Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways

被引:41
作者
Cajee, Umar-Faruq [1 ]
Hull, Rodney [1 ]
Ntwasa, Monde [1 ]
机构
[1] Univ Witwatersrand, Sch Mol & Cell Biol, ZA-2050 Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
ubiquitin-like; autophagy; apoptosis; immune response; DWNN; SNAMA; p53; Ubls; ubiquitin-proteasome; cancer; ENDOPLASMIC-RETICULUM; SUMO-1; MODIFICATION; E3; LIGASE; DEPENDENT ACTIVATION; CONJUGATION SYSTEM; ANTIVIRAL MOLECULE; STIMULATED GENE-15; ISG15; CONJUGATION; PROTEASOME SYSTEM; MULTIPLE-MYELOMA;
D O I
10.3390/ijms130911804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitin-like proteins (Ubls) confer diverse functions on their target proteins. The modified proteins are involved in various biological processes, including DNA replication, signal transduction, cell cycle control, embryogenesis, cytoskeletal regulation, metabolism, stress response, homeostasis and mRNA processing. Modifiers such as SUMO, ATG12, ISG15, FAT10, URM1, and UFM have been shown to modify proteins thus conferring functions related to programmed cell death, autophagy and regulation of the immune system. Putative modifiers such as Domain With No Name (DWNN) have been identified in recent times but not fully characterized. In this review, we focus on cellular processes involving human Ubls and their targets. We review current progress in targeting these modifiers for drug design strategies.
引用
收藏
页码:11804 / 11831
页数:28
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