Carreras C W, Santi D V
Department of Pharmaceutical Chemistry, University of California San Francisco 94143-0448, USA.
Annu Rev Biochem. 1995;64:721-62. doi: 10.1146/annurev.bi.64.070195.003445.
Thymidylate synthase (TS, EC 2.1.1.45) catalyzes the reductive methylation of dUMP by CH2H4folate to produce dTMP and H2folate. Knowledge of the catalytic mechanism and structure of TS has increased substantially over recent years. Major advances were derived from crystal structures of TS bound to various ligands, the ability to overexpress TS in heterologous hosts, and the numerous mutants that have been prepared and analyzed. These advances, coupled with previous knowledge, have culminated in an in-depth understanding of many important molecular details of the reaction. We review aspects of TS catalysis that are most pertinent to understanding the current status of the structure and catalytic mechanism of the enzyme. Included is a discussion of available sources and assays for TS, a description of the enzyme's chemical mechanism and crystal structure, and a summary of data obtained from mutagenesis experiments.
胸苷酸合成酶(TS,EC 2.1.1.45)催化二氢叶酸(CH2H4folate)将脱氧尿苷一磷酸(dUMP)还原甲基化,生成脱氧胸苷一磷酸(dTMP)和二氢叶酸(H2folate)。近年来,人们对胸苷酸合成酶的催化机制和结构的了解有了大幅增加。主要进展来自与各种配体结合的胸苷酸合成酶的晶体结构、在异源宿主中过表达胸苷酸合成酶的能力,以及制备和分析的众多突变体。这些进展与先前的知识相结合,最终使人们对该反应的许多重要分子细节有了深入的了解。我们回顾了与理解该酶的结构和催化机制的当前状况最相关的胸苷酸合成酶催化的各个方面。内容包括对胸苷酸合成酶的可用来源和检测方法的讨论、对该酶化学机制和晶体结构的描述,以及从诱变实验获得的数据的总结。