7XR5
Crystal structure of imine reductase with NAPDH from Streptomyces albidoflavus
7XR5 の概要
エントリーDOI | 10.2210/pdb7xr5/pdb |
分子名称 | 6-phosphogluconate dehydrogenase NAD-binding, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, 3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51,54,57-nonadecaoxanonapentacontane-1,59-diol, ... (4 entities in total) |
機能のキーワード | streptomyces albidoflavus, nadp, r-imine reductase, oxidoreductase |
由来する生物種 | Streptomyces albidoflavus |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 134485.92 |
構造登録者 | |
主引用文献 | Zhang, J.,Li, X.,Chen, R.,Tan, X.,Liu, X.,Ma, Y.,Zhu, F.,An, C.,Wei, G.,Yao, Y.,Yang, L.,Zhang, P.,Wu, Q.,Sun, Z.,Wang, B.G.,Gao, S.S.,Cui, C. Actinomycetes-derived imine reductases with a preference towards bulky amine substrates. Commun Chem, 5:123-123, 2022 Cited by PubMed Abstract: Since imine reductases (IREDs) were reported to catalyze the reductive amination reactions, they became particularly attractive for producing chiral amines. Though diverse ketones and aldehydes have been proved to be excellent substrates of IREDs, bulky amines have been rarely transformed. Here we report the usage of an Increasing-Molecule-Volume-Screening to identify a group of IREDs (IR-G02, 21, and 35) competent for accepting bulky amine substrates. IR-G02 shows an excellent substrate scope, which is applied to synthesize over 135 amine molecules as well as a range of APIs' substructures. The crystal structure of IR-G02 reveals the determinants for altering the substrate preference. Finally, we demonstrate a gram-scale synthesis of an analogue of the API sensipar via a kinetic resolution approach, which displays ee >99%, total turnover numbers of up to 2087, and space time yield up to 18.10 g L d. PubMed: 36697820DOI: 10.1038/s42004-022-00743-y 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.58 Å) |
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