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用于调控蛋白水解的N端规则途径:原核生物和真核生物的策略

The N-end rule pathway for regulated proteolysis: prokaryotic and eukaryotic strategies.

作者信息

Mogk Axel, Schmidt Ronny, Bukau Bernd

机构信息

ZMBH, Universität Heidelberg, Im Neuenheimer Feld 282, Heidelberg D-69120, Germany.

出版信息

Trends Cell Biol. 2007 Apr;17(4):165-72. doi: 10.1016/j.tcb.2007.02.001. Epub 2007 Feb 15.

Abstract

The N-end rule states that the half-life of a protein is determined by the nature of its N-terminal residue. This fundamental principle of regulated proteolysis is conserved from bacteria to mammals. Although prokaryotes and eukaryotes employ distinct proteolytic machineries for degradation of N-end rule substrates, recent findings indicate that they share common principles of substrate recognition. In eukaryotes substrate recognition is mediated by N-recognins, a class of E3 ligases that labels N-end rule substrates via covalent linkage to ubiquitin, allowing the subsequent substrate delivery to the 26S proteasome. In bacteria, the adaptor protein ClpS exhibits homology to the substrate binding site of N-recognin. ClpS binds to the destabilizing N-termini of N-end rule substrates and directly transfers them to the ClpAP protease.

摘要

N端规则指出,蛋白质的半衰期由其N端残基的性质决定。这种蛋白质水解调控的基本原理从细菌到哺乳动物都是保守的。尽管原核生物和真核生物采用不同的蛋白水解机制来降解N端规则底物,但最近的研究结果表明,它们在底物识别方面有共同的原则。在真核生物中,底物识别由N识别蛋白介导,这是一类E3连接酶,通过与泛素的共价连接来标记N端规则底物,从而使随后的底物被递送至26S蛋白酶体。在细菌中,衔接蛋白ClpS与N识别蛋白的底物结合位点具有同源性。ClpS与N端规则底物的不稳定N端结合,并直接将它们转移至ClpAP蛋白酶。

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