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KInhibition: A Kinase Inhibitor Selection Portal

Protein kinases constitute a large class of signaling molecules frequently targeted in research and clinical uses. However, kinase inhibitors are notoriously non-specific, making it difficult to select an appropriate inhibitor for a given kinase. Available data from large-scale kinase inhibitor scre...

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Detalles Bibliográficos
Autores principales: Bello, Thomas, Gujral, Taranjit S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170255/
https://www.ncbi.nlm.nih.gov/pubmed/30273912
http://dx.doi.org/10.1016/j.isci.2018.09.009
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author Bello, Thomas
Gujral, Taranjit S.
author_facet Bello, Thomas
Gujral, Taranjit S.
author_sort Bello, Thomas
collection PubMed
description Protein kinases constitute a large class of signaling molecules frequently targeted in research and clinical uses. However, kinase inhibitors are notoriously non-specific, making it difficult to select an appropriate inhibitor for a given kinase. Available data from large-scale kinase inhibitor screens are often difficult to query. Here, we present KInhibition (https://kinhibition.fredhutch.org), an online portal that allows users to search publicly available datasets to find selective inhibitors for a chosen kinase or group of kinases. Compounds are sorted by a KInhibition Selectivity Score, calculated based on compounds' activity against the selected kinase(s) versus activity against all other kinases for which that compound has been profiled. The current version allows users to query four datasets, with a framework that can easily accommodate additional datasets. KInhibition represents a powerful platform through which researchers from broad areas of biology, chemistry, and pharmacology can easily interrogate large datasets to help guide their selection of kinase inhibitors.
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spelling pubmed-61702552018-10-05 KInhibition: A Kinase Inhibitor Selection Portal Bello, Thomas Gujral, Taranjit S. iScience Article Protein kinases constitute a large class of signaling molecules frequently targeted in research and clinical uses. However, kinase inhibitors are notoriously non-specific, making it difficult to select an appropriate inhibitor for a given kinase. Available data from large-scale kinase inhibitor screens are often difficult to query. Here, we present KInhibition (https://kinhibition.fredhutch.org), an online portal that allows users to search publicly available datasets to find selective inhibitors for a chosen kinase or group of kinases. Compounds are sorted by a KInhibition Selectivity Score, calculated based on compounds' activity against the selected kinase(s) versus activity against all other kinases for which that compound has been profiled. The current version allows users to query four datasets, with a framework that can easily accommodate additional datasets. KInhibition represents a powerful platform through which researchers from broad areas of biology, chemistry, and pharmacology can easily interrogate large datasets to help guide their selection of kinase inhibitors. Elsevier 2018-09-18 /pmc/articles/PMC6170255/ /pubmed/30273912 http://dx.doi.org/10.1016/j.isci.2018.09.009 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bello, Thomas
Gujral, Taranjit S.
KInhibition: A Kinase Inhibitor Selection Portal
title KInhibition: A Kinase Inhibitor Selection Portal
title_full KInhibition: A Kinase Inhibitor Selection Portal
title_fullStr KInhibition: A Kinase Inhibitor Selection Portal
title_full_unstemmed KInhibition: A Kinase Inhibitor Selection Portal
title_short KInhibition: A Kinase Inhibitor Selection Portal
title_sort kinhibition: a kinase inhibitor selection portal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170255/
https://www.ncbi.nlm.nih.gov/pubmed/30273912
http://dx.doi.org/10.1016/j.isci.2018.09.009
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