1F12
L-3-HYDROXYACYL-COA DEHYDROGENASE COMPLEXED WITH 3-HYDROXYBUTYRYL-COA
1F12 の概要
| エントリーDOI | 10.2210/pdb1f12/pdb |
| 関連するPDBエントリー | 1F0Y 1F14 1F17 3HAD |
| 分子名称 | L-3-HYDROXYACYL-COA DEHYDROGENASE, 3-HYDROXYBUTANOYL-COENZYME A (3 entities in total) |
| 機能のキーワード | l-3-hydroxyacyl-coa complexed with 3-hydroxybutyryl-coa, oxidoreductase |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Mitochondrion matrix: Q16836 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 68645.27 |
| 構造登録者 | Barycki, J.J.,O'Brien, L.K.,Strauss, A.W.,Banaszak, L.J. (登録日: 2000-05-18, 公開日: 2000-09-27, 最終更新日: 2024-02-07) |
| 主引用文献 | Barycki, J.J.,O'Brien, L.K.,Strauss, A.W.,Banaszak, L.J. Sequestration of the active site by interdomain shifting. Crystallographic and spectroscopic evidence for distinct conformations of L-3-hydroxyacyl-CoA dehydrogenase. J.Biol.Chem., 275:27186-27196, 2000 Cited by PubMed Abstract: l-3-Hydroxyacyl-CoA dehydrogenase reversibly catalyzes the conversion of l-3-hydroxyacyl-CoA to 3-ketoacyl-CoA concomitant with the reduction of NAD(+) to NADH as part of the beta-oxidation spiral. In this report, crystal structures have been solved for the apoenzyme, binary complexes of the enzyme with reduced cofactor or 3-hydroxybutyryl-CoA substrate, and an abortive ternary complex of the enzyme with NAD(+) and acetoacetyl-CoA. The models illustrate positioning of cofactor and substrate within the active site of the enzyme. Comparison of these structures with the previous model of the enzyme-NAD(+) complex reveals that although significant shifting of the NAD(+)-binding domain relative to the C-terminal domain occurs in the ternary and substrate-bound complexes, there are few differences between the apoenzyme and cofactor-bound complexes. Analysis of these models clarifies the role of key amino acids implicated in catalysis and highlights additional critical residues. Furthermore, a novel charge transfer complex has been identified in the course of abortive ternary complex formation, and its characterization provides additional insight into aspects of the catalytic mechanism of l-3-hydroxyacyl-CoA dehydrogenase. PubMed: 10840044主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.4 Å) |
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