Query author contributions in Reactome
Reactome depends on collaboration between our curation team and outside experts to
assemble and peer-review its pathway modules. The integration of ORCID within Reactome
enables us to meet a key challenge with authoring, curating and reviewing biological
information by incentivizing and crediting the external experts that contribute their
expertise and time to the Reactome curation process. More information is available at
ORCID and Reactome.
If you have an ORCID ID that is not listed on this page, please
forward this information to us and we will update your Reactome pathway records.
Details on Person RET has been shown to bind GRB2 directly, via Tyrosine-1096 ...
| Class:Id | Summation:8854911 |
| _displayName | RET has been shown to bind GRB2 directly, via Tyrosine-1096 ... |
| _timestamp | 2016-03-17 10:25:06 |
| created | [InstanceEdit:8854904] Jupe, Steve, 2016-01-29 |
| literatureReference | [LiteratureReference:8853733] Grb2 binding to the different isoforms of Ret tyrosine kinase [LiteratureReference:8854365] Characterization of intracellular signals via tyrosine 1062 in RET activated by glial cell line-derived neurotrophic factor [LiteratureReference:8854366] Signaling complexes and protein-protein interactions involved in the activation of the Ras and phosphatidylinositol 3-kinase pathways by the c-Ret receptor tyrosine kinase [LiteratureReference:8854350] Ret receptor tyrosine kinase activates extracellular signal-regulated kinase 2 in SK-N-MC cells [LiteratureReference:8853780] Characterization of Ret-Shc-Grb2 complex induced by GDNF, MEN 2A, and MEN 2B mutations [LiteratureReference:8854387] Glial cell line-derived neurotrophic factor induces Ret-mediated lamellipodia formation [LiteratureReference:8854379] Ret-dependent and -independent mechanisms of glial cell line-derived neurotrophic factor signaling in neuronal cells [LiteratureReference:8854910] Signaling via Shc family adapter proteins |
| modified | [InstanceEdit:8854979] Jupe, Steve, 2016-01-29 [InstanceEdit:8855517] Jupe, Steve, 2016-02-04 [InstanceEdit:8855565] Jupe, Steve, 2016-02-04 [InstanceEdit:8856227] Jupe, Steve, 2016-02-09 [InstanceEdit:8857590] Jupe, Steve, 2016-02-15 [InstanceEdit:8864966] Jupe, Steve, 2016-03-17 |
| text | RET has been shown to bind GRB2 directly, via Tyrosine-1096 (Y1096) (Alberti et al. 1998, Besset et al. 2000). GRB2 is found in a complex with SOS1 in unstimulated cells (Hayashi et al. 2000).
GDNF stimulation of neuronal cells induces the assembly of a large protein complex containing RET, GRB2 and tyrosine-phosphorylated SHC1, p85 subunit of (PI3K), GAB2 (GAB1 in Hayashi et al. 2000) and Tyrosine-protein phosphatase non-receptor type 11 (PTPN11, SHP-2) (Besset et al. 2000). This suggests that at least two distinct RET-SHC1 protein complexes can assemble via phosphorylated Y1062, one involving GRB2 and SOS1 leads to activation of the RAS-RAF-ERK pathway, another involving GRB2, GAB2 and p85 leads to the PI3K-AKT pathway. This latter complex can also assemble directly onto phosphorylated Y1096 (Besset et al. 2000).
RET can activate the RAS-RAF-ERK signaling pathway (van Weering et al. 1995, Ohiwa et al. 1997, van Weering & Bos 1997, Trupp et al. 1999, Hayashi et al. 2000). RAS signaling is markedly impaired by mutations of RET Y1062 (Hayashi et al. 2000). RET RAS signaling and the effect of the Y1062 mutation are believed to be mediated by RET complexes involving GRB2:SOS1, well known as mediators of signaling to RAS in other receptor systems (Ravichandran 2001). |
| (summation) | [Reaction:8854899] 2x p-5Y-RET:GDNF:GFRA complexes bind GRB2-1:SOS1 [Homo sapiens] |
|
[Change default viewing format]
|
No pathways have been reviewed or authored by RET has been shown to bind GRB2 directly, via Tyrosine-1096 ... (8854911)