8AEP
Reductase domain of the carboxylate reductase of Neurospora crassa
8AEP の概要
| エントリーDOI | 10.2210/pdb8aep/pdb |
| 分子名称 | Acetyl-CoA synthetase-like protein, CHLORIDE ION, SULFATE ION, ... (4 entities in total) |
| 機能のキーワード | oxidereductase, carboxylate reductase, oxidoreductase |
| 由来する生物種 | Neurospora crassa |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 90068.03 |
| 構造登録者 | Daniel, B.,Schrufer, A.,Marlene, L.,Sagmeister, T.,Pavkov-Keller, T. (登録日: 2022-07-13, 公開日: 2023-03-08, 最終更新日: 2024-02-07) |
| 主引用文献 | Daniel, B.,Hashem, C.,Leithold, M.,Sagmeister, T.,Tripp, A.,Stolterfoht-Stock, H.,Messenlehner, J.,Keegan, R.,Winkler, C.K.,Ling, J.G.,Younes, S.H.H.,Oberdorfer, G.,Abu Bakar, F.D.,Gruber, K.,Pavkov-Keller, T.,Winkler, M. Structure of the Reductase Domain of a Fungal Carboxylic Acid Reductase and Its Substrate Scope in Thioester and Aldehyde Reduction. Acs Catalysis, 12:15668-15674, 2022 Cited by PubMed Abstract: The synthesis of aldehydes from carboxylic acids has long been a challenge in chemistry. In contrast to the harsh chemically driven reduction, enzymes such as carboxylic acid reductases (CARs) are considered appealing biocatalysts for aldehyde production. Although structures of single- and didomains of microbial CARs have been reported, to date no full-length protein structure has been elucidated. In this study, we aimed to obtain structural and functional information regarding the reductase (R) domain of a CAR from the fungus (). The CAR R-domain revealed activity for -acetylcysteamine thioester (S-(2-acetamidoethyl) benzothioate), which mimics the phosphopantetheinylacyl-intermediate and can be anticipated as the minimal substrate for thioester reduction by CARs. The determined crystal structure of the CAR R-domain reveals a tunnel that putatively harbors the phosphopantetheinylacyl-intermediate, which is in good agreement with docking experiments performed with the minimal substrate. studies were performed with this highly purified R-domain and NADPH, demonstrating carbonyl reduction activity. The R-domain was able to accept not only a simple aromatic ketone but also benzaldehyde and octanal, which are typically considered to be the final product of carboxylic acid reduction by CAR. Also, the full-length CAR reduced aldehydes to primary alcohols. In conclusion, aldehyde overreduction can no longer be attributed exclusively to the host background. PubMed: 37180375DOI: 10.1021/acscatal.2c04426 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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