| Literature DB >> 18633356 |
L Mario Amzel1, Chuan-Hsiang Huang, Diana Mandelker, Christoph Lengauer, Sandra B Gabelli, Bert Vogelstein.
Abstract
Class I phosphoinositide 3-kinases (PI3Ks) are lipid kinases that regulate cell growth. One of these kinases, PI3Kalpha, is frequently mutated in diverse tumour types. The recently determined structure of PI3Kalpha reveals features that distinguish this enzyme from related lipid kinases. In addition, wild-type PI3Kgamma differs from PI3Kalpha by a substitution identical to a PI3Kalpha oncogenic mutant (His1047Arg) that might explain the differences in the enzymatic activities of the normal and mutant PI3Kalpha. Comparison of the PI3K structures also identified structural features that could potentially be exploited for the design of isoform-specific inhibitors.Entities:
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Year: 2008 PMID: 18633356 PMCID: PMC2847604 DOI: 10.1038/nrc2443
Source DB: PubMed Journal: Nat Rev Cancer ISSN: 1474-175X Impact factor: 60.716