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.

Rights

Research Institute