Lookup NU author(s): Professor Martin Noble,
Professor Jane Endicott
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Protein kinases are targets for treatment of a number of diseases. This review focuses on kinase inhibitors that are in the clinic or in clinical trials and for which structural information is available. Structures have informed drug design and have illuminated the mechanism of inhibition. We review progress with the receptor tyrosine kinases (growth factor receptors EGFR, VEGFR, and FGFR) and nonreceptor tyrosine kinases (Bcr-Abl), where advances have been made with cancer therapeutic agents such as Herceptin and Gleevec. Among the serine-threonine kinases, p38, Rho-kinase, cyclin-dependent kinases, and Chk1 have been targeted with productive results for inflammation and cancer. Structures have provided insights into targeting the inactive or active form of the kinase, for targeting the global constellation of residues at the ATP site or less conserved additional pockets or single residues, and into targeting noncatalytic domains.
Author(s): Noble MEM; Endicott JA; Johnson LN
Publication type: Review
Publication status: Published
ISSN (print): 0036-8075
ISSN (electronic): 1095-9203
Publisher: AMER ASSOC ADVANCEMENT SCIENCE