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Small Molecule Substrate Phosphorylation Site Inhibitors of Protein Kinases: Approaches and Challenges
Author(s) -
Meghan E. Breen,
Matthew B. Soellner
Publication year - 2014
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/cb5008376
Subject(s) - kinase , phosphorylation , small molecule , drug discovery , substrate (aquarium) , biochemistry , binding site , non competitive inhibition , enzyme , in vitro , protein kinase a , chemistry , substrate level phosphorylation , biology , microbiology and biotechnology , ecology
Protein kinases are important mediators of cellular communication and attractive drug targets for many diseases. Although success has been achieved with developing ATP-competitive kinase inhibitors, the disadvantages of ATP-competitive inhibitors have led to increased interest in targeting sites outside of the ATP binding pocket. Kinase inhibitors with substrate-competitive, ATP-noncompetitive binding modes are promising due to the possibility of increased selectivity and better agreement between biochemical and in vitro potency. However, the difficulty of identifying these types of inhibitors has resulted in significantly fewer small molecule substrate phosphorylation site inhibitors being reported compared to ATP-competitive inhibitors. This review surveys reported substrate phosphorylation site inhibitors and methods that can be applied to the discovery of such inhibitors, including a discussion of the challenges inherent to these screening methods.

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