Cargando…
The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases
Phosphorylation by kinases governs many key cellular and extracellular processes, such as transcription, cell cycle progression, differentiation, secretion and apoptosis. Unsurprisingly, tight and precise kinase regulation is a prerequisite for normal cell functioning, whereas kinase dysregulation o...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700312/ https://www.ncbi.nlm.nih.gov/pubmed/33233473 http://dx.doi.org/10.3390/ijms21228824 |
_version_ | 1783616250073579520 |
---|---|
author | Obsilova, Veronika Obsil, Tomas |
author_facet | Obsilova, Veronika Obsil, Tomas |
author_sort | Obsilova, Veronika |
collection | PubMed |
description | Phosphorylation by kinases governs many key cellular and extracellular processes, such as transcription, cell cycle progression, differentiation, secretion and apoptosis. Unsurprisingly, tight and precise kinase regulation is a prerequisite for normal cell functioning, whereas kinase dysregulation often leads to disease. Moreover, the functions of many kinases are regulated through protein–protein interactions, which in turn are mediated by phosphorylated motifs and often involve associations with the scaffolding and chaperon protein 14-3-3. Therefore, the aim of this review article is to provide an overview of the state of the art on 14-3-3-mediated kinase regulation, focusing on the most recent mechanistic insights into these important protein–protein interactions and discussing in detail both their structural aspects and functional consequences. |
format | Online Article Text |
id | pubmed-7700312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77003122020-11-30 The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases Obsilova, Veronika Obsil, Tomas Int J Mol Sci Review Phosphorylation by kinases governs many key cellular and extracellular processes, such as transcription, cell cycle progression, differentiation, secretion and apoptosis. Unsurprisingly, tight and precise kinase regulation is a prerequisite for normal cell functioning, whereas kinase dysregulation often leads to disease. Moreover, the functions of many kinases are regulated through protein–protein interactions, which in turn are mediated by phosphorylated motifs and often involve associations with the scaffolding and chaperon protein 14-3-3. Therefore, the aim of this review article is to provide an overview of the state of the art on 14-3-3-mediated kinase regulation, focusing on the most recent mechanistic insights into these important protein–protein interactions and discussing in detail both their structural aspects and functional consequences. MDPI 2020-11-21 /pmc/articles/PMC7700312/ /pubmed/33233473 http://dx.doi.org/10.3390/ijms21228824 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Obsilova, Veronika Obsil, Tomas The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title | The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title_full | The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title_fullStr | The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title_full_unstemmed | The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title_short | The 14-3-3 Proteins as Important Allosteric Regulators of Protein Kinases |
title_sort | 14-3-3 proteins as important allosteric regulators of protein kinases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700312/ https://www.ncbi.nlm.nih.gov/pubmed/33233473 http://dx.doi.org/10.3390/ijms21228824 |
work_keys_str_mv | AT obsilovaveronika the1433proteinsasimportantallostericregulatorsofproteinkinases AT obsiltomas the1433proteinsasimportantallostericregulatorsofproteinkinases AT obsilovaveronika 1433proteinsasimportantallostericregulatorsofproteinkinases AT obsiltomas 1433proteinsasimportantallostericregulatorsofproteinkinases |