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Updated: Jun 19, 2026

Identification of Kinase-substrate Pairs Using High Throughput Screening
Published on: August 29, 2015
Insights into protein kinase regulation and inhibition by large scale structural comparison
Jeyanthy Eswaran1, Stefan Knapp
1Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford Old Road Campus Building, Oxford OX3 7DQ, UK. jeyanthy.eswaran@sgc.ox.ac.uk
Abstract:
Protein structure determination of soluble globular protein domains has developed into an efficient routine technology which can now be applied to generate and analyze structures of entire human protein families. In the kinase area, several kinase families still lack comprehensive structural analysis. Nevertheless, Structural Genomics (SG) efforts contributed more than 40 kinase catalytic domain structures during the past 4 years providing a rich resource of information for large scale comparisons of kinase active sites. Moreover, many of the released structures are inhibitor complexes that offer chemical starting points for development of selective and potent inhibitors. Here we discuss the currently available structural data and strategies that can be utilized for the development of highly selective inhibitors.
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