Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain

p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a comple...

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Veröffentlicht in:FEBS letters 2000-03, Vol.469 (1), p.88-92
Hauptverfasser: Chow, A, Davis, A J, Gawler, D J
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description p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a complex with the C2 domain of RasGAP; these are the Ca(2+)-dependent lipid binding protein annexin VI (p70) and two previously unidentified proteins, p55 and p120. Here we provide evidence that p55 is the Src family kinase Fyn and p120 is the focal adhesion kinase family member Pyk2. In addition, in vitro binding assays indicate that Fyn, but not Pyk2 binds directly to annexin VI. Finally, co-immunoprecipitation studies in Rat-1 fibroblasts confirm that Fyn, Pyk2, annexin VI and RasGAP can form a protein complex in mammalian cells.
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subjects Animals
Annexin A6 - metabolism
Cells, Cultured
Focal Adhesion Kinase 2
Multienzyme Complexes - chemistry
Multienzyme Complexes - metabolism
p120 GTPase Activating Protein - metabolism
Precipitin Tests
Protein Binding
Protein-Tyrosine Kinases - metabolism
Proto-Oncogene Proteins - metabolism
Proto-Oncogene Proteins c-fyn
Rats
Sheep
Signal Transduction
Transfection
title Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain
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