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Structural and Functional Insights into GID/CTLH E3 Ligase Complexes
Multi-subunit E3 ligases facilitate ubiquitin transfer by coordinating various substrate receptor subunits with a single catalytic center. Small molecules inducing targeted protein degradation have exploited such complexes, proving successful as therapeutics against previously undruggable targets. T...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180843/ https://www.ncbi.nlm.nih.gov/pubmed/35682545 http://dx.doi.org/10.3390/ijms23115863 |
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author | Maitland, Matthew E. R. Lajoie, Gilles A. Shaw, Gary S. Schild-Poulter, Caroline |
author_facet | Maitland, Matthew E. R. Lajoie, Gilles A. Shaw, Gary S. Schild-Poulter, Caroline |
author_sort | Maitland, Matthew E. R. |
collection | PubMed |
description | Multi-subunit E3 ligases facilitate ubiquitin transfer by coordinating various substrate receptor subunits with a single catalytic center. Small molecules inducing targeted protein degradation have exploited such complexes, proving successful as therapeutics against previously undruggable targets. The C-terminal to LisH (CTLH) complex, also called the glucose-induced degradation deficient (GID) complex, is a multi-subunit E3 ligase complex highly conserved from Saccharomyces cerevisiae to humans, with roles in fundamental pathways controlling homeostasis and development in several species. However, we are only beginning to understand its mechanistic basis. Here, we review the literature of the CTLH complex from all organisms and place previous findings on individual subunits into context with recent breakthroughs on its structure and function. |
format | Online Article Text |
id | pubmed-9180843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91808432022-06-10 Structural and Functional Insights into GID/CTLH E3 Ligase Complexes Maitland, Matthew E. R. Lajoie, Gilles A. Shaw, Gary S. Schild-Poulter, Caroline Int J Mol Sci Review Multi-subunit E3 ligases facilitate ubiquitin transfer by coordinating various substrate receptor subunits with a single catalytic center. Small molecules inducing targeted protein degradation have exploited such complexes, proving successful as therapeutics against previously undruggable targets. The C-terminal to LisH (CTLH) complex, also called the glucose-induced degradation deficient (GID) complex, is a multi-subunit E3 ligase complex highly conserved from Saccharomyces cerevisiae to humans, with roles in fundamental pathways controlling homeostasis and development in several species. However, we are only beginning to understand its mechanistic basis. Here, we review the literature of the CTLH complex from all organisms and place previous findings on individual subunits into context with recent breakthroughs on its structure and function. MDPI 2022-05-24 /pmc/articles/PMC9180843/ /pubmed/35682545 http://dx.doi.org/10.3390/ijms23115863 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Maitland, Matthew E. R. Lajoie, Gilles A. Shaw, Gary S. Schild-Poulter, Caroline Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title | Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title_full | Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title_fullStr | Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title_full_unstemmed | Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title_short | Structural and Functional Insights into GID/CTLH E3 Ligase Complexes |
title_sort | structural and functional insights into gid/ctlh e3 ligase complexes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180843/ https://www.ncbi.nlm.nih.gov/pubmed/35682545 http://dx.doi.org/10.3390/ijms23115863 |
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