Explaining why Gleevec is a specific and potent inhibitor of Abl kinase.
Ontology highlight
ABSTRACT: Tyrosine kinases present attractive drug targets for specific types of cancers. Gleevec, a well-known therapeutic agent against chronic myelogenous leukemia, is an effective inhibitor of Abl tyrosine kinase. However, Gleevec fails to inhibit closely homologous tyrosine kinases, such as c-Src. Because many structural features of the binding site are conserved, the molecular determinants responsible for binding specificity are not immediately apparent. Some have attributed the difference in binding specificity of Gleevec to subtle variations in ligand-protein interactions (binding affinity control), whereas others have proposed that it is the conformation of the DFG motif, in which ligand binding is only accessible to Abl and not to c-Src (conformational selection control). To address this i
SUBMITTER: Lin YL
PROVIDER: S-EPMC3562763 | biostudies-literature | 2013 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA