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- W4360778894 abstract "In this study, engineered imine reductases (IREDs) of IRED M5, originally from Actinoalloteichus hymeniacidonis, were obtained through structure-guided semi-rational design. By focusing on mutagenesis of the residues that directly interact with the ketone donor moiety, we identified two residues W234 and F260, playing essential roles in enhancing and reversing the stereoselectivity, respectively. Moreover, two completely enantio-complementary variants S241L/F260N (R-selectivity up to 99%) and I149D/W234I (S-selectivity up to 99%) were achieved. Both variants showed excellent stereoselectivity toward the tested substrates, offering valuable biocatalysts for synthesizing pyrrolidinamines. Its application was demonstrated in a short synthesis of the key intermediates of potential drug molecules leniolisib and JAK1 inhibitor 4, from cheap and commercially available pro-chiral N-Boc-piperidone 1 (2 and 3 steps, respectively)." @default.
- W4360778894 created "2023-03-25" @default.
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- W4360778894 date "2023-01-01" @default.
- W4360778894 modified "2023-10-09" @default.
- W4360778894 title "Structure-guided semi-rational design of an imine reductase for enantio-complementary synthesis of pyrrolidinamine" @default.
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- W4360778894 doi "https://doi.org/10.1039/d2sc07014f" @default.
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