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核碱基脱氨酶:一种用于新疗法的潜在酶系统。

Nucleobase deaminases: a potential enzyme system for new therapies.

作者信息

Gaded Vandana, Anand Ruchi

机构信息

Department of Chemistry, Indian Institute of Technology Bombay Mumbai Maharashtra 400076 India

出版信息

RSC Adv. 2018 Jun 28;8(42):23567-23577. doi: 10.1039/c8ra04112a. eCollection 2018 Jun 27.

Abstract

Nucleobase deaminases are essential enzymes that are involved in the catabolic pathway and stringently regulate the concentration of the nucleobase derivative pool, which is paramount for nucleotide recycling. This review presents an overview of the structure, function and mechanism of CDA deaminases and their potential as enzyme systems for the development of new antimicrobial therapies. The evolutionary divergence of human nucleobase deaminases with respect to bacterial enzymes has been used as a central theme towards the development of strategies for potential drug targets. Especially, differences in their tertiary fold, active site architectures and mechanisms of regulation have been highlighted in this study. Overall, deaminases present a unique opportunity as drug targets because of their functional plasticity and fidelity.

摘要

核碱基脱氨酶是参与分解代谢途径的关键酶,严格调控核碱基衍生物池的浓度,这对于核苷酸循环至关重要。本综述概述了胞嘧啶脱氨酶的结构、功能和作用机制,以及它们作为新型抗菌疗法开发酶系统的潜力。人类核碱基脱氨酶与细菌酶在进化上的差异已被用作开发潜在药物靶点策略的核心主题。特别是,本研究突出了它们三级结构、活性位点结构和调控机制的差异。总体而言,脱氨酶因其功能可塑性和专一性而成为独特的药物靶点。

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