Sanfelice, D, Koss, H, Bunney, TD et al. (4 more authors) (2018) NMR backbone assignments of the tyrosine kinase domain of human fibroblast growth factor receptor 3 in apo state and in complex with inhibitor PD173074. Biomolecular NMR Assignments, 12 (2). pp. 231-235. ISSN 1874-2718
Abstract
Fibroblast growth factors receptors (FGFR) are transmembrane protein tyrosine kinases involved in many cellular process, including growth, differentiation and angiogenesis. Dysregulation of FGFR enzymatic activity is associated with developmental disorders and cancers; therefore FGFRs have become attractive targets for drug discovery, with a number of agents in late-stage clinical trials. Here, we present the backbone resonance assignments of FGFR3 tyrosine kinase domain in the ligand-free form and in complex with the canonical FGFR kinase inhibitor PD173074. Analysis of chemical shift changes upon inhibitor binding highlights a characteristic pattern of allosteric network perturbations that is of relevance for future drug discovery activities aimed at development of conformationally-selective FGFR inhibitors.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © The Author(s) 2018. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
Keywords: | Fibroblast growth factor receptor 3; Tyrosine kinase inhibitor; NMR resonance assignment; Cancer; Angiogenesis |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) > NMR (Leeds) |
Funding Information: | Funder Grant number Wellcome Trust 109155/Z/15/Z |
Depositing User: | Symplectic Publications |
Date Deposited: | 29 Mar 2018 10:48 |
Last Modified: | 25 Jun 2023 21:17 |
Status: | Published |
Publisher: | Springer Nature |
Identification Number: | 10.1007/s12104-018-9814-7 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:129079 |
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