PARP10
Gene Ontology Biological Process
- negative regulation of NF-kappaB transcription factor activity [IMP]
- negative regulation of fibroblast proliferation [IDA]
- negative regulation of gene expression [IMP]
- negative regulation of protein K63-linked ubiquitination [IMP]
- negative regulation of protein import into nucleus, translocation [IMP]
- negative regulation of viral genome replication [IMP]
- protein ADP-ribosylation [IMP]
- protein auto-ADP-ribosylation [IMP]
- protein poly-ADP-ribosylation [IDA]
- regulation of chromatin assembly [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
RNF26
Gene Ontology Molecular Function
Proximity Label-MS
An interaction is inferred when a bait-enzyme fusion protein selectively modifies a vicinal protein with a diffusible reactive product, followed by affinity capture of the modified protein and identification by mass spectrometric methods.
Publication
Comprehensive dataset of interactors for the entire PARP family using TurboID proximity labeling.
A comprehensive dataset detailing protein interactors for the PARP family has been generated using TurboID proximity labeling under standardized experimental conditions. V5-TurboID fusion constructs enabled identification of 6,314 high-confidence interacting proteins through mass spectrometry, capturing transient interactions undetectable by conventional methods. Parallel GFP-PARP localization experiments validated physiological subcellular distributions. The dataset reveals both shared and unique interactors across PARP members, ... [more]
Throughput
- High Throughput
Additional Notes
- Turbo ID
- log2FC greater than 1 and P less than 0.05
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| RNF26 PARP10 | Reconstituted Complex Reconstituted Complex An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator. | High | - | BioGRID | - |
Curated By
- BioGRID