5YVT

Crystal structure of the alpha gamma heterodimer of human IDH3 in complex with Mg(2+) and NADH

5YVT の概要

• エントリーDOI: 10.2210/pdb5yvt/pdb
• 分子名称: Isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial, Isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial, MAGNESIUM ION, ... (5 entities in total)
• 機能のキーワード: nadh, inhibition, oxidoreductase
• 由来する生物種: Homo sapiens (Human); 詳細
• 細胞内の位置: Mitochondrion: P50213 P51553
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 76904.89

構造登録者

Ma, T.,Ding, J. (登録日: 2017-11-27, 公開日: 2018-03-14, 最終更新日: 2023-11-22)

主引用文献

Liu, Y.,Hu, L.,Ma, T.,Yang, J.,Ding, J.
Insights into the inhibitory mechanisms of NADH on the alpha gamma heterodimer of human NAD-dependent isocitrate dehydrogenase.
Sci Rep, 8:3146-3146, 2018

PubMed Abstract: Human NAD-dependent isocitrate dehydrogenase (NAD-IDH) catalyzes the oxidative decarboxylation of isocitrate in the citric acid cycle. In the αβγ heterotetramer of NAD-IDH, the γ subunit plays the regulatory role and the β subunit the structural role. Previous biochemical data have shown that mammalian NAD-IDHs can be inhibited by NADH; however, the molecular mechanism is unclear. In this work, we show that the αβ, αγ and αβγ enzymes of human NAD-IDH can be inhibited by NADH, and further determine the crystal structure of the αγ heterodimer bound with an Mg and an NADH at the active site and an NADH at the allosteric site, which resembles that of the inactive αγ heterodimer. The NADH at the active site occupies the binding site for NAD and prevents the binding of the cofactor. The NADH at the allosteric site occupies the binding sites for ADP and citrate and blocks the binding of the activators. The biochemical data confirm that the NADH binding competes with the binding of NAD and the binding of citrate and ADP, and the two effects together contribute to the NADH inhibition on the activity. These findings provide insights into the inhibitory mechanisms of the αγ heterodimer by NADH.

PubMed: 29453450
DOI: 10.1038/s41598-018-21584-7

実験手法

X-RAY DIFFRACTION (2.4 Å)