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7BSK

Crystal structure of human ME2 R67Q mutant

7BSK の概要
エントリーDOI10.2210/pdb7bsk/pdb
分子名称NAD-dependent malic enzyme, mitochondrial, NICOTINAMIDE-ADENINE-DINUCLEOTIDE (3 entities in total)
機能のキーワードmalate dehydrogenase, nad-dependent malic enzyme, hydrolase
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129607.54
構造登録者
Chen, W.L.,Tai, S.C.,Hung, H.C.,Ho, M.C. (登録日: 2020-03-30, 公開日: 2021-02-10, 最終更新日: 2023-11-29)
主引用文献Hsieh, J.Y.,Yang, H.P.,Tewary, S.K.,Cheng, H.C.,Liu, Y.L.,Tai, S.C.,Chen, W.L.,Hsu, C.H.,Huang, T.J.,Chou, C.J.,Huang, Y.N.,Peng, C.T.,Ho, M.C.,Liu, G.Y.,Hung, H.C.
Single nucleotide variants lead to dysregulation of the human mitochondrial NAD(P) + -dependent malic enzyme.
Iscience, 24:102034-102034, 2021
Cited by
PubMed Abstract: Human mitochondrial NAD(P)-dependent malic enzyme (ME2) is well recognized to associate with cancer cell metabolism, and the single nucleotide variants (SNVs) of ME2 may play a role in enzyme regulation. Here we reported that the SNVs of ME2 occurring in the allosteric sites lead to inactivation or overactivation of ME2. Two ME2-SNVs, ME2_R67Q and ME2-R484W, that demonstrated inactivating or overactivating enzyme activities of ME2, respectively, have different impact toward the cells. The cells with overactivating SNV enzyme, ME2_R484W, grow more rapidly and are more resistant to cellular senescence than the cells with wild-type or inactivating SNV enzyme, ME2_R67Q. Crystal structures of these two ME2-SNVs reveal that ME2_R67Q was an inactivating "dead form," and ME2_R484W was an overactivating "closed form" of the enzyme. The resolved ME2-SNV structures provide a molecular basis to explain the abnormal kinetic properties of these SNV enzymes.
PubMed: 33554057
DOI: 10.1016/j.isci.2021.102034
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.55 Å)
構造検証レポート
Validation report summary of 7bsk
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2026-04-15に公開中

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