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BCR — FES
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
-
IRef Biogrid Interaction:
BCR
—
FES
(physical association, affinity chromatography technology)
Lionberger et al., Cancer Res 2000*
-
IRef Biogrid Interaction:
BCR
—
FES
(direct interaction, pull down)
Maru et al., Mol Cell Biol 1995*
-
IRef Biogrid Interaction:
BCR
—
FES
(physical association, affinity chromatography technology)
Maru et al., Mol Cell Biol 1995*
-
IRef Hprd Interaction:
BCR
—
FES
(in vitro)
Maru et al., Mol Cell Biol 1995*, Li et al., J Biol Chem 1996*
-
IRef Hprd Interaction:
BCR
—
FES
(in vivo)
Maru et al., Mol Cell Biol 1995*, Li et al., J Biol Chem 1996*
-
IRef Ophid Interaction:
BCR
—
FES
(aggregation, interologs mapping)
Brown et al., Bioinformatics 2005
Text-mined interactions from Literome
Lionberger et al., Cancer Res 2000
(Cell Transformation, Neoplastic...) :
Phosphorylation of wild-type Fes correlated with stimulation of
Fes tyrosine kinase activity in the
presence of
Bcr-Abl
Maru et al., Mol Cell Biol 1995
(Cell Transformation, Neoplastic) :
Coexpression of
BCR with the cytoplasmic protein-tyrosine kinase encoded by the c-fes proto-oncogene in Sf-9 cells
resulted in stable
BCR-FES protein complex formation and tyrosine phosphorylation of BCR
Ernst et al., J Biol Chem 1994
:
p210Bcr/Abl and p160v-Abl
induce an increase in the tyrosine phosphorylation of
p93c-Fes ... Furthermore,
p93c-Fes phosphorylation was
increased by
p210Bcr/Abl even when coexpressed in NIH 3T3 fibroblasts
Li et al., J Biol Chem 1996
:
Mutagenesis of BCR Tyr-177 to Phe completely abolished
FES induced
BCR binding to the GRB2 SH2 domain, identifying Tyr-177 as an additional phosphorylation site for FES