把氨基酸放到trna上:氨酰基- trna合成酶作为催化剂。

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2020-01-01 Epub Date: 2020-09-08 DOI:10.1016/bs.enz.2020.06.003
Rebecca W Alexander, Tamara L Hendrickson
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引用次数: 0

摘要

在本章中,我们考虑了氨基酰基tRNA合成酶(AARS)酶从同源氨基酸和tRNA合成氨基酰基tRNA的催化方法。这种连接酶反应通过活化的腺苷酸氨基酰(aa-AMP)进行。aars的共同主题包括通过类保守序列和结构基序使用诱导拟合来驱动催化和过渡态稳定。活性位点金属离子参与氨基酸活化步骤,而氨基酸转移到tRNA通常是一个底物辅助协同机制。类之间的区别是氨基酰化的限速步骤。我们为氨基酰化催化的每个方面提供了一些例子,包括为解决AARS化学问题而开发的实验方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Putting amino acids onto tRNAs: The aminoacyl-tRNA synthetases as catalysts.

In this chapter we consider the catalytic approaches used by aminoacyl-tRNA synthetase (AARS) enzymes to synthesize aminoacyl-tRNA from cognate amino acid and tRNA. This ligase reaction proceeds through an activated aminoacyl-adenylate (aa-AMP). Common themes among AARSs include use of induced fit to drive catalysis and transition state stabilization by class-conserved sequence and structure motifs. Active site metal ions contribute to the amino acid activation step, while amino acid transfer to tRNA is generally a substrate-assisted concerted mechanism. A distinction between classes is the rate-limiting step for aminoacylation. We present some examples for each aspect of aminoacylation catalysis, including the experimental approaches developed to address questions of AARS chemistry.

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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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