Reactome: A Curated Pathway Database
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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.

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Details on Person LRIG1 can bind the MET receptor in the absence of HGF-mediat...

Class:IdSummation:8875403
_displayNameLRIG1 can bind the MET receptor in the absence of HGF-mediat...
_timestamp2016-07-19 14:32:15
created[InstanceEdit:8875405] Orlic-Milacic, Marija, 2016-06-03
modified[InstanceEdit:8931932] Orlic-Milacic, Marija, 2016-07-19
textLRIG1 can bind the MET receptor in the absence of HGF-mediated MET activation and trigger MET downregulation in a CBL-independent manner (Shattuck et al. 2007). MET targeting by the therapeutic antibody SAIT301 leads to LRIG1-mediated MET degradation through the lysosomal route. LRIG1-mediated MET downregulation requires ubiquitination of LRIG1 by an unknown ubiquitin ligase and can be inhibited by the ubiqitin hydrolase USP8, which deubiquitinates LRIG1 (Oh et al. 2014, Lee et al. 2014). Ubiquitinated LRIG1 binds to HGS (Hrs), a protein involved in clathrin-mediated endocytosis, and LRIG1 and MET co-localize with the lysosomal marker LAMP1 (Oh et al. 2014).
(summation)[Reaction:8875374] MET binds LRIG1 [Homo sapiens]
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