Neisseria gonorrhoeae carbonic anhydrase inhibition.

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2024-01-01 Epub Date: 2024-06-06 DOI:10.1016/bs.enz.2024.05.008
Molly S Youse, Katrina J Holly, Daniel P Flaherty
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引用次数: 0

Abstract

Carbonic anhydrases (CAs) are ubiquitous enzymes that are found in all kingdoms of life. Though different classes of CAs vary in their roles and structures, their primary function is to catalyze the reaction between carbon dioxide and water to produce bicarbonate and a proton. Neisseria gonorrhoeae encodes for three distinct CAs (NgCAs) from three different families: an α-, a β-, and a γ-isoform. This chapter details the differences between the three NgCAs, summarizing their subcellular locations, roles, essentiality, structures, and enzyme kinetics. These bacterial enzymes have the potential to be drug targets; thus, previous studies have investigated the inhibition of NgCAs-primarily the α-isoform. Therefore, the classes of inhibitors that have been shown to bind to the NgCAs will be discussed as well. These classes include traditional CA inhibitors, such as sulfonamides, phenols, and coumarins, as well as non-traditional inhibitors including anions and thiocarbamates.

淋病奈瑟菌碳酸酐酶抑制剂。
碳酸酐酶(CA)是一种无处不在的酶,存在于所有生物界中。尽管不同种类的 CAs 在作用和结构上各不相同,但它们的主要功能是催化二氧化碳和水之间的反应,生成碳酸氢盐和质子。淋病奈瑟菌编码来自三个不同家族的三种不同的 CA(NgCAs):α-、β- 和 γ-异构体。本章将详细介绍这三种 NgCA 的区别,总结它们的亚细胞位置、作用、本质、结构和酶动力学。这些细菌酶有可能成为药物靶标;因此,以前的研究已对 NgCA(主要是 α-异构体)的抑制作用进行了调查。因此,我们也将讨论已证明能与 NgCAs 结合的抑制剂类别。这些抑制剂包括磺胺类、酚类和香豆素类等传统 CA 抑制剂,以及阴离子和硫代氨基甲酸酯类等非传统抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
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