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8E76

Cryo-EM structure of Apo form ME3

8E76 の概要
エントリーDOI10.2210/pdb8e76/pdb
EMDBエントリー27936
分子名称NADP-dependent malic enzyme, mitochondrial (1 entity in total)
機能のキーワードme1, me2, me3, nad(p)-dependent malic enzymes, integrated structural techniques, crystal structures, cryo-em structures, drug discovery, allosteric mechanism, hydrolase
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数4
化学式量合計268605.00
構造登録者
主引用文献Grell, T.A.J.,Mason, M.,Thompson, A.A.,Gomez-Tamayo, J.C.,Riley, D.,Wagner, M.V.,Steele, R.,Ortiz-Meoz, R.F.,Wadia, J.,Shaffer, P.L.,Tresadern, G.,Sharma, S.,Yu, X.
Integrative structural and functional analysis of human malic enzyme 3: A potential therapeutic target for pancreatic cancer.
Heliyon, 8:e12392-e12392, 2022
Cited by
PubMed Abstract: Malic enzymes (ME1, ME2, and ME3) are involved in cellular energy regulation, redox homeostasis, and biosynthetic processes, through the production of pyruvate and reducing agent NAD(P)H. Recent studies have implicated the third and least well-characterized isoform, mitochondrial NADP-dependent malic enzyme 3 (ME3), as a therapeutic target for pancreatic cancers. Here, we utilized an integrated structure approach to determine the structures of ME3 in various ligand-binding states at near-atomic resolutions. ME3 is captured in the open form existing as a stable tetramer and its dynamic Domain C is critical for activity. Catalytic assay results reveal that ME3 is a non-allosteric enzyme and does not require modulators for activity while structural analysis suggests that the inner stability of ME3 Domain A relative to ME2 disables allostery in ME3. With structural information available for all three malic enzymes, the foundation has been laid to understand the structural and biochemical differences of these enzymes and could aid in the development of specific malic enzyme small molecule drugs.
PubMed: 36590518
DOI: 10.1016/j.heliyon.2022.e12392
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.51 Å)
構造検証レポート
Validation report summary of 8e76
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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