2YPQ

3-deoxy-D-arabino-heptulosonate 7-phosphate synthase with tryptophan and tyrosine bound

2YPQ の概要

• エントリーDOI: 10.2210/pdb2ypq/pdb
• 関連するPDBエントリー: 2YPO 2YPP
• 分子名称: PHOSPHO-2-DEHYDRO-3-DEOXYHEPTONATE ALDOLASE AROG, TYROSINE, MANGANESE (II) ION, ... (9 entities in total)
• 機能のキーワード: shikimate pathway, transferase, aromatic amino acid biosynthesis, allostery
• 由来する生物種: MYCOBACTERIUM TUBERCULOSIS
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 103283.78

構造登録者

Blackmore, N.J.,Reichau, S.,Jiao, W.,Hutton, R.D.,Baker, E.N.,Jameson, G.B.,Parker, E.J. (登録日: 2012-10-31, 公開日: 2013-01-09, 最終更新日: 2023-12-20)

主引用文献

Blackmore, N.J.,Reichau, S.,Jiao, W.,Hutton, R.D.,Baker, E.N.,Jameson, G.B.,Parker, E.J.
Three Sites and You are Out: Ternary Synergistic Allostery Controls Aromatic Aminoacid Biosynthesis in Mycobacterium Tuberculosis.
J.Mol.Biol., 425:1582-, 2013

PubMed Abstract: 3-Deoxy-d-arabino-heptulosonate 7-phosphate synthase (DAH7PS) catalyzes the first step in the shikimate pathway, the pathway responsible for the biosynthesis of the aromatic amino acids Trp, Phe, and Tyr. Unlike many other organisms that produce up to three isozymes, each feedback-regulated by one of the aromatic amino acid pathway end products, Mycobacterium tuberculosis expresses a single DAH7PS enzyme that can be controlled by combinations of aromatic amino acids. This study shows that the synergistic inhibition of this enzyme by a combination of Trp and Phe can be significantly augmented by the addition of Tyr. We used X-ray crystallography, mutagenesis, and isothermal titration calorimetry studies to show that DAH7PS from M. tuberculosis possesses a Tyr-selective site in addition to the Trp and Phe sites, revealing an unusual and highly sophisticated network of three synergistic allosteric sites on one enzyme. This ternary inhibitory response, by a combination of all three aromatic amino acids, allows a tunable response of the protein to changing metabolic demands.

PubMed: 23274137
DOI: 10.1016/J.JMB.2012.12.019

実験手法

X-RAY DIFFRACTION (2.76 Å)