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Insights into protein kinase regulation and inhibition by large scale structural comparison

Protein structure determination of soluble globular protein domains has developed into an efficient routine technology which can now be applied to generate and analyze structures of entire human protein families. In the kinase area, several kinase families still lack comprehensive structural analysi...

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Detalles Bibliográficos
Autores principales: Eswaran, Jeyanthy, Knapp, Stefan
Formato: Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845818/
https://www.ncbi.nlm.nih.gov/pubmed/19854302
http://dx.doi.org/10.1016/j.bbapap.2009.10.013
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author Eswaran, Jeyanthy
Knapp, Stefan
author_facet Eswaran, Jeyanthy
Knapp, Stefan
author_sort Eswaran, Jeyanthy
collection PubMed
description Protein structure determination of soluble globular protein domains has developed into an efficient routine technology which can now be applied to generate and analyze structures of entire human protein families. In the kinase area, several kinase families still lack comprehensive structural analysis. Nevertheless, Structural Genomics (SG) efforts contributed more than 40 kinase catalytic domain structures during the past 4 years providing a rich resource of information for large scale comparisons of kinase active sites. Moreover, many of the released structures are inhibitor complexes that offer chemical starting points for development of selective and potent inhibitors. Here we discuss the currently available structural data and strategies that can be utilized for the development of highly selective inhibitors.
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spelling pubmed-28458182010-03-31 Insights into protein kinase regulation and inhibition by large scale structural comparison Eswaran, Jeyanthy Knapp, Stefan Biochim Biophys Acta Review Protein structure determination of soluble globular protein domains has developed into an efficient routine technology which can now be applied to generate and analyze structures of entire human protein families. In the kinase area, several kinase families still lack comprehensive structural analysis. Nevertheless, Structural Genomics (SG) efforts contributed more than 40 kinase catalytic domain structures during the past 4 years providing a rich resource of information for large scale comparisons of kinase active sites. Moreover, many of the released structures are inhibitor complexes that offer chemical starting points for development of selective and potent inhibitors. Here we discuss the currently available structural data and strategies that can be utilized for the development of highly selective inhibitors. Elsevier Pub. Co 2010-03 /pmc/articles/PMC2845818/ /pubmed/19854302 http://dx.doi.org/10.1016/j.bbapap.2009.10.013 Text en © 2010 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Review
Eswaran, Jeyanthy
Knapp, Stefan
Insights into protein kinase regulation and inhibition by large scale structural comparison
title Insights into protein kinase regulation and inhibition by large scale structural comparison
title_full Insights into protein kinase regulation and inhibition by large scale structural comparison
title_fullStr Insights into protein kinase regulation and inhibition by large scale structural comparison
title_full_unstemmed Insights into protein kinase regulation and inhibition by large scale structural comparison
title_short Insights into protein kinase regulation and inhibition by large scale structural comparison
title_sort insights into protein kinase regulation and inhibition by large scale structural comparison
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845818/
https://www.ncbi.nlm.nih.gov/pubmed/19854302
http://dx.doi.org/10.1016/j.bbapap.2009.10.013
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