• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向HECT型E3连接酶——来自催化、调控及抑制剂的见解

Targeting HECT-type E3 ligases - insights from catalysis, regulation and inhibitors.

作者信息

Fajner Valentina, Maspero Elena, Polo Simona

机构信息

IFOM, Fondazione Istituto FIRC di Oncologia Molecolare, Milan, Italy.

DiPO, Dipartimento di Oncologia ed Emato-Oncologia, Università degli Studi di Milano, Italy.

出版信息

FEBS Lett. 2017 Sep;591(17):2636-2647. doi: 10.1002/1873-3468.12775. Epub 2017 Aug 20.

DOI:10.1002/1873-3468.12775
PMID:28771691
Abstract

Ubiquitination plays a pivotal role in most cellular processes and is critical for protein degradation and signalling. E3 ligases are the matchmakers in the ubiquitination cascade, responsible for substrate recognition and modification with specific polyubiquitin chains. Until recently, it was not clear how the catalytic activity of E3s is modulated, but major recent studies on HECT E3 ligases is filling this void. These enzymes appear to be held in a closed, inactive conformation, which is relieved by biochemical manoeuvres unique to each member, thus ensuring exquisite regulation and specificity of the enzymes. The new advances and their significance to the function of HECT E3s are described here, with a particular focus on the Nedd4 family members.

摘要

泛素化在大多数细胞过程中起着关键作用,对蛋白质降解和信号传导至关重要。E3 连接酶是泛素化级联反应中的“媒人”,负责底物识别以及用特定的多聚泛素链进行修饰。直到最近,E3 酶的催化活性是如何被调节的仍不清楚,但近期关于 HECT E3 连接酶的主要研究正在填补这一空白。这些酶似乎以一种封闭的、无活性的构象存在,每个成员特有的生化操作可缓解这种构象,从而确保酶的精确调控和特异性。本文描述了这些新进展及其对 HECT E3 酶功能的意义,特别关注 Nedd4 家族成员。

相似文献

1
Targeting HECT-type E3 ligases - insights from catalysis, regulation and inhibitors.靶向HECT型E3连接酶——来自催化、调控及抑制剂的见解
FEBS Lett. 2017 Sep;591(17):2636-2647. doi: 10.1002/1873-3468.12775. Epub 2017 Aug 20.
2
β-Sheet Augmentation Is a Conserved Mechanism of Priming HECT E3 Ligases for Ubiquitin Ligation.β-折叠片层增强是触发 HECT E3 连接酶泛素化连接的一种保守机制。
J Mol Biol. 2018 Sep 14;430(18 Pt B):3218-3233. doi: 10.1016/j.jmb.2018.06.044. Epub 2018 Jun 28.
3
Regulating the human HECT E3 ligases.调控人类 HECT E3 连接酶。
Cell Mol Life Sci. 2018 Sep;75(17):3121-3141. doi: 10.1007/s00018-018-2848-2. Epub 2018 Jun 1.
4
Activity-based E3 ligase profiling uncovers an E3 ligase with esterification activity.基于活性的 E3 连接酶谱分析揭示了一种具有酯化活性的 E3 连接酶。
Nature. 2018 Apr;556(7701):381-385. doi: 10.1038/s41586-018-0026-1. Epub 2018 Apr 11.
5
Physiological functions of the HECT family of ubiquitin ligases.泛素连接酶HECT家族的生理功能。
Nat Rev Mol Cell Biol. 2009 Jun;10(6):398-409. doi: 10.1038/nrm2690. Epub 2009 May 13.
6
UbFluor: A Fluorescent Thioester to Monitor HECT E3 Ligase Catalysis.UbFluor:一种用于监测HECT E3连接酶催化作用的荧光硫酯。
Curr Protoc Chem Biol. 2017 Mar 2;9(1):11-37. doi: 10.1002/cpch.17.
7
A cell-based high-throughput screening method based on a ubiquitin-reference technique for identifying modulators of E3 ligases.基于泛素参考技术的细胞高通量筛选方法,用于鉴定 E3 连接酶调节剂。
J Biol Chem. 2019 Feb 22;294(8):2880-2891. doi: 10.1074/jbc.RA118.003822. Epub 2018 Dec 26.
8
Structural insights into a HECT-type E3 ligase AREL1 and its ubiquitination activities .结构解析一个 HECT 型 E3 连接酶 AREL1 及其泛素化活性。
J Biol Chem. 2019 Dec 27;294(52):19934-19949. doi: 10.1074/jbc.RA119.010327. Epub 2019 Nov 15.
9
High-Throughput Screening of HECT E3 Ubiquitin Ligases Using UbFluor.利用UbFluor对HECT E3泛素连接酶进行高通量筛选
Curr Protoc Chem Biol. 2017 Sep 14;9(3):174-195. doi: 10.1002/cpch.24.
10
The HECT family of E3 ubiquitin ligases: multiple players in cancer development.E3泛素连接酶的HECT家族:癌症发展中的多个参与者
Cancer Cell. 2008 Jul 8;14(1):10-21. doi: 10.1016/j.ccr.2008.06.001.

