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Unraveling the role of ubiquitin-conjugating enzyme 5 (UBC5) in disease pathogenesis: A comprehensive review.

Authors :
Shi, Jin-Jin
Chen, Ru-Yi
Liu, Yan-Jun
Li, Chang-Yun
Yu, Jing
Tu, Fei-Yang
Sheng, Jian-Xiang
Lu, Jian-Fei
Zhang, Le-Le
Yang, Guan-Jun
Chen, Jiong
Source :
Cellular Signalling. Dec2024, Vol. 124, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

While certain members of ubiquitin-coupled enzymes (E2s) have garnered attention as potential therapeutic targets across diverse diseases, research progress on Ubiquitin-Conjugating Enzyme 5 (UBC5)—a pivotal member of the E2s family involved in crucial cellular processes such as apoptosis, DNA repair, and signal transduction—has been relatively sluggish. Previous findings suggest that UBC5 plays a vital role in the ubiquitination of various target proteins implicated in diseases and homeostasis, particularly in various cancer types. This review comprehensively introduces the structure and biological functions of UBC5, with a specific focus on its contributions to the onset and advancement of diverse diseases. It suggests that targeting UBC5 holds promise as a therapeutic approach for disease therapy. Recent discoveries highlighting the high homology between UBC5, UBC1, and UBC4 have provided insight into the mechanism of UBC5 in protein degradation and the regulation of cellular functions. As our comprehension of the structural distinctions among UBC5 and its homologues, namely UBC1 and UBC4, advances, our understanding of UBC5's functional significance also expands. • UBC5, a ubiquitin-conjugating enzymes (E2s), affects disease progression, homeostasis, and various cancers. • This review outlines UBC5's structure, functions, and its role in disease onset and progression. • UBC5 is an appealing target for multiple disease therapeutic intervention. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08986568
Volume :
124
Database :
Academic Search Index
Journal :
Cellular Signalling
Publication Type :
Academic Journal
Accession number :
180679021
Full Text :
https://doi.org/10.1016/j.cellsig.2024.111376