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• W2164631230 abstract "Activation of the mitogen-activated protein kinase pathway represented by extracellular signal-regulated kinases (ERK1/2) and activation of the upstream kinase (MEK1) are critical events for growth factor signal transduction. c-Src has been proposed as a common mediator for these signals in response to both G protein-coupled receptors (GPCRs) and tyrosine kinase-coupled receptors (TKRs). Here we show that the GPCR kinase-interacting protein 1 (GIT1) is a substrate for c-Src that associates with MEK1 in vascular smooth-muscle cells and human embryonic kidney 293 cells. GIT1 binding via coiled-coil domains and a Spa2 homology domain is required for sustained activation of MEK1-ERK1/2 after stimulation with angiotensin II and epidermal growth factor. We propose that GIT1 serves as a scaffold protein to facilitate c-Src-dependent activation of MEK1-ERK1/2 in response to both GPCRs and TKRs." @default.
• W2164631230 created "2016-06-24" @default.
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• W2164631230 date "2004-01-01" @default.
• W2164631230 modified "2023-10-03" @default.
• W2164631230 title "GIT1 Functions as a Scaffold for MEK1–Extracellular Signal-Regulated Kinase 1 and 2 Activation by Angiotensin II and Epidermal Growth Factor" @default.
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• W2164631230 doi "https://doi.org/10.1128/mcb.24.2.875-885.2004" @default.
• W2164631230 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/343801" @default.
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