Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2

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SEEK ID: https://publications.h-its.org/publications/1215

SEEK ID: https://publications.h-its.org/publications/1215

DOI: 10.1016/j.chembiol.2021.01.003

Research Groups: Molecular and Cellular Modeling

Publication type: Journal

Journal: Cell Chemical Biology

Citation: Cell Chemical Biology 28(5):686-698.e7

Date Published: 1st May 2021

Registered Mode: by DOI

Authors: Benedict-Tilman Berger, Marta Amaral, Daria B. Kokh, Ariane Nunes-Alves, Djordje Musil, Timo Heinrich, Martin Schröder, Rebecca Neil, Jing Wang, Iva Navratilova, Joerg Bomke, Jonathan M. Elkins, Susanne Müller, Matthias Frech, Rebecca C. Wade, Stefan Knapp

Citation
Berger, B.-T., Amaral, M., Kokh, D. B., Nunes-Alves, A., Musil, D., Heinrich, T., Schröder, M., Neil, R., Wang, J., Navratilova, I., Bomke, J., Elkins, J. M., Müller, S., Frech, M., Wade, R. C., & Knapp, S. (2021). Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2. In Cell Chemical Biology (Vol. 28, Issue 5, pp. 686–698.e7). Elsevier BV. https://doi.org/10.1016/j.chembiol.2021.01.003
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Created: 20th Feb 2021 at 18:18

Last updated: 5th Mar 2024 at 21:24

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