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Structural Aspects of LIMK Regulation and Pharmacology

Malfunction of the actin cytoskeleton is linked to numerous human diseases including neurological disorders and cancer. LIMK1 (LIM domain kinase 1) and its paralogue LIMK2 are two closely related kinases that control actin cytoskeleton dynamics. Consequently, they are potential therapeutic targets f...

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Detalles Bibliográficos
Autores principales: Chatterjee, Deep, Preuss, Franziska, Dederer, Verena, Knapp, Stefan, Mathea, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750758/
https://www.ncbi.nlm.nih.gov/pubmed/35011704
http://dx.doi.org/10.3390/cells11010142
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author Chatterjee, Deep
Preuss, Franziska
Dederer, Verena
Knapp, Stefan
Mathea, Sebastian
author_facet Chatterjee, Deep
Preuss, Franziska
Dederer, Verena
Knapp, Stefan
Mathea, Sebastian
author_sort Chatterjee, Deep
collection PubMed
description Malfunction of the actin cytoskeleton is linked to numerous human diseases including neurological disorders and cancer. LIMK1 (LIM domain kinase 1) and its paralogue LIMK2 are two closely related kinases that control actin cytoskeleton dynamics. Consequently, they are potential therapeutic targets for the treatment of such diseases. In the present review, we describe the LIMK conformational space and its dependence on ligand binding. Furthermore, we explain the unique catalytic mechanism of the kinase, shedding light on substrate recognition and how LIMK activity is regulated. The structural features are evaluated for implications on the drug discovery process. Finally, potential future directions for targeting LIMKs pharmacologically, also beyond just inhibiting the kinase domain, are discussed.
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spelling pubmed-87507582022-01-12 Structural Aspects of LIMK Regulation and Pharmacology Chatterjee, Deep Preuss, Franziska Dederer, Verena Knapp, Stefan Mathea, Sebastian Cells Review Malfunction of the actin cytoskeleton is linked to numerous human diseases including neurological disorders and cancer. LIMK1 (LIM domain kinase 1) and its paralogue LIMK2 are two closely related kinases that control actin cytoskeleton dynamics. Consequently, they are potential therapeutic targets for the treatment of such diseases. In the present review, we describe the LIMK conformational space and its dependence on ligand binding. Furthermore, we explain the unique catalytic mechanism of the kinase, shedding light on substrate recognition and how LIMK activity is regulated. The structural features are evaluated for implications on the drug discovery process. Finally, potential future directions for targeting LIMKs pharmacologically, also beyond just inhibiting the kinase domain, are discussed. MDPI 2022-01-02 /pmc/articles/PMC8750758/ /pubmed/35011704 http://dx.doi.org/10.3390/cells11010142 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
Chatterjee, Deep
Preuss, Franziska
Dederer, Verena
Knapp, Stefan
Mathea, Sebastian
Structural Aspects of LIMK Regulation and Pharmacology
title Structural Aspects of LIMK Regulation and Pharmacology
title_full Structural Aspects of LIMK Regulation and Pharmacology
title_fullStr Structural Aspects of LIMK Regulation and Pharmacology
title_full_unstemmed Structural Aspects of LIMK Regulation and Pharmacology
title_short Structural Aspects of LIMK Regulation and Pharmacology
title_sort structural aspects of limk regulation and pharmacology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750758/
https://www.ncbi.nlm.nih.gov/pubmed/35011704
http://dx.doi.org/10.3390/cells11010142
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