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N 端规则识别的分子原理。

The molecular principles of N-end rule recognition.

机构信息

Center for Pharmacogenetics and Department of Pharmaceutical Sciences, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Nat Struct Mol Biol. 2010 Oct;17(10):1164-5. doi: 10.1038/nsmb1010-1164.

DOI:10.1038/nsmb1010-1164
PMID:20924402
Abstract

The N-end rule pathway is a proteolytic system in which recognition components (N-recognins) recognize a set of N-terminal residues as part of degradation signals (N-degrons). Two studies in this issue report the structures of Ubr boxes, a substrate recognition domain of eukaryotic N-recognins. We discuss how eukaryotic and prokaryotic N-recognins use a similar molecular principle to recognize a different set of N-degrons.

摘要

N-端规则途径是一种蛋白水解系统,其中识别成分(N-识别蛋白)识别一组 N-末端残基作为降解信号(N-降解基)的一部分。本期的两项研究报告了真核 N-识别蛋白的底物识别结构域 Ubr 盒的结构。我们讨论了真核和原核 N-识别蛋白如何使用相似的分子原理来识别不同的 N-降解基。

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The molecular principles of N-end rule recognition.N 端规则识别的分子原理。
Nat Struct Mol Biol. 2010 Oct;17(10):1164-5. doi: 10.1038/nsmb1010-1164.
2
Structural basis of substrate recognition and specificity in the N-end rule pathway.N 端规则途径中底物识别和特异性的结构基础。
Nat Struct Mol Biol. 2010 Oct;17(10):1182-7. doi: 10.1038/nsmb.1894. Epub 2010 Sep 12.
3
Structural basis for the recognition of N-end rule substrates by the UBR box of ubiquitin ligases.泛素连接酶 UBR 盒识别 N 端规则底物的结构基础。
Nat Struct Mol Biol. 2010 Oct;17(10):1175-81. doi: 10.1038/nsmb.1907. Epub 2010 Sep 12.
4
The substrate recognition domains of the N-end rule pathway.N端规则途径的底物识别结构域。
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A family of mammalian E3 ubiquitin ligases that contain the UBR box motif and recognize N-degrons.一类包含UBR盒基序并识别N端降解子的哺乳动物E3泛素连接酶家族。
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本文引用的文献

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Structural basis of substrate recognition and specificity in the N-end rule pathway.N 端规则途径中底物识别和特异性的结构基础。
Nat Struct Mol Biol. 2010 Oct;17(10):1182-7. doi: 10.1038/nsmb.1894. Epub 2010 Sep 12.
2
Structural basis for the recognition of N-end rule substrates by the UBR box of ubiquitin ligases.泛素连接酶 UBR 盒识别 N 端规则底物的结构基础。
Nat Struct Mol Biol. 2010 Oct;17(10):1175-81. doi: 10.1038/nsmb.1907. Epub 2010 Sep 12.
3
N-terminal acetylation of cellular proteins creates specific degradation signals.
UBR4 的 UBR 盒中特定底物的识别机制研究进展。
Commun Biol. 2023 Nov 29;6(1):1214. doi: 10.1038/s42003-023-05602-7.
4
Structure of the human UBR5 E3 ubiquitin ligase.人 UBR5 E3 泛素连接酶的结构。
Structure. 2023 May 4;31(5):541-552.e4. doi: 10.1016/j.str.2023.03.010. Epub 2023 Apr 10.
5
TRIM7 Restricts Coxsackievirus and Norovirus Infection by Detecting the C-Terminal Glutamine Generated by 3C Protease Processing.TRIM7 通过检测 3C 蛋白酶加工产生的 C 末端谷氨酰胺来限制柯萨奇病毒和诺如病毒感染。
Viruses. 2022 Jul 23;14(8):1610. doi: 10.3390/v14081610.
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Chemical modulation of SQSTM1/p62-mediated xenophagy that targets a broad range of pathogenic bacteria.化学调节 SQSTM1/p62 介导的异噬作用,靶向广泛的致病菌。
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