9F08
Nucleoside-2'-deoxyribosyltransferase from Lactobacillus leichmannii. Covalent complex with 2-deoxyribose.
9F08 の概要
エントリーDOI | 10.2210/pdb9f08/pdb |
分子名称 | Nucleoside deoxyribosyltransferase, 2-deoxy-beta-D-erythro-pentofuranose (3 entities in total) |
機能のキーワード | nucleoside-2'-deoxyribosyltransferase, transferase |
由来する生物種 | Lactobacillus leichmannii |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 36464.97 |
構造登録者 | |
主引用文献 | Salihovic, A.,Ascham, A.,Taladriz-Sender, A.,Bryson, S.,Withers, J.M.,McKean, I.J.W.,Hoskisson, P.A.,Grogan, G.,Burley, G.A. Gram-scale enzymatic synthesis of 2'-deoxyribonucleoside analogues using nucleoside transglycosylase-2. Chem Sci, 15:15399-15407, 2024 Cited by PubMed Abstract: Nucleosides are pervasive building blocks that are found throughout nature and used extensively in medicinal chemistry and biotechnology. However, the preparation of base-modified analogues using conventional synthetic methodology poses challenges in scale-up and purification. In this work, an integrated approach involving structural analysis, screening and reaction optimization, is established to prepare 2'-deoxyribonucleoside analogues catalysed by the type II nucleoside 2'-deoxyribosyltransferase from (NDT-2). Structural analysis in combination with substrate profiling, identified the constraints on pyrimidine and purine acceptor bases by NDT2. A solvent screen identifies pure water as a suitable solvent for the preparation of high value purine and pyrimidine 2'-deoxyribonucleoside analogues on a gram scale under optimized reaction conditions. This approach provides the basis to establish a convergent, step-efficient chemoenzymatic platform for the preparation of high value 2'-deoxyribonucleosides. PubMed: 39234214DOI: 10.1039/d4sc04938a 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.371 Å) |
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