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HRAS — SRC
Pathways - manually collected, often from reviews:
-
BioCarta roles of ß arrestin dependent recruitment of src kinases in gpcr signaling:
Ligand/GPCR(+)/Arrestin/(SRC/Hck/c-Fgr) complex (CCL4_EDN1__AGT_CCL11_CXCL12_F2_compound:CAS66575-29-9_compound:CAS745-65-3-ARRB1-FGR_HCK_SRC)
→
RAS (HRAS)
(modification, activates)
-
KEGG GnRH signaling pathway:
SRC
→
HRAS/KRAS/NRAS
(protein-protein, indirect effect)
-
NCI Pathway Database Trk receptor signaling mediated by PI3K and PLC-gamma:
RAS family/GTP/PI3K complex (PIK3CA-PIK3R1-HRAS_KRAS_HRAS_KRAS_NRAS)
→
Src (SRC)
(modification, activates)
Zhang et al., EMBO J 2005
Evidence: mutant phenotype, physical interaction
-
NCI Pathway Database CXCR3-mediated signaling events:
RAS family/GDP complex (HRAS_KRAS_HRAS_KRAS_NRAS)
→
Src (SRC)
(modification, collaborate)
Bonacchi et al., J Biol Chem 2001
Evidence: assay
-
NCI Pathway Database CXCR3-mediated signaling events:
Src (SRC)
→
RAS family/GTP complex (HRAS_KRAS_HRAS_KRAS_NRAS)
(modification, activates)
Bonacchi et al., J Biol Chem 2001
Evidence: assay
-
NCI Pathway Database Nongenotropic Androgen signaling:
T-DHT/AR/PELP1/Src complex (AR-PELP1-SRC)
→
HRAS/GTP complex (HRAS)
(modification, activates)
Estrada et al., Endocrinology 2003*
Evidence: mutant phenotype, assay, other species
-
NCI Pathway Database Nongenotropic Androgen signaling:
T-DHT/AR/PELP1/Src complex (AR-PELP1-SRC)
→
HRAS/GDP complex (HRAS)
(modification, activates)
Estrada et al., Endocrinology 2003*
Evidence: mutant phenotype, assay, other species
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
Text-mined interactions from Literome
Thornton et al., J Biol Chem 2003
:
We suggest that
H-Ras negatively
regulates Src phosphorylation of NR2A and retention of NR2A into the synaptic membrane leading to inhibition of NMDA receptor function
Marais et al., EMBO J 1995
:
We show that in mammalian cells activation of p74Raf-1 by oncogenic
Src requires pp60Src to be myristoylated and the ability of p74Raf-1 to interact with
p21Ras-GTP