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非核糖体肽合成酶腺苷化结构域的结构、生化及生物信息学分析

Structural, biochemical and bioinformatic analyses of nonribosomal peptide synthetase adenylation domains.

作者信息

Heard Stephanie C, Winter Jaclyn M

机构信息

Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT 84112, USA.

出版信息

Nat Prod Rep. 2024 Jul 17;41(7):1180-1205. doi: 10.1039/d3np00064h.

Abstract

Covering: 1997 to July 2023The adenylation reaction has been a subject of scientific intrigue since it was first recognized as essential to many biological processes, including the homeostasis and pathogenicity of some bacteria and the activation of amino acids for protein synthesis in mammals. Several foundational studies on adenylation (A) domains have facilitated an improved understanding of their molecular structures and biochemical properties, in particular work on nonribosomal peptide synthetases (NRPSs). In NRPS pathways, A domains activate their respective acyl substrates for incorporation into a growing peptidyl chain, and many nonribosomal peptides are bioactive. From a natural product drug discovery perspective, improving existing bioinformatics platforms to predict unique NRPS products more accurately from genomic data is desirable. Here, we summarize characterization efforts of A domains primarily from NRPS pathways from July 1997 up to July 2023, covering protein structure elucidation, assay development, and tools for improved predictions.

摘要

涵盖时间

1997年至2023年7月

自腺苷化反应首次被认为对许多生物过程至关重要以来,它一直是科学研究的热点,这些生物过程包括某些细菌的体内平衡和致病性,以及哺乳动物蛋白质合成中氨基酸的活化。关于腺苷化(A)结构域的几项基础研究有助于更好地理解其分子结构和生化特性,特别是关于非核糖体肽合成酶(NRPS)的研究。在NRPS途径中,A结构域激活各自的酰基底物以掺入不断增长的肽基链中,许多非核糖体肽具有生物活性。从天然产物药物发现的角度来看,改进现有的生物信息学平台以从基因组数据中更准确地预测独特的NRPS产物是很有必要的。在这里,我们总结了1997年7月至2023年7月主要来自NRPS途径的A结构域的表征工作,包括蛋白质结构解析、检测方法开发以及用于改进预测的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fa9/11253843/81c18db2d85d/d3np00064h-f1.jpg

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