引用本文的文献

1
Mechanistic insights into the iron-sulfur cluster-dependent interaction of the autophagy receptor NCOA4 with the E3 ligase HERC2.自噬受体NCOA4与E3连接酶HERC2的铁硫簇依赖性相互作用的机制洞察
Proc Natl Acad Sci U S A. 2025 Jul 29;122(30):e2510269122. doi: 10.1073/pnas.2510269122. Epub 2025 Jul 24.
2
Structure-based design of potent and selective inhibitors of the HECT ligase NEDD4.基于结构的HECT连接酶NEDD4强效和选择性抑制剂的设计
Commun Chem. 2025 May 28;8(1):164. doi: 10.1038/s42004-025-01557-4.
3
Understanding ubiquitination in neurodevelopment by integrating insights across space and time.
通过整合跨空间和时间的见解来理解神经发育中的泛素化。
Nat Struct Mol Biol. 2025 Jan;32(1):14-22. doi: 10.1038/s41594-024-01422-3. Epub 2024 Dec 4.
4
Protein semisynthesis reveals plasticity in HECT E3 ubiquitin ligase mechanisms.蛋白质半合成揭示了 HECT E3 泛素连接酶机制的灵活性。
Nat Chem. 2024 Nov;16(11):1894-1905. doi: 10.1038/s41557-024-01576-z. Epub 2024 Jul 19.
5
TRAF6 Inhibitors from Marine Compound Library: Pharmacophore, Virtual Screening, Fragment Replacement, ADMET, and Molecular Dynamics.海洋化合物库中的 TRAF6 抑制剂:药效团、虚拟筛选、片段替换、ADMET 和分子动力学。
Mar Drugs. 2024 Jun 5;22(6):260. doi: 10.3390/md22060260.
6
Herpes simplex encephalitis due to a mutation in an E3 ubiquitin ligase.单纯疱疹脑炎,源于 E3 泛素连接酶的突变。
Nat Commun. 2024 May 10;15(1):3969. doi: 10.1038/s41467-024-48287-0.
7
Structural insights into the functional mechanism of the ubiquitin ligase E6AP.泛素连接酶 E6AP 的功能机制的结构见解。
Nat Commun. 2024 Apr 26;15(1):3531. doi: 10.1038/s41467-024-47586-w.
8
The R436Q missense mutation in WWP1 disrupts autoinhibition of its E3 ubiquitin ligase activity, leading to self-degradation and loss of function.WWP1 中的 R436Q 错义突变破坏了其 E3 泛素连接酶活性的自身抑制,导致自身降解和功能丧失。
In Vitro Cell Dev Biol Anim. 2024 Aug;60(7):771-780. doi: 10.1007/s11626-024-00894-3. Epub 2024 Apr 1.
9
NEDD4L in human tumors: regulatory mechanisms and dual effects on anti-tumor and pro-tumor.人类肿瘤中的NEDD4L:调控机制及其对肿瘤抑制和肿瘤促进的双重作用
Front Pharmacol. 2023 Nov 9;14:1291773. doi: 10.3389/fphar.2023.1291773. eCollection 2023.
10
Targeting E3 ubiquitin ligases and their adaptors as a therapeutic strategy for metabolic diseases.靶向 E3 泛素连接酶及其衔接子作为代谢性疾病的治疗策略。
Exp Mol Med. 2023 Oct;55(10):2097-2104. doi: 10.1038/s12276-023-01087-w. Epub 2023 Oct 2.