CSNK2A1
Gene Ontology Biological Process
- axon guidance [TAS]
- chaperone-mediated protein folding [TAS]
- mitotic cell cycle [TAS]
- mitotic spindle checkpoint [IMP]
- negative regulation of cysteine-type endopeptidase activity involved in apoptotic process [IMP]
- positive regulation of Wnt signaling pathway [IMP]
- positive regulation of cell growth [IDA]
- positive regulation of cell proliferation [IDA]
- positive regulation of protein catabolic process [IDA]
- protein phosphorylation [IDA]
- signal transduction [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
RSF1
Gene Ontology Biological Process
- CENP-A containing nucleosome assembly [TAS]
- DNA-templated transcription, initiation [IDA]
- chromatin remodeling [IDA]
- negative regulation of DNA binding [IDA]
- negative regulation of transcription, DNA-templated [IDA]
- nucleosome assembly [IDA, TAS]
- nucleosome positioning [IDA]
- positive regulation of transcription, DNA-templated [IDA]
- positive regulation of viral transcription [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- RSF complex [IPI]
- nucleoplasm [IDA, TAS]
- nucleus [IDA]
Biochemical Activity (Phosphorylation)
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.
Publication
A bead-based approach for large-scale identification of in vitro kinase substrates.
Deciphering the kinase-substrate relationship is vital for the study of phosphorylation network. The use of immobilized proteins on protein chip as the library for screening of potential kinase substrates is a tried-and-tested method. However, information on phosphorylation sites is lacking and the creation of the library with proteins of whole proteome by recombinant expression is costly and difficult. In this ... [more]
Throughput
- High Throughput
Curated By
- BioGRID