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 During TNF-alpha or Fas ligand-induced apoptosis TRAF1 can b...
| Class:Id | Summation:5657939 |
|---|---|
| _displayName | During TNF-alpha or Fas ligand-induced apoptosis TRAF1 can b... |
| _timestamp | 2015-05-12 19:46:04 |
| created | [InstanceEdit:5657940] Shamovsky, V, 2014-12-16 |
| literatureReference | [LiteratureReference:5657914] Caspase-cleaved TRAF1 negatively regulates the antiapoptotic signals of TRAF2 during TNF-induced cell death [LiteratureReference:5634170] Caspase-mediated cleavage converts the tumor necrosis factor (TNF) receptor-associated factor (TRAF)-1 from a selective modulator of TNF receptor signaling to a general inhibitor of NF-kappaB activation [LiteratureReference:5634227] TRAF1 is a substrate of caspases activated during tumor necrosis factor receptor-alpha-induced apoptosis [LiteratureReference:5657941] Caspase-induced inactivation of the anti-apoptotic TRAF1 during Fas ligand-mediated apoptosis |
| modified | [InstanceEdit:5660773] Shamovsky, V, 2015-01-06 [InstanceEdit:5692530] Shamovsky, Veronica, 2015-05-12 |
| text | During TNF-alpha or Fas ligand-induced apoptosis TRAF1 can be processed into two fragments (Imler M et al. 2000; Leo E et al. 2001). Caspases-3, -6 and most efficiently caspase-8 cleave TRAF1 in vitro (Imler M et al. 2000; Leo E et al. 2001). Cleavage of TRAF1 occurs at the Asp-163 residue. A mutant TRAF1 (Asp163Ala) was not processed by either caspase (Imler M et al. 2000). The C-terminal cleavage product of TRAF1 was found to inhibit the induction of NFkB when co-expressed with NFkB inducers (such as TNFR1, DR3, TNFR2, Fas etc.) in human embryonic kidney 293 (HEK293) cells or upon treatment with TNF (Imler M et al. 2000; Henkler F et al. 2003). Furthermore, co-transfection of VSV-tagged IKKbeta and TRAF1(truncated or wild-type) into HEK293 or Jurkat T-cells followed by anti-VSV immunoprecipitation coupled with GST-IkB alpha immunocomplex kinase assays for IKK activity revealed that the caspase-generated TRAF1-fragment, but not TRAF1 itself inhibited IKK activation (Henkler F et al. 2003). |
| (summation) | [BlackBoxEvent:5634228] TRAF1 is cleaved by caspases [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by During TNF-alpha or Fas ligand-induced apoptosis TRAF1 can b... (5657939)
