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

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 a...

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Detalles Bibliográficos
Autores principales: Cajee, Umar-Faruq, Hull, Rodney, Ntwasa, Monde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472776/
https://www.ncbi.nlm.nih.gov/pubmed/23109884
http://dx.doi.org/10.3390/ijms130911804
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author Cajee, Umar-Faruq
Hull, Rodney
Ntwasa, Monde
author_facet Cajee, Umar-Faruq
Hull, Rodney
Ntwasa, Monde
author_sort Cajee, Umar-Faruq
collection PubMed
description 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.
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spelling pubmed-34727762012-10-29 Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways Cajee, Umar-Faruq Hull, Rodney Ntwasa, Monde Int J Mol Sci Review 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. Molecular Diversity Preservation International (MDPI) 2012-09-19 /pmc/articles/PMC3472776/ /pubmed/23109884 http://dx.doi.org/10.3390/ijms130911804 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Cajee, Umar-Faruq
Hull, Rodney
Ntwasa, Monde
Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title_full Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title_fullStr Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title_full_unstemmed Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title_short Modification by Ubiquitin-Like Proteins: Significance in Apoptosis and Autophagy Pathways
title_sort modification by ubiquitin-like proteins: significance in apoptosis and autophagy pathways
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472776/
https://www.ncbi.nlm.nih.gov/pubmed/23109884
http://dx.doi.org/10.3390/ijms130911804
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