MFB1
Gene Ontology Biological Process
Gene Ontology Cellular Component
MDM30
Gene Ontology Biological Process
- SCF-dependent proteasomal ubiquitin-dependent protein catabolic process [IMP, IPI]
- chronological cell aging [IMP]
- mitochondrial fusion [IMP]
- mitochondrion organization [IMP]
- protein ubiquitination involved in ubiquitin-dependent protein catabolic process [IMP]
- proteolysis involved in cellular protein catabolic process [IDA, IMP]
- regulation of mRNA export from nucleus [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Synthetic Growth Defect
A genetic interaction is inferred when mutations in separate genes, each of which alone causes a minimal phenotype, result in a significant growth defect under a given condition when combined in the same cell.
Publication
The novel F-box protein Mfb1p regulates mitochondrial connectivity and exhibits asymmetric localization in yeast.
Although it is clear that mitochondrial morphogenesis is a complex process involving multiple proteins in eukaryotic cells, little is known about regulatory molecules that modulate mitochondrial network formation. Here, we report the identification of a new yeast mitochondrial morphology gene called MFB1 (YDR219C). MFB1 encodes an F-box protein family member, many of which function in Skp1-Cdc53/Cullin-F-box protein (SCF) ubiquitin ligase ... [more]
Throughput
- Low Throughput
Ontology Terms
- vegetative growth (APO:0000106)
- mitochondrial morphology (APO:0000055)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
MDM30 MFB1 | 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 | -0.1836 | BioGRID | 2155177 | |
MDM30 MFB1 | 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 | -4.8103 | BioGRID | 580153 |
Curated By
- BioGRID