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Following Ariadne's thread: a new perspective on RBR ubiquitin ligases

Ubiquitin signaling pathways rely on E3 ligases for effecting the final transfer of ubiquitin from E2 ubiquitin conjugating enzymes to a protein target. Here we re-evaluate the hybrid RING/HECT mechanism used by the E3 family RING-between-RINGs (RBRs) to transfer ubiquitin to substrates. We place RB...

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Autores principales: Wenzel, Dawn M, Klevit, Rachel E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305615/
https://www.ncbi.nlm.nih.gov/pubmed/22420831
http://dx.doi.org/10.1186/1741-7007-10-24
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author Wenzel, Dawn M
Klevit, Rachel E
author_facet Wenzel, Dawn M
Klevit, Rachel E
author_sort Wenzel, Dawn M
collection PubMed
description Ubiquitin signaling pathways rely on E3 ligases for effecting the final transfer of ubiquitin from E2 ubiquitin conjugating enzymes to a protein target. Here we re-evaluate the hybrid RING/HECT mechanism used by the E3 family RING-between-RINGs (RBRs) to transfer ubiquitin to substrates. We place RBRs into the context of current knowledge of HECT and RING E3s. Although not as abundant as the other types of E3s (there are only slightly more than a dozen RBR E3s in the human genome), RBRs are conserved in all eukaryotes and play important roles in biology. Re-evaluation of RBR ligases as RING/HECT E3s provokes new questions and challenges the field.
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spelling pubmed-33056152012-03-16 Following Ariadne's thread: a new perspective on RBR ubiquitin ligases Wenzel, Dawn M Klevit, Rachel E BMC Biol Review Ubiquitin signaling pathways rely on E3 ligases for effecting the final transfer of ubiquitin from E2 ubiquitin conjugating enzymes to a protein target. Here we re-evaluate the hybrid RING/HECT mechanism used by the E3 family RING-between-RINGs (RBRs) to transfer ubiquitin to substrates. We place RBRs into the context of current knowledge of HECT and RING E3s. Although not as abundant as the other types of E3s (there are only slightly more than a dozen RBR E3s in the human genome), RBRs are conserved in all eukaryotes and play important roles in biology. Re-evaluation of RBR ligases as RING/HECT E3s provokes new questions and challenges the field. BioMed Central 2012-03-15 /pmc/articles/PMC3305615/ /pubmed/22420831 http://dx.doi.org/10.1186/1741-7007-10-24 Text en Copyright ©2012 Wenzel and Klevit; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Wenzel, Dawn M
Klevit, Rachel E
Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title_full Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title_fullStr Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title_full_unstemmed Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title_short Following Ariadne's thread: a new perspective on RBR ubiquitin ligases
title_sort following ariadne's thread: a new perspective on rbr ubiquitin ligases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305615/
https://www.ncbi.nlm.nih.gov/pubmed/22420831
http://dx.doi.org/10.1186/1741-7007-10-24
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