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Family-wide Structural Analysis of Human Numb-Associated Protein Kinases

The highly diverse Numb-associated kinase (NAK) family has been linked to broad cellular functions including receptor-mediated endocytosis, Notch pathway modulation, osteoblast differentiation, and dendrite morphogenesis. Consequently, NAK kinases play a key role in a diverse range of diseases from...

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Autores principales: Sorrell, Fiona J., Szklarz, Marta, Abdul Azeez, Kamal R., Elkins, Jon M., Knapp, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780864/
https://www.ncbi.nlm.nih.gov/pubmed/26853940
http://dx.doi.org/10.1016/j.str.2015.12.015
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author Sorrell, Fiona J.
Szklarz, Marta
Abdul Azeez, Kamal R.
Elkins, Jon M.
Knapp, Stefan
author_facet Sorrell, Fiona J.
Szklarz, Marta
Abdul Azeez, Kamal R.
Elkins, Jon M.
Knapp, Stefan
author_sort Sorrell, Fiona J.
collection PubMed
description The highly diverse Numb-associated kinase (NAK) family has been linked to broad cellular functions including receptor-mediated endocytosis, Notch pathway modulation, osteoblast differentiation, and dendrite morphogenesis. Consequently, NAK kinases play a key role in a diverse range of diseases from Parkinson's and prostate cancer to HIV. Due to the plasticity of this kinase family, NAK kinases are often inhibited by approved or investigational drugs and have been associated with side effects, but they are also potential drug targets. The presence of cysteine residues in some NAK family members provides the possibility for selective targeting via covalent inhibition. Here we report the first high-resolution structures of kinases AAK1 and BIKE in complex with two drug candidates. The presented data allow a comprehensive structural characterization of the NAK kinase family and provide the basis for rational design of selective NAK inhibitors.
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spelling pubmed-47808642016-03-17 Family-wide Structural Analysis of Human Numb-Associated Protein Kinases Sorrell, Fiona J. Szklarz, Marta Abdul Azeez, Kamal R. Elkins, Jon M. Knapp, Stefan Structure Article The highly diverse Numb-associated kinase (NAK) family has been linked to broad cellular functions including receptor-mediated endocytosis, Notch pathway modulation, osteoblast differentiation, and dendrite morphogenesis. Consequently, NAK kinases play a key role in a diverse range of diseases from Parkinson's and prostate cancer to HIV. Due to the plasticity of this kinase family, NAK kinases are often inhibited by approved or investigational drugs and have been associated with side effects, but they are also potential drug targets. The presence of cysteine residues in some NAK family members provides the possibility for selective targeting via covalent inhibition. Here we report the first high-resolution structures of kinases AAK1 and BIKE in complex with two drug candidates. The presented data allow a comprehensive structural characterization of the NAK kinase family and provide the basis for rational design of selective NAK inhibitors. Cell Press 2016-03-01 /pmc/articles/PMC4780864/ /pubmed/26853940 http://dx.doi.org/10.1016/j.str.2015.12.015 Text en © 2016 The Authors 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
Sorrell, Fiona J.
Szklarz, Marta
Abdul Azeez, Kamal R.
Elkins, Jon M.
Knapp, Stefan
Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title_full Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title_fullStr Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title_full_unstemmed Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title_short Family-wide Structural Analysis of Human Numb-Associated Protein Kinases
title_sort family-wide structural analysis of human numb-associated protein kinases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780864/
https://www.ncbi.nlm.nih.gov/pubmed/26853940
http://dx.doi.org/10.1016/j.str.2015.12.015
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