6O0N

M.tb MenD with Inhibitor

6O0N の概要

• エントリーDOI: 10.2210/pdb6o0n/pdb
• 関連するPDBエントリー: 5ERX 5ERY 5ESD 5ESO 5ESS 5ESU 6O04 6O0G 6O0J
• 分子名称: 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase, 1,4-dihydroxy-2-naphthoic acid (3 entities in total)
• 機能のキーワード: menaquinone biosynthesis, thdp dependent, decarboxylation, c-c bond ligation, inhibitor complex, sephchc synthase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 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: 241092.50

構造登録者

Johnston, J.M.,Ho, N.A.T.,Bashiri, G.,Bulloch, E.M.,Nigon, L.V.,Jirgis, E.M.N.,Baker, E.N. (登録日: 2019-02-16, 公開日: 2020-02-19, 最終更新日: 2023-10-11)

主引用文献

Bashiri, G.,Nigon, L.V.,Jirgis, E.N.M.,Ho, N.A.T.,Stanborough, T.,Dawes, S.S.,Baker, E.N.,Bulloch, E.M.M.,Johnston, J.M.
Allosteric regulation of menaquinone (vitamin K2) biosynthesis in the human pathogenMycobacterium tuberculosis.
J.Biol.Chem., 295:3759-3770, 2020

PubMed Abstract: Menaquinone (vitamin K) plays a vital role in energy generation and environmental adaptation in many bacteria, including the human pathogen (). Although menaquinone levels are known to be tightly linked to the cellular redox/energy status of the cell, the regulatory mechanisms underpinning this phenomenon are unclear. The first committed step in menaquinone biosynthesis is catalyzed by MenD, a thiamine diphosphate-dependent enzyme comprising three domains. Domains I and III form the MenD active site, but no function has yet been ascribed to domain II. Here, we show that the last cytosolic metabolite in the menaquinone biosynthesis pathway, 1,4-dihydroxy-2-naphthoic acid (DHNA), binds to domain II of -MenD and inhibits its activity. Using X-ray crystallography of four apo- and cofactor-bound -MenD structures, along with several spectroscopy assays, we identified three arginine residues (Arg-97, Arg-277, and Arg-303) that are important for both enzyme activity and the feedback inhibition by DHNA. Among these residues, Arg-277 appeared to be particularly important for signal propagation from the allosteric site to the active site. This is the first evidence of feedback regulation of the menaquinone biosynthesis pathway in bacteria, identifying a protein-level regulatory mechanism that controls menaquinone levels within the cell and may therefore represent a good target for disrupting menaquinone biosynthesis in .

PubMed: 32029475
DOI: 10.1074/jbc.RA119.012158

実験手法

X-RAY DIFFRACTION (3.03 Å)