BAIT
SERPINE2
GDN, GDNPF, PI-7, PI7, PN-1, PN1, PNI
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
GO Process (8)
GO Function (5)
GO Component (8)
Gene Ontology Biological Process
- negative regulation of blood coagulation [IC, IDA]
- negative regulation of endopeptidase activity [IBA]
- negative regulation of plasminogen activation [IMP]
- negative regulation of platelet aggregation [ISS]
- negative regulation of protein processing [IC]
- negative regulation of proteolysis [IDA]
- positive regulation of astrocyte differentiation [IDA]
- regulation of cell migration [NAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
NCBP1
CBP80, NCBP, Sto1, RP11-546O6.1
nuclear cap binding protein subunit 1, 80kDa
GO Process (20)
GO Function (3)
GO Component (7)
Gene Ontology Biological Process
- 7-methylguanosine mRNA capping [IDA, TAS]
- RNA metabolic process [TAS]
- RNA splicing [TAS]
- gene expression [TAS]
- histone mRNA metabolic process [TAS]
- mRNA 3'-end processing [TAS]
- mRNA cleavage [IDA]
- mRNA export from nucleus [IMP, TAS]
- mRNA metabolic process [TAS]
- mRNA splicing, via spliceosome [TAS]
- ncRNA metabolic process [TAS]
- nuclear-transcribed mRNA catabolic process, nonsense-mediated decay [IDA, IMP, TAS]
- positive regulation of mRNA 3'-end processing [IDA]
- positive regulation of viral transcription [TAS]
- regulation of translational initiation [IDA]
- spliceosomal snRNP assembly [TAS]
- termination of RNA polymerase II transcription [TAS]
- transcription elongation from RNA polymerase II promoter [TAS]
- transcription from RNA polymerase II promoter [TAS]
- viral process [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
Co-fractionation
Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex.
Publication
A high-throughput approach for measuring temporal changes in the interactome.
Interactomes are often measured using affinity purification-mass spectrometry (AP-MS) or yeast two-hybrid approaches, but these methods do not provide stoichiometric or temporal information. We combine quantitative proteomics and size-exclusion chromatography to map 291 coeluting complexes. This method allows mapping of an interactome to the same depth and accuracy as AP-MS with less work and without overexpression or tagging. The use ... [more]
Nat. Methods Sep. 01, 2012; 9(9);907-9 [Pubmed: 22863883]
Throughput
- High Throughput
Ontology Terms
- cell line: hela cell (BTO:0000567) [cervical adenocarcinoma (DOID:3702)]
Curated By
- BioGRID