3B6Z
Lovastatin polyketide enoyl reductase (LovC) complexed with 2'-phosphoadenosyl isomer of crotonoyl-CoA
3B6Z の概要
| エントリーDOI | 10.2210/pdb3b6z/pdb |
| 関連するPDBエントリー | 3B70 |
| 分子名称 | Enoyl reductase, S-{(9R,13R,15S)-17-[(2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-hydroxy-4-(phosphonooxy)tetrahydrofuran-2-yl]-9,13,15-trihydroxy-10,10-dimethyl-13,15-dioxido-4,8-dioxo-12,14,16-trioxa-3,7-diaza-13,15-diphosphaheptadec-1-yl}(2E)-but-2-enethioate, GLYCEROL, ... (4 entities in total) |
| 機能のキーワード | medium-chain reductase, rossmann fold, nadp-binding, oxidoreductase |
| 由来する生物種 | Aspergillus terreus |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 41550.59 |
| 構造登録者 | Ames, B.D.,Smith, P.T.,Ma, S.M.,Wong, E.W.,Xie, X.,Vederas, J.C.,Tang, Y.,Tsai, S.-C. (登録日: 2007-10-29, 公開日: 2008-09-16, 最終更新日: 2024-02-21) |
| 主引用文献 | Ames, B.D.,Nguyen, C.,Bruegger, J.,Smith, P.,Xu, W.,Ma, S.,Wong, E.,Wong, S.,Xie, X.,Li, J.W.,Vederas, J.C.,Tang, Y.,Tsai, S.C. Crystal structure and biochemical studies of the trans-acting polyketide enoyl reductase LovC from lovastatin biosynthesis. Proc.Natl.Acad.Sci.USA, 109:11144-11149, 2012 Cited by PubMed Abstract: Lovastatin is an important statin prescribed for the treatment and prevention of cardiovascular diseases. Biosynthesis of lovastatin uses an iterative type I polyketide synthase (PKS). LovC is a trans-acting enoyl reductase (ER) that specifically reduces three out of eight possible polyketide intermediates during lovastatin biosynthesis. Such trans-acting ERs have been reported across a variety of other fungal PKS enzymes as a strategy in nature to diversify polyketides. How LovC achieves such specificity is unknown. The 1.9-Å structure of LovC reveals that LovC possesses a medium-chain dehydrogenase/reductase (MDR) fold with a unique monomeric assembly. Two LovC cocrystal structures and enzymological studies help elucidate the molecular basis of LovC specificity, define stereochemistry, and identify active-site residues. Sequence alignment indicates a general applicability to trans-acting ERs of fungal PKSs, as well as their potential application to directing biosynthesis. PubMed: 22733743DOI: 10.1073/pnas.1113029109 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.88 Å) |
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