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9YHA

Cryo-EM structure of IDH1 R132H

9YHA の概要
エントリーDOI10.2210/pdb9yha/pdb
EMDBエントリー72964
分子名称Isocitrate dehydrogenase [NADP] cytoplasmic, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (2 entities in total)
機能のキーワードdehydrogenase, cellular metabolism, oxidative decarboxylation, cytosolic protein
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数2
化学式量合計97205.60
構造登録者
主引用文献Hu, L.,Lin, J.,Sun, L.,Berezuk, A.M.,Tuttle, K.S.,Zhu, X.,Seo, H.S.,Dhe-Paganon, S.,Li, P.,Sun, Y.,Ni, L.,Zhang, J.,Tan, D.,Wakimoto, H.,Cahill, D.P.,Bai, X.,Luo, X.,Asara, J.M.,Subramaniam, S.,Shan, Y.,Wu, X.
Autopalmitoylation of IDH1-R132H regulates its neomorphic activity in cancer cells.
Nat.Chem.Biol., 2026
Cited by
PubMed Abstract: Gain-of-function mutations of isocitrate dehydrogenase 1 (IDH1) lead to oncometabolite (R)-2-hydroxyglutarate production, contributing to the tumorigenesis of multiple human cancers. While fatty acid biosynthesis is critical for IDH1-mutant tumor growth, the underlying mechanisms remain unclear. Here, leveraging chemical probes and chemoproteomic profiling, we identified that oncogenic IDH1-R132H is uniquely autopalmitoylated at C269, which is not observed in wild-type IDH1. This modification responds to fatty acids and regulates R132H enzymatic activity by enhancing substrate and cofactor binding, as well as dimerization. Loss of C269 palmitoylation reverses IDH1-R132H-induced metabolic reprogramming and hypermethylation phenotypes and impairs cell transformation. Interestingly, C269 autopalmitoylation occurs within a hydrophobic pocket, targeted by a clinical IDH1-mutant inhibitor (LY3410738). Our study reveals that autopalmitoylation, conferred by the IDH1 mutation, links fatty acid metabolism to the regulation of IDH1 mutant activity and represents a druggable vulnerability in IDH1-mutant cancers.
PubMed: 41530531
DOI: 10.1038/s41589-025-02131-8
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.69 Å)
構造検証レポート
Validation report summary of 9yha
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2026-04-29に公開中

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