A Pharmacological Map of the PI3-K Family Defines a Role for p110α in Insulin Signaling
نویسندگان
چکیده
Zachary A. Knight, Beatriz Gonzalez, Morri E. Feldman, Eli R. Zunder, David D. Goldenberg, Olusegun Williams, Robbie Loewith, David Stokoe, Andras Balla, Balazs Toth, Tamas Balla, William A. Weiss, Roger L. Williams, and Kevan M. Shokat* Department of Cellular and Molecular Pharmacology, Howard Hughes Medical Institute Departments of Neurology and Pediatrics, Neurological Surgery and Brain Tumor Research Center Comprehensive Cancer Center University of California, San Francisco, San Francisco, CA 94143, USA MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, United Kingdom University of Geneva, Department of Molecular Biology, CH-1211 Geneva 4, Switzerland Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA Present address: Instituto de Quı́mica-Fı́sica ‘‘Rocasolano’’ (CSIC), Serrano 119, 28006 Madrid, Spain. *Contact: [email protected] DOI 10.1016/j.cell.2006.03.035
منابع مشابه
A pharmacological map of the PI3-K family defines a role for p110alpha in insulin signaling.
Phosphoinositide 3-kinases (PI3-Ks) are an important emerging class of drug targets, but the unique roles of PI3-K isoforms remain poorly defined. We describe here an approach to pharmacologically interrogate the PI3-K family. A chemically diverse panel of PI3-K inhibitors was synthesized, and their target selectivity was biochemically enumerated, revealing cryptic homologies across targets and...
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ورودعنوان ژورنال:
- Cell
دوره 125 شماره
صفحات -
تاریخ انتشار 2006