RHO1
Gene Ontology Biological Process
- actin cytoskeleton organization [IMP]
- actin cytoskeleton reorganization [IGI, IPI]
- budding cell bud growth [IGI, IMP]
- positive regulation of endocytosis [IMP]
- positive regulation of protein kinase C signaling [IDA