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How to Inactivate Human Ubiquitin E3 Ligases by Mutation
E3 ubiquitin ligases are the ultimate enzymes involved in the transfer of ubiquitin to substrate proteins, a process that determines the fate of the modified protein. Numerous diseases are caused by defects in the ubiquitin-proteasome machinery, including when the activity of a given E3 ligase is ha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010608/ https://www.ncbi.nlm.nih.gov/pubmed/32117970 http://dx.doi.org/10.3389/fcell.2020.00039 |
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author | Garcia-Barcena, Cristina Osinalde, Nerea Ramirez, Juanma Mayor, Ugo |
author_facet | Garcia-Barcena, Cristina Osinalde, Nerea Ramirez, Juanma Mayor, Ugo |
author_sort | Garcia-Barcena, Cristina |
collection | PubMed |
description | E3 ubiquitin ligases are the ultimate enzymes involved in the transfer of ubiquitin to substrate proteins, a process that determines the fate of the modified protein. Numerous diseases are caused by defects in the ubiquitin-proteasome machinery, including when the activity of a given E3 ligase is hampered. Thus, inactivation of E3 ligases and the resulting effects at molecular or cellular level have been the focus of many studies during the last few years. For this purpose, site-specific mutation of key residues involved in either protein interaction, substrate recognition or ubiquitin transfer have been reported to successfully inactivate E3 ligases. Nevertheless, it is not always trivial to predict which mutation(s) will block the catalytic activity of a ligase. Here we review over 250 site-specific inactivating mutations that have been carried out in 120 human E3 ubiquitin ligases. We foresee that the information gathered here will be helpful for the design of future experimental strategies. |
format | Online Article Text |
id | pubmed-7010608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70106082020-02-28 How to Inactivate Human Ubiquitin E3 Ligases by Mutation Garcia-Barcena, Cristina Osinalde, Nerea Ramirez, Juanma Mayor, Ugo Front Cell Dev Biol Cell and Developmental Biology E3 ubiquitin ligases are the ultimate enzymes involved in the transfer of ubiquitin to substrate proteins, a process that determines the fate of the modified protein. Numerous diseases are caused by defects in the ubiquitin-proteasome machinery, including when the activity of a given E3 ligase is hampered. Thus, inactivation of E3 ligases and the resulting effects at molecular or cellular level have been the focus of many studies during the last few years. For this purpose, site-specific mutation of key residues involved in either protein interaction, substrate recognition or ubiquitin transfer have been reported to successfully inactivate E3 ligases. Nevertheless, it is not always trivial to predict which mutation(s) will block the catalytic activity of a ligase. Here we review over 250 site-specific inactivating mutations that have been carried out in 120 human E3 ubiquitin ligases. We foresee that the information gathered here will be helpful for the design of future experimental strategies. Frontiers Media S.A. 2020-02-04 /pmc/articles/PMC7010608/ /pubmed/32117970 http://dx.doi.org/10.3389/fcell.2020.00039 Text en Copyright © 2020 Garcia-Barcena, Osinalde, Ramirez and Mayor. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Garcia-Barcena, Cristina Osinalde, Nerea Ramirez, Juanma Mayor, Ugo How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title | How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title_full | How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title_fullStr | How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title_full_unstemmed | How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title_short | How to Inactivate Human Ubiquitin E3 Ligases by Mutation |
title_sort | how to inactivate human ubiquitin e3 ligases by mutation |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010608/ https://www.ncbi.nlm.nih.gov/pubmed/32117970 http://dx.doi.org/10.3389/fcell.2020.00039 |
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