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结核分枝杆菌细胞色素 P450 体系中的潜在药物靶点。

Potential drug targets in the Mycobacterium tuberculosis cytochrome P450 system.

机构信息

Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94143, United States.

出版信息

J Inorg Biochem. 2018 Mar;180:235-245. doi: 10.1016/j.jinorgbio.2018.01.010. Epub 2018 Jan 12.

Abstract

The Mycobacterium tuberculosis genome encodes twenty cytochrome P450 enzymes, most or all of which appear to have specific physiological functions rather than being devoted to the removal of xenobiotics. However, in many cases their specific functions remain obscure. Considerable spectroscopic, biophysical, crystallographic, and catalytic information is available on nine of these cytochrome P450 enzymes, although gaps exist in our knowledge of even these enzymes. The available evidence indicates that at least three of the better-characterized enzymes are promising targets for antituberculosis drug discovery. This review summarizes the information on the nine relatively well-characterized cytochrome P450 enzymes, with a particular emphasis on CYP121, CYP125, and CYP142 from Mycobacterium tuberculosis and Mycobacterium smegmatis.

摘要

结核分枝杆菌基因组编码二十种细胞色素 P450 酶,其中大多数或全部似乎都具有特定的生理功能,而不是专门用于去除外来物质。然而,在许多情况下,它们的具体功能仍然不清楚。尽管我们对这些酶的了解仍存在空白,但已经有相当数量的光谱学、生物物理学、晶体学和催化信息可用于其中的九种细胞色素 P450 酶。现有证据表明,至少有三种研究更为透彻的酶是有希望的抗结核药物发现靶点。这篇综述总结了关于这九种相对研究透彻的细胞色素 P450 酶的信息,特别强调结核分枝杆菌和耻垢分枝杆菌中的 CYP121、CYP125 和 CYP142。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/257f/5801126/e7e14fa45d83/nihms935064f1.jpg

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