CRY1
Gene Ontology Biological Process
- DNA damage induced protein phosphorylation [ISS]
- blue light signaling pathway [NAS]
- circadian regulation of gene expression [ISS]
- entrainment of circadian clock by photoperiod [ISS]
- gluconeogenesis [ISS]
- glucose homeostasis [ISS]
- negative regulation of G-protein coupled receptor protein signaling pathway [ISS]
- negative regulation of circadian rhythm [ISS]
- negative regulation of glucocorticoid receptor signaling pathway [ISS]
- negative regulation of protein ubiquitination [ISS]
- negative regulation of transcription from RNA polymerase II promoter [IDA]
- negative regulation of transcription, DNA-templated [IDA, ISS]
- regulation of DNA damage checkpoint [ISS]
- regulation of circadian rhythm [ISS]
- response to glucagon [ISS]
Gene Ontology Molecular Function- DNA (6-4) photolyase activity [IDA]
- DNA binding [TAS]
- blue light photoreceptor activity [NAS]
- core promoter binding [ISS]
- deoxyribodipyrimidine photo-lyase activity [IDA]
- double-stranded DNA binding [IDA]
- nuclear hormone receptor binding [IPI]
- phosphatase binding [IPI]
- protein binding [IPI]
- transcription factor binding transcription factor activity [IDA]
- ubiquitin binding [ISS]
- DNA (6-4) photolyase activity [IDA]
- DNA binding [TAS]
- blue light photoreceptor activity [NAS]
- core promoter binding [ISS]
- deoxyribodipyrimidine photo-lyase activity [IDA]
- double-stranded DNA binding [IDA]
- nuclear hormone receptor binding [IPI]
- phosphatase binding [IPI]
- protein binding [IPI]
- transcription factor binding transcription factor activity [IDA]
- ubiquitin binding [ISS]
USP2
Gene Ontology Biological Process
- circadian behavior [ISS]
- circadian regulation of gene expression [ISS]
- entrainment of circadian clock by photoperiod [ISS]
- locomotor rhythm [ISS]
- negative regulation of transcription from RNA polymerase II promoter [IMP]
- positive regulation of mitotic cell cycle [IMP]
- proteasome-mediated ubiquitin-dependent protein catabolic process [IBA]
- protein deubiquitination [IDA]
- protein stabilization [IDA, IMP]
- regulation of proteasomal protein catabolic process [IBA]
Gene Ontology Molecular Function
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
USP2a deubiquitinates and stabilizes the circadian protein CRY1 in response to inflammatory signals.
The mammalian circadian clock coordinates various physiological activities with environmental cues to achieve optimal adaptation. The clock manifests oscillations of key clock proteins, which are under dynamic control at multiple post-translational levels. As a major post-translational regulator, the ubiquitination-dependent proteasome degradation system is counterbalanced by a large group of deubiquitin proteases with distinct substrate preference. Until now, whether deubiquitination by ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| USP2 CRY1 | 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 | - | |
| USP2 CRY1 | Biochemical Activity Biochemical Activity An interaction is inferred from the biochemical effect of one protein upon another, for example, GTP-GDP exchange activity or phosphorylation of a substrate by a kinase. The bait protein executes the activity on the substrate hit protein. A Modification value is recorded for interactions of this type with the possible values Phosphorylation, Ubiquitination, Sumoylation, Dephosphorylation, Methylation, Prenylation, Acetylation, Deubiquitination, Proteolytic Processing, Glucosylation, Nedd(Rub1)ylation, Deacetylation, No Modification, Demethylation. | Low | - | BioGRID | 664498 |
Curated By
- BioGRID