TCEB1
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SOCS1
Gene Ontology Biological Process
- JAK-STAT cascade [IDA]
- cellular response to amino acid stimulus [IDA]
- cytokine-mediated signaling pathway [IDA, IMP]
- fat cell differentiation [IMP]
- negative regulation of JAK-STAT cascade [IMP]
- negative regulation of catalytic activity [IDA]
- negative regulation of insulin receptor signaling pathway [IDA]
- negative regulation of protein kinase activity [IBA]
- negative regulation of tyrosine phosphorylation of Stat3 protein [IDA]
- regulation of JAK-STAT cascade [IMP]
- regulation of activation of JAK2 kinase activity [IMP]
- regulation of cytokine secretion [IMP]
- regulation of protein phosphorylation [IDA]
- regulation of tyrosine phosphorylation of Stat1 protein [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-Western
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.
Publication
v-Abl signaling disrupts SOCS-1 function in transformed pre-B cells.
The v-Abl oncogene activates Jak-Stat signaling during transformation of pre-B cells in mice. Disrupting Jak activation by deleting the Jak binding domain of v-Abl or by expressing a dominant-negative Jak1 decreases v-Abl transformation efficiency. As SOCS-1 is a known potent inhibitor of Jak kinases, the mechanism by which v-Abl bypasses SOCS-1 regulation to constitutively activate Jak kinases was investigated. SOCS-1 ... [more]
Throughput
- Low Throughput
Additional Notes
- Phosphorylation of SOCS-1 on nontyrosine residues;v-Abl-dependent phosphorylation of SOCS-1 disrupts its interaction with Elongin C
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| SOCS1 TCEB1 | Affinity Capture-Western Affinity Capture-Western An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins. | Low | - | BioGRID | - | |
| SOCS1 TCEB1 | Reconstituted Complex Reconstituted Complex An interaction is detected between purified proteins in vitro. | Low | - | BioGRID | - |
Curated By
- BioGRID