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 IRF3 is activated through a two-step phosphorylation in the ...

Class:IdSummation:2054083
_displayNameIRF3 is activated through a two-step phosphorylation in the ...
_timestamp2012-01-12 22:39:24
created[InstanceEdit:2054082] Shamovsky, V, 2012-01-12
textIRF3 is activated through a two-step phosphorylation in the C-terminal domain mediated by TBK1 and/or IKKi, requiring Ser386 and/or Ser385- site 1; and a cluster of serine/threonine residues between Ser396 and Ser405- site 2 [Panne et al 2007]. Phosphorylated residues at site 2 (Ser396 - Ser405) alleviate autoinhibition to allow interaction with CBP (CREB-binding protein) and facilitate phosphorylation at site 1 (Ser385 or Ser386). Phosphorylation at site 1 is required for IRF3 dimerization.
(summation)[Reaction:1606327] Phosphorylation and release of IRF3 [Homo sapiens]
[Reaction:2396007] IRF3 is phosphorylated by TBK1 [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by IRF3 is activated through a two-step phosphorylation in the ... (2054083)