Shenoy Avinash R, Visweswariah Sandhya S
Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore.
FEBS Lett. 2006 Jun 12;580(14):3344-52. doi: 10.1016/j.febslet.2006.05.034. Epub 2006 May 22.
The conversion of adenine and guanine nucleoside triphosphates to cAMP and cGMP is carried out by nucleotide cyclases, which vary in their primary sequence and are therefore grouped into six classes. The class III enzymes encompass all eukaryotic adenylyl and guanylyl cyclase, and several bacterial and archaebacterial cyclases. Mycobacterial nucleotide cyclases show distinct biochemical properties and domain fusions, and we review here biochemical and structural studies on these enzymes from Mycobacterium tuberculosis and related bacteria. We also present an in silico analysis of nucleotide cyclases found in completely sequenced mycobacterial genomes. It is clear that this group of enzymes demonstrates the tinkering in the class III cyclase domain during evolution, involving subtle structural changes that retain the overall catalytic function and fine tune their activities.
腺嘌呤和鸟嘌呤核苷三磷酸转化为环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)是由核苷酸环化酶完成的,这些酶的一级序列各不相同,因此被分为六类。III类酶包括所有真核腺苷酸环化酶和鸟苷酸环化酶,以及几种细菌和古细菌环化酶。分枝杆菌核苷酸环化酶具有独特的生化特性和结构域融合,我们在此综述来自结核分枝杆菌及相关细菌的这些酶的生化和结构研究。我们还对完全测序的分枝杆菌基因组中发现的核苷酸环化酶进行了计算机分析。很明显,这组酶在进化过程中展示了III类环化酶结构域的修补,涉及细微的结构变化,这些变化保留了整体催化功能并微调了它们的活性。