6FPS
Crystal structure of 4-oxalocrotonate tautomerase triple mutant L8Y/M45Y/F50A
6FPS の概要
| エントリーDOI | 10.2210/pdb6fps/pdb |
| 分子名称 | 2-hydroxymuconate tautomerase, PHOSPHATE ION, GLYCEROL, ... (4 entities in total) |
| 機能のキーワード | 2-hydroxymuconate tautomerase, isomerase |
| 由来する生物種 | Pseudomonas putida (Arthrobacter siderocapsulatus) |
| タンパク質・核酸の鎖数 | 18 |
| 化学式量合計 | 123086.31 |
| 構造登録者 | |
| 主引用文献 | Biewenga, L.,Saravanan, T.,Kunzendorf, A.,van der Meer, J.Y.,Pijning, T.,Tepper, P.G.,van Merkerk, R.,Charnock, S.J.,Thunnissen, A.W.H.,Poelarends, G.J. Enantioselective Synthesis of Pharmaceutically Active gamma-Aminobutyric Acids Using a Tailor-Made Artificial Michaelase in One-Pot Cascade Reactions. ACS Catal, 9:1503-1513, 2019 Cited by PubMed Abstract: Chiral γ-aminobutyric acid (GABA) analogues represent abundantly prescribed drugs, which are broadly applied as anticonvulsants, as antidepressants, and for the treatment of neuropathic pain. Here we report a one-pot two-step biocatalytic cascade route for synthesis of the pharmaceutically relevant enantiomers of γ-nitrobutyric acids, starting from simple precursors (acetaldehyde and nitroalkenes), using a tailor-made highly enantioselective artificial "Michaelase" (4-oxalocrotonate tautomerase mutant L8Y/M45Y/F50A), an aldehyde dehydrogenase with a broad non-natural substrate scope, and a cofactor recycling system. We also report a three-step chemoenzymatic cascade route for the efficient chemical reduction of enzymatically prepared γ-nitrobutyric acids into GABA analogues in one pot, achieving high enantiopurity (e.r. up to 99:1) and high overall yields (up to 70%). This chemoenzymatic methodology offers a step-economic alternative route to important pharmaceutically active GABA analogues, and highlights the exciting opportunities available for combining chemocatalysts, natural enzymes, and designed artificial biocatalysts in multistep syntheses. PubMed: 30740262DOI: 10.1021/acscatal.8b04299 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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