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Chem Biol. 2004 May;11(5):691-701.

Characterization of a conserved structural determinant controlling protein kinase sensitivity to selective inhibitors.

Author information

1
Axxima Pharmaceuticals AG, Max-Lebsche-Platz 32, 81377 Munich, Germany.

Abstract

Some protein kinases are known to acquire resistance to selective small molecule inhibitors upon mutation of a conserved threonine at the ATP binding site to a larger residue. Here, we performed a comprehensive mutational analysis of this structural element and determined the cellular sensitivities of several disease-relevant tyrosine kinases against various inhibitors. Mutant kinases possessing a larger side chain at the critical site showed resistance to most compounds tested, such as ZD1839, PP1, AG1296, STI571, and a pyrido[2,3-d]pyrimidine inhibitor. In contrast, indolinones affected both wild-type and mutant kinases with similar potencies. Resistant mutants were established for pharmacological analysis of betaPDGF receptor-mediated signaling and allowed the generation of a drug-inducible system of cellular Src kinase activity. Our data establish a conserved structural determinant of protein kinase sensitivity relevant for both signal transduction research and drug development.

PMID:
15157880
DOI:
10.1016/j.chembiol.2004.02.029
[Indexed for MEDLINE]
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