Journal article
Tyrosine 740 Phosphorylation of Discoidin Domain Receptor 2 by Src Stimulates Intramolecular Autophosphorylation and Shc Signaling Complex Formation*
Abstract
DDR2 is a receptor tyrosine kinase whose activating ligands are various collagens. DDR2-mediated cellular signaling has been shown to require Src activity. However, the precise mechanism underlying the Src dependence of DDR2 signaling is unknown. Here, using baculoviral co-expression of the DDR2 cytosolic domain and Src, we show that Src targets three tyrosine residues (Tyr-736, Tyr-740, and Tyr-741) in the activation loop of DDR2 for …
Authors
Yang K; Kim JH; Kim HJ; Park I-S; Kim IY; Yang B-S
Journal
Journal of Biological Chemistry, Vol. 280, No. 47, pp. 39058–39066
Publisher
Elsevier
Publication Date
November 2005
DOI
10.1074/jbc.m506921200
ISSN
0021-9258
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Adaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsBase SequenceCell LineDNA, ComplementaryDiscoidin Domain ReceptorsHumansMiceMutagenesis, Site-DirectedNIH 3T3 CellsPhosphorylationProtein Structure, TertiaryReceptor Protein-Tyrosine KinasesReceptors, MitogenRecombinant Fusion ProteinsShc Signaling Adaptor ProteinsSignal TransductionSpodopteraSrc Homology 2 Domain-Containing, Transforming Protein 1TransfectionTyrosinesrc-Family Kinases