of the two intermediates that facilitate reaction but prevent premature product release. These data fully map chemical space to inform early-stage drug discovery targeting MenD.
PubMed: 27291649
DOI: 10.1016/j.str.2016.04.018
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.25 Å)
構造検証レポート
Validation report summary of 5esd
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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