5Z8K
Crystal structure of an aminotransferase in complex with product-1
5Z8K の概要
エントリーDOI | 10.2210/pdb5z8k/pdb |
分子名称 | C-6' aminotransferase, PYRIDOXAL-5'-PHOSPHATE, (1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl 2,6-diamino-2,6-dideoxy-alpha-D-glucopyranoside, ... (4 entities in total) |
機能のキーワード | aminotransferase, transferase |
由来する生物種 | Micromonospora echinospora (Micromonospora purpurea) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 95487.81 |
構造登録者 | |
主引用文献 | Ban, Y.H.,Song, M.C.,Hwang, J.Y.,Shin, H.L.,Kim, H.J.,Hong, S.K.,Lee, N.J.,Park, J.W.,Cha, S.S.,Liu, H.W.,Yoon, Y.J. Complete reconstitution of the diverse pathways of gentamicin B biosynthesis. Nat. Chem. Biol., 15:295-303, 2019 Cited by PubMed Abstract: Gentamicin B (GB), a valuable starting material for the preparation of the semisynthetic aminoglycoside antibiotic isepamicin, is produced in trace amounts by the wild-type Micromonospora echinospora. Though the biosynthetic pathway to GB has remained obscure for decades, we have now identified three hidden pathways to GB production via seven hitherto unknown intermediates in M. echinospora. The narrow substrate specificity of a key glycosyltransferase and the C6'-amination enzymes, in combination with the weak and unsynchronized gene expression of the 2'-deamination enzymes, limits GB production in M. echinospora. The crystal structure of the aminotransferase involved in C6'-amination explains its substrate specificity. Some of the new intermediates displayed similar premature termination codon readthrough activity but with reduced toxicity compared to the natural aminoglycoside G418. This work not only led to the discovery of unknown biosynthetic routes to GB, but also demonstrated the potential to mine new aminoglycosides from nature for drug discovery. PubMed: 30643280DOI: 10.1038/s41589-018-0203-4 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.759 Å) |
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