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Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome

Phosphorylation facilitates the regulation of all fundamental biological processes, which has triggered extensive research of protein kinases and their roles in human health and disease. In addition to their phosphotransferase activity, certain kinases have evolved to adopt additional catalytic func...

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Detalles Bibliográficos
Autores principales: Rangwala, Aziz M., Mingione, Victoria R., Georghiou, George, Seeliger, Markus A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138534/
https://www.ncbi.nlm.nih.gov/pubmed/35625613
http://dx.doi.org/10.3390/biom12050685
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author Rangwala, Aziz M.
Mingione, Victoria R.
Georghiou, George
Seeliger, Markus A.
author_facet Rangwala, Aziz M.
Mingione, Victoria R.
Georghiou, George
Seeliger, Markus A.
author_sort Rangwala, Aziz M.
collection PubMed
description Phosphorylation facilitates the regulation of all fundamental biological processes, which has triggered extensive research of protein kinases and their roles in human health and disease. In addition to their phosphotransferase activity, certain kinases have evolved to adopt additional catalytic functions, while others have completely lost all catalytic activity. We searched the Universal Protein Resource Knowledgebase (UniProtKB) database for bifunctional protein kinases and focused on kinases that are critical for bacterial and human cellular homeostasis. These kinases engage in diverse functional roles, ranging from environmental sensing and metabolic regulation to immune-host defense and cell cycle control. Herein, we describe their dual catalytic activities and how they contribute to disease pathogenesis.
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spelling pubmed-91385342022-05-28 Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome Rangwala, Aziz M. Mingione, Victoria R. Georghiou, George Seeliger, Markus A. Biomolecules Review Phosphorylation facilitates the regulation of all fundamental biological processes, which has triggered extensive research of protein kinases and their roles in human health and disease. In addition to their phosphotransferase activity, certain kinases have evolved to adopt additional catalytic functions, while others have completely lost all catalytic activity. We searched the Universal Protein Resource Knowledgebase (UniProtKB) database for bifunctional protein kinases and focused on kinases that are critical for bacterial and human cellular homeostasis. These kinases engage in diverse functional roles, ranging from environmental sensing and metabolic regulation to immune-host defense and cell cycle control. Herein, we describe their dual catalytic activities and how they contribute to disease pathogenesis. MDPI 2022-05-11 /pmc/articles/PMC9138534/ /pubmed/35625613 http://dx.doi.org/10.3390/biom12050685 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
Rangwala, Aziz M.
Mingione, Victoria R.
Georghiou, George
Seeliger, Markus A.
Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title_full Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title_fullStr Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title_full_unstemmed Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title_short Kinases on Double Duty: A Review of UniProtKB Annotated Bifunctionality within the Kinome
title_sort kinases on double duty: a review of uniprotkb annotated bifunctionality within the kinome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138534/
https://www.ncbi.nlm.nih.gov/pubmed/35625613
http://dx.doi.org/10.3390/biom12050685
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