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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...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Elsevier Pub. Co
2010
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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. |
format | Text |
id | pubmed-2845818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Elsevier Pub. Co |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT eswaranjeyanthy insightsintoproteinkinaseregulationandinhibitionbylargescalestructuralcomparison AT knappstefan insightsintoproteinkinaseregulationandinhibitionbylargescalestructuralcomparison |