College of Pharmacy, Chung-Ang University, Dongjak-gu, Seoul 06974, Republic of Korea.
Unit of Research for Practical Application, Korea Polar Research Institute, Incheon 21990, Republic of Korea.
Acta Crystallogr F Struct Biol Commun. 2020 Aug 1;76(Pt 8):364-371. doi: 10.1107/S2053230X20009735. Epub 2020 Jul 28.
Aminoglycoside acetyltransferases (AACs) catalyze the transfer of an acetyl group between acetyl-CoA and an aminoglycoside, producing CoA and an acetylated aminoglycoside. AAC(6')-Ii enzymes target the amino group linked to the 6' C atom in an aminoglycoside. Several structures of the AAC(6')-Ii from Enterococcus faecium [Ef-AAC(6')-Ii] have been reported to date. However, the detailed mechanism of its enzymatic function remains elusive. In this study, the crystal structure of Ef-AAC(6')-Ii was determined in a novel substrate-free form. Based on structural analysis, it is proposed that Ef-AAC(6')-Ii sequentially undergoes conformational selection and induced fit for substrate binding. These results therefore provide a novel viewpoint on the mechanism of action of Ef-AAC(6')-Ii.
氨基糖苷乙酰转移酶(AACs)催化乙酰辅酶 A 和氨基糖苷之间的乙酰基转移,生成辅酶 A 和乙酰化的氨基糖苷。AAC(6')-Ii 酶靶向氨基糖苷中与 6' C 原子相连的氨基。迄今为止,已经报道了几种屎肠球菌 AAC(6')-Ii(Ef-AAC(6')-Ii)的结构。然而,其酶促功能的详细机制仍不清楚。在这项研究中,确定了新型无底物形式的 Ef-AAC(6')-Ii 的晶体结构。基于结构分析,提出 Ef-AAC(6')-Ii 依次经历构象选择和诱导契合以结合底物。因此,这些结果为 Ef-AAC(6')-Ii 的作用机制提供了新的视角。