Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

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.

Name Email address

Details on Person TGFBR2 recruited to tight junctions after TGF-beta stimulati...

Class:IdSummation:2134531
_displayNameTGFBR2 recruited to tight junctions after TGF-beta stimulati...
_timestamp2012-04-16 16:13:18
created[InstanceEdit:2134535] Orlic-Milacic, M, 2012-02-23
literatureReference[LiteratureReference:2134511] Regulation of the polarity protein Par6 by TGFbeta receptors controls epithelial cell plasticity
modified[InstanceEdit:2160941] Orlic-Milacic, M, 2012-03-05
[InstanceEdit:2197781] Orlic-Milacic, M, 2012-04-15
[InstanceEdit:2197821] Orlic-Milacic, M, 2012-04-16
textTGFBR2 recruited to tight junctions after TGF-beta stimulation phosphorylates PARD6A on serine residue S345, and it also phosphorylates TGFBR1 (Ozdamar et al. 2005). This was inferred from experiments in which a recombinant mouse Pard6a and recombinant human TGFBR1 and TGFBR2 were used.
(summation)[Reaction:2134532] TGFBR2 phosphorylates TGFBR1 and PARD6A [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by TGFBR2 recruited to tight junctions after TGF-beta stimulati... (2134531)