CAF20
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
CIK1
Gene Ontology Biological Process
- establishment of mitotic spindle orientation [TAS]
- karyogamy involved in conjugation with cellular fusion [IMP]
- meiotic nuclear division [IDA, IMP]
- mitotic sister chromatid segregation [TAS]
- mitotic spindle organization in nucleus [TAS]
- nuclear migration involved in conjugation with cellular fusion [IMP]
- regulation of mitotic spindle organization [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-RNA
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and associated RNA species identified by Northern blot, RT-PCR, affinity labeling, sequencing, or microarray analysis.
Publication
The 4E-BP Caf20p Mediates Both eIF4E-Dependent and Independent Repression of Translation.
Translation initiation factor eIF4E mediates mRNA selection for protein synthesis via the mRNA 5'cap. A family of binding proteins, termed the 4E-BPs, interact with eIF4E to hinder ribosome recruitment. Mechanisms underlying mRNA specificity for 4E-BP control remain poorly understood. Saccharomyces cerevisiae 4E-BPs, Caf20p and Eap1p, each regulate an overlapping set of mRNAs. We undertook global approaches to identify protein and ... [more]
Throughput
- High Throughput
Additional Notes
- FDR<0.05
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
CIK1 CAF20 | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | High | -0.1894 | BioGRID | 405666 | |
CIK1 CAF20 | Negative Genetic Negative Genetic Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a more severe fitness defect or lethality under a given condition. This term is reserved for high or low throughput studies with scores. | High | -0.1517 | BioGRID | 2164478 |
Curated By
- BioGRID