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The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification

We describe the assembly and annotation of a chemogenomic set of protein kinase inhibitors as an open science resource for studying kinase biology. The set only includes inhibitors that show potent kinase inhibition and a narrow spectrum of activity when screened across a large panel of kinase bioch...

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Detalles Bibliográficos
Autores principales: Wells, Carrow I., Al-Ali, Hassan, Andrews, David M., Asquith, Christopher R. M., Axtman, Alison D., Dikic, Ivan, Ebner, Daniel, Ettmayer, Peter, Fischer, Christian, Frederiksen, Mathias, Futrell, Robert E., Gray, Nathanael S., Hatch, Stephanie B., Knapp, Stefan, Lücking, Ulrich, Michaelides, Michael, Mills, Caitlin E., Müller, Susanne, Owen, Dafydd, Picado, Alfredo, Saikatendu, Kumar S., Schröder, Martin, Stolz, Alexandra, Tellechea, Mariana, Turunen, Brandon J., Vilar, Santiago, Wang, Jinhua, Zuercher, William J., Willson, Timothy M., Drewry, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826789/
https://www.ncbi.nlm.nih.gov/pubmed/33429995
http://dx.doi.org/10.3390/ijms22020566
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author Wells, Carrow I.
Al-Ali, Hassan
Andrews, David M.
Asquith, Christopher R. M.
Axtman, Alison D.
Dikic, Ivan
Ebner, Daniel
Ettmayer, Peter
Fischer, Christian
Frederiksen, Mathias
Futrell, Robert E.
Gray, Nathanael S.
Hatch, Stephanie B.
Knapp, Stefan
Lücking, Ulrich
Michaelides, Michael
Mills, Caitlin E.
Müller, Susanne
Owen, Dafydd
Picado, Alfredo
Saikatendu, Kumar S.
Schröder, Martin
Stolz, Alexandra
Tellechea, Mariana
Turunen, Brandon J.
Vilar, Santiago
Wang, Jinhua
Zuercher, William J.
Willson, Timothy M.
Drewry, David H.
author_facet Wells, Carrow I.
Al-Ali, Hassan
Andrews, David M.
Asquith, Christopher R. M.
Axtman, Alison D.
Dikic, Ivan
Ebner, Daniel
Ettmayer, Peter
Fischer, Christian
Frederiksen, Mathias
Futrell, Robert E.
Gray, Nathanael S.
Hatch, Stephanie B.
Knapp, Stefan
Lücking, Ulrich
Michaelides, Michael
Mills, Caitlin E.
Müller, Susanne
Owen, Dafydd
Picado, Alfredo
Saikatendu, Kumar S.
Schröder, Martin
Stolz, Alexandra
Tellechea, Mariana
Turunen, Brandon J.
Vilar, Santiago
Wang, Jinhua
Zuercher, William J.
Willson, Timothy M.
Drewry, David H.
author_sort Wells, Carrow I.
collection PubMed
description We describe the assembly and annotation of a chemogenomic set of protein kinase inhibitors as an open science resource for studying kinase biology. The set only includes inhibitors that show potent kinase inhibition and a narrow spectrum of activity when screened across a large panel of kinase biochemical assays. Currently, the set contains 187 inhibitors that cover 215 human kinases. The kinase chemogenomic set (KCGS), current Version 1.0, is the most highly annotated set of selective kinase inhibitors available to researchers for use in cell-based screens.
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spelling pubmed-78267892021-01-25 The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification Wells, Carrow I. Al-Ali, Hassan Andrews, David M. Asquith, Christopher R. M. Axtman, Alison D. Dikic, Ivan Ebner, Daniel Ettmayer, Peter Fischer, Christian Frederiksen, Mathias Futrell, Robert E. Gray, Nathanael S. Hatch, Stephanie B. Knapp, Stefan Lücking, Ulrich Michaelides, Michael Mills, Caitlin E. Müller, Susanne Owen, Dafydd Picado, Alfredo Saikatendu, Kumar S. Schröder, Martin Stolz, Alexandra Tellechea, Mariana Turunen, Brandon J. Vilar, Santiago Wang, Jinhua Zuercher, William J. Willson, Timothy M. Drewry, David H. Int J Mol Sci Article We describe the assembly and annotation of a chemogenomic set of protein kinase inhibitors as an open science resource for studying kinase biology. The set only includes inhibitors that show potent kinase inhibition and a narrow spectrum of activity when screened across a large panel of kinase biochemical assays. Currently, the set contains 187 inhibitors that cover 215 human kinases. The kinase chemogenomic set (KCGS), current Version 1.0, is the most highly annotated set of selective kinase inhibitors available to researchers for use in cell-based screens. MDPI 2021-01-08 /pmc/articles/PMC7826789/ /pubmed/33429995 http://dx.doi.org/10.3390/ijms22020566 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wells, Carrow I.
Al-Ali, Hassan
Andrews, David M.
Asquith, Christopher R. M.
Axtman, Alison D.
Dikic, Ivan
Ebner, Daniel
Ettmayer, Peter
Fischer, Christian
Frederiksen, Mathias
Futrell, Robert E.
Gray, Nathanael S.
Hatch, Stephanie B.
Knapp, Stefan
Lücking, Ulrich
Michaelides, Michael
Mills, Caitlin E.
Müller, Susanne
Owen, Dafydd
Picado, Alfredo
Saikatendu, Kumar S.
Schröder, Martin
Stolz, Alexandra
Tellechea, Mariana
Turunen, Brandon J.
Vilar, Santiago
Wang, Jinhua
Zuercher, William J.
Willson, Timothy M.
Drewry, David H.
The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title_full The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title_fullStr The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title_full_unstemmed The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title_short The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification
title_sort kinase chemogenomic set (kcgs): an open science resource for kinase vulnerability identification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826789/
https://www.ncbi.nlm.nih.gov/pubmed/33429995
http://dx.doi.org/10.3390/ijms22020566
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