Using chemical genetics and ATP analogues to dissect protein kinase function.
Date
2007
Advisors
Journal Title
Journal ISSN
ISSN
1554-8929
Volume Title
Publisher
American Chemical Society.
Type
Article
Peer reviewed
Abstract
Protein kinases catalyze the transfer of the γ-phosphate of ATP to a protein substrate and thereby profoundly alter the properties of the phosphorylated protein. The identification of the substrates of protein kinases has proven to be a very difficult task because of the multitude of structurally related protein kinases present in cells, their apparent redundancy of function, and the lack of absolute specificity of small-molecule inhibitors. Here, we review approaches that utilize chemical genetics to determine the functions and substrates of protein kinases, focusing on the design of ATP analogues and protein kinase binding site mutants.
Description
Keywords
Chemical genetics, Protein kinase, Adenosine triphosphate (ATP), Gatekeeper residue, Phosphorylation, Protein kinase substrate
Citation
Elphick. L.M. et al. (2007) Using chemical genetics and ATP analogues to dissect protein kinase function. ACS Chemical Biology, 2007, 2 (5), pp. 299-314.