BAIT
ADARB1
ADAR2, DRABA2, DRADA2, RED1
adenosine deaminase, RNA-specific, B1
GO Process (10)
GO Function (6)
GO Component (4)
Gene Ontology Biological Process
- RNA processing [IDA]
- adenosine to inosine editing [IDA, TAS]
- base conversion or substitution editing [IC]
- gene expression [TAS]
- mRNA modification [TAS]
- negative regulation of cell migration [IDA]
- negative regulation of cell proliferation [IDA]
- negative regulation of protein kinase activity by regulation of protein phosphorylation [IDA]
- positive regulation of viral genome replication [IMP]
- regulation of cell cycle [IDA]
Gene Ontology Molecular Function
Homo sapiens
PREY
EEF1A1
CCS-3, CCS3, EE1A1, EEF-1, EEF1A, EF-Tu, EF1A, GRAF-1EF, HNGC:16303, LENG7, PTI1, eEF1A-1, RP11-505P4.2
eukaryotic translation elongation factor 1 alpha 1
GO Process (5)
GO Function (5)
GO Component (8)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Homo sapiens
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
Unbiased Identification of trans Regulators of ADAR and A-to-I RNA Editing.
Adenosine-to-inosine RNA editing is catalyzed by adenosine deaminase acting on RNA (ADAR) enzymes that deaminate adenosine to inosine. Although many RNA editing sites are known, few trans regulators have been identified. We perform BioID followed by mass spectrometry to identify trans regulators of ADAR1 and ADAR2 in HeLa and M17 neuroblastoma cells. We identify known and novel ADAR-interacting proteins. Using ... [more]
Cell Rep May. 19, 2020; 31(7);107656 [Pubmed: 32433965]
Throughput
- High Throughput
Additional Notes
- BioID
- High confidence protein hits had fold changes of LFC > 2 in at least two biological replicates.
- M17 cells
Curated By
- BioGRID