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 Some peptides generated by the 26S proteasome are too long t...
| Class:Id | Summation:982877 |
|---|---|
| _displayName | Some peptides generated by the 26S proteasome are too long t... |
| _timestamp | 2010-11-01 10:30:53 |
| created | [InstanceEdit:982858] Garapati, P V, 2010-10-29 |
| literatureReference | [LiteratureReference:982859] Post-proteasomal antigen processing for major histocompatibility complex class I presentation |
| modified | [InstanceEdit:983177] Jupe, S, 2010-10-29 [InstanceEdit:983290] Garapati, P V, 2010-11-01 |
| text | Some peptides generated by the 26S proteasome are too long to bind to MHC class I molecules. These N-terminal extended precursor peptides may be trimmed by cytosolic aminopeptidases, such as Tripeptidyl peptidase II (TPP2), puromycin-sensitive aminopeptidase (PSA), bleomycin hydrolase (BH), and leucine aminopeptidase (LAP). |
| (summation) | [BlackBoxEvent:983162] Trimming of N-ter extended precursor fragments by cytosolic aminopeptidases [Homo sapiens] |
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No pathways have been reviewed or authored by Some peptides generated by the 26S proteasome are too long t... (982877)
