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FAS — SRC
Pathways - manually collected, often from reviews:
-
NCI Pathway Database FAS (CD95) signaling pathway:
FASLG/FAS (trimer)/Src/Syk complex (FAS-FASLG-SRC-SYK)
→
SYK (SYK)
(modification, collaborate)
Beier et al., J Neurosci 2005, Letellier et al., Immunity 2010
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database FAS (CD95) signaling pathway:
FASLG/FAS (trimer)/Src/Syk complex (FAS-FASLG-SRC-SYK)
→
Src (SRC)
(modification, collaborate)
Beier et al., J Neurosci 2005, Letellier et al., Immunity 2010
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database FAS (CD95) signaling pathway:
FASLG/FAS (trimer)/Src/Syk complex (FAS-FASLG-SRC-SYK)
→
FASLG/FAS (trimer) complex (FAS-FASLG)
(modification, collaborate)
Beier et al., J Neurosci 2005, Letellier et al., Immunity 2010
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database FAS (CD95) signaling pathway:
Src (SRC)
→
FASLG/FAS (trimer) complex (FAS-FASLG)
(modification, collaborate)
Beier et al., J Neurosci 2005, Letellier et al., Immunity 2010
Evidence: mutant phenotype, assay, physical interaction
-
NCI Pathway Database FAS (CD95) signaling pathway:
FASLG/FAS (trimer)/Src/Syk complex (FAS-FASLG-SRC-SYK)
→
PI3K Class IA family (PIK3CA/PIK3R1/PIK3CB/PIK3R1)
(modification, activates)
Beier et al., J Neurosci 2005, Letellier et al., Immunity 2010
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
Text-mined interactions from Literome
Li et al., Mol Cell Biol 2003
:
Consistent with the ability of CrkL to biochemically associate with Cas, we found that
Src triggers translocation of CrkL to
focal adhesions (FAs) in a manner dependent on Cas
Reinehr et al., Gastroenterology 2008
(Disease Models, Animal...) :
In quiescent HSCs,
CD95L led to a rapid phosphorylation of the epidermal growth factor receptor (EGFR), extracellular signal regulated kinase ( Erk ), and
c-Src , but not of c-Jun-N-terminal kinase and p47(phox), an activating subunit of reduced nicotinamide adenine dinucleotide phosphate oxidase