This article is
- freely available
Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
School of Molecular & Cell Biology, Gatehouse 512, University of the Witwatersrand, Johannesburg, 2050, South Africa
* Author to whom correspondence should be addressed.
Received: 28 June 2012; in revised form: 11 September 2012 / Accepted: 13 September 2012 / Published: 19 September 2012
Abstract: 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.
Keywords: ubiquitin-like; autophagy; apoptosis; immune response; DWNN; SNAMA; p53; Ubls; ubiquitin-proteasome; cancer
Article StatisticsClick here to load and display the download statistics.
Notes: Multiple requests from the same IP address are counted as one view.
Cite This Article
MDPI and ACS Style
Cajee, U.-F.; Hull, R.; Ntwasa, M. Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways. Int. J. Mol. Sci. 2012, 13, 11804-11831.
Cajee U-F, Hull R, Ntwasa M. Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways. International Journal of Molecular Sciences. 2012; 13(9):11804-11831.
Cajee, Umar-Faruq; Hull, Rodney; Ntwasa, Monde. 2012. "Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways." Int. J. Mol. Sci. 13, no. 9: 11804-11831.