◀ Back to HRAS
HRAS — RASGRF1
Pathways - manually collected, often from reviews:
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OpenBEL Selventa BEL large corpus:
HRAS
→
RASGRF1
(increases, RASGRF1 Activity, HRAS Activity)
Mattingly et al., J Biol Chem 1999*
Evidence: Site-directed mutagenesis replaced each of the serine residues within this region with alanine and demonstrated that serine 916 is a major site of in vivo phosphorylation of Ras-GRF1 in both COS-7 cells and NIH-3T3 fibroblasts.
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KEGG MAPK signaling pathway:
RASGRF1/RASGRF2
→
HRAS/KRAS/MRAS/NRAS/RRAS/RRAS2
(protein-protein, activation)
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NCI Pathway Database CDC42 signaling events:
RASGRF1 (RASGRF1)
→
HRAS/GTP complex (HRAS)
(modification, activates)
Arozarena et al., J Biol Chem 2000*, Arozarena et al., J Biol Chem 2001*
Evidence: assay
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NCI Pathway Database CDC42 signaling events:
RASGRF1 (RASGRF1)
→
HRAS/GDP complex (HRAS)
(modification, activates)
Arozarena et al., J Biol Chem 2000*, Arozarena et al., J Biol Chem 2001*
Evidence: assay
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NCI Pathway Database Regulation of Ras family activation:
RASGRF1 (RASGRF1)
→
HRAS/GTP complex (HRAS)
(modification, activates)
Anborgh et al., Mol Cell Biol 1999, Mattingly et al., J Biol Chem 1999*, Yang et al., J Biol Chem 2003*, Caloca et al., J Biol Chem 2003, Shou et al., Nature 1992*, Arozarena et al., Mol Cell Biol 2004*, Freedman et al., Proc Natl Acad Sci U S A 2006*, Buday et al., Biochim Biophys Acta 2008*, Calvo et al., Mol Biol Cell 2009*, Schweighoffer et al., Oncogene 1993*, Wei et al., Gene 1994*, Gotoh et al., J Biol Chem 1997*
Evidence: assay, physical interaction
-
NCI Pathway Database Regulation of Ras family activation:
RASGRF1 (RASGRF1)
→
HRAS/GDP complex (HRAS)
(modification, activates)
Anborgh et al., Mol Cell Biol 1999, Mattingly et al., J Biol Chem 1999*, Yang et al., J Biol Chem 2003*, Caloca et al., J Biol Chem 2003, Shou et al., Nature 1992*, Arozarena et al., Mol Cell Biol 2004*, Freedman et al., Proc Natl Acad Sci U S A 2006*, Buday et al., Biochim Biophys Acta 2008*, Calvo et al., Mol Biol Cell 2009*, Schweighoffer et al., Oncogene 1993*, Wei et al., Gene 1994*, Gotoh et al., J Biol Chem 1997*
Evidence: assay, physical interaction
-
NCI Pathway Database Neurotrophic factor-mediated Trk receptor signaling:
RAS family/GDP complex (HRAS_KRAS_HRAS_KRAS_NRAS)
→
RASGRF1 (RASGRF1)
(modification, collaborate)
Yang et al., Mol Biol Cell 2006
Evidence: mutant phenotype, assay, other species
-
NCI Pathway Database Neurotrophic factor-mediated Trk receptor signaling:
RASGRF1 (RASGRF1)
→
RAS family/GTP complex (HRAS_KRAS_HRAS_KRAS_NRAS)
(modification, activates)
Yang et al., Mol Biol Cell 2006
Evidence: mutant phenotype, assay, other species
-
Reactome Reaction:
HRAS
→
RASGRF1
(reaction)
Krapivinsky et al., Neuron 2003
-
WikiPathways Serotonin Receptor 2 and ELK-SRF/GATA4 signaling:
RASGRF1
→
HRAS/KRAS/NRAS
(activation)
Arozarena et al., Mol Cell Biol 2004*
-
WikiPathways p38 MAPK Signaling Pathway:
SHC1/GRB2/RASGRF1
→
HRAS
(unknown)
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
Text-mined interactions from Literome
Gotoh et al., J Biol Chem 2001
:
Here we show that whereas
Ras-GRF1 activated both
Ha-Ras and R-Ras in cells, Ras-GRF2 activated only Ha-Ras
Arozarena et al., Mol Cell Biol 2004
:
With the aid of H-Ras constructs specifically tethered to the plasma membrane, endoplasmic reticulum, and Golgi complex, we demonstrate that
RasGRF1 and RasGRF2 can
activate plasma membrane and reticular, but not Golgi associated,
H-Ras
Yang et al., Mol Biol Cell 2006
:
These results suggest that coordinated
activation of
H-Ras and Rac1 by
Ras-GRF1 may be a significant controller of neuronal cell size
Zhu et al., J Biol Chem 2007
(MAP Kinase Signaling System...) :
Experimental evidence indicated that this phenomenon was associated with destabilization and ubiquitylation of
Ras-GRF1 , a guanine nucleotide exchange factor that
activates H-Ras by facilitating the release of GDP
Jones et al., J Biol Chem 1998
:
We found that
Ras-GRF/Cdc25Mm activates
Ha-Ras , but does not activate N-Ras or K-Ras 4B, protein in vivo