8EYN
Crystal Structure of Human Mitochondrial NADP+ Malic Enzyme 3 in Apo Form
8EYN の概要
エントリーDOI | 10.2210/pdb8eyn/pdb |
分子名称 | NADP-dependent malic enzyme, mitochondrial, CITRIC ACID (3 entities in total) |
機能のキーワード | oxidoreductase, malic enzyme, rossmann fold, me3, nadp(+)-binding |
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 | 128042.95 |
構造登録者 | Shaffer, P.L.,Grell, T.A.J.,Mason, M.,Thompson, A.A.,Riley, D.,Wagner, M.V.,Steele, R.,Ortiz-Meoz, R.,Wadia, J.,Sharma, S.,Yu, X. (登録日: 2022-10-28, 公開日: 2023-02-08, 最終更新日: 2023-10-25) |
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: 36590518DOI: 10.1016/j.heliyon.2022.e12392 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.94 Å) |
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