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6ORA

An Unexpected Intermediate in the Reaction Catalyzed by Quinolinate Synthase

6ORA の概要
エントリーDOI10.2210/pdb6ora/pdb
関連するPDBエントリー4ZK6 4ZKZ 5FEV 5FFK 6NSO 6NSU
分子名称Quinolinate synthase A, IRON/SULFUR CLUSTER, ACETATE ION, ... (7 entities in total)
機能のキーワードbiosynthesis, transferase
由来する生物種Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3)
タンパク質・核酸の鎖数2
化学式量合計69694.67
構造登録者
Esakova, O.A.,Grove, T.L.,Silakov, A.,Yennawar, N.H.,Booker, S.J. (登録日: 2019-04-29, 公開日: 2019-08-21, 最終更新日: 2023-10-11)
主引用文献Esakova, O.A.,Silakov, A.,Grove, T.L.,Warui, D.M.,Yennawar, N.H.,Booker, S.J.
An Unexpected Species Determined by X-ray Crystallography that May Represent an Intermediate in the Reaction Catalyzed by Quinolinate Synthase.
J.Am.Chem.Soc., 141:14142-14151, 2019
Cited by
PubMed Abstract: Quinolinic acid is a common intermediate in the biosynthesis of nicotinamide adenine dinucleotide and its derivatives in all organisms that synthesize the molecule de novo. In most prokaryotes, it is formed from the condensation of dihydroxyacetone phosphate (DHAP) and iminoaspartate (IA) by the action of quinolinate synthase (NadA). NadA contains a [4Fe-4S] cluster cofactor with a unique noncysteinyl-ligated iron ion (Fe), which is proposed to bind the hydroxyl group of an intermediate in its reaction to facilitate a dehydration step. However, direct evidence for this role in catalysis has yet to be provided, and the exact chemical mechanism that underlies this transformation remains elusive. Herein, we present a structure of NadA from (PhNadA) in complex with IA and show that a carboxylate group of the molecule is ligated to Fe of the iron-sulfur cluster, occupying the site to which DHAP has been proposed to bind during catalysis. When crystals of PhNadA in complex with IA are soaked briefly in DHAP before freezing, electron density for a new molecule is observed, which we suggest is related to an intermediate in the reaction. Similar, but slightly different, "intermediates" are observed when crystals of a PhNadA Glu198Gln variant are incubated with DHAP, oxaloacetate, and ammonium chloride, conditions under which IA is formed chemically. Continuous-wave and pulse electron paramagnetic resonance techniques are used to verify the binding mode of substrates and proposed intermediates in frozen solution.
PubMed: 31390192
DOI: 10.1021/jacs.9b02513
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 6ora
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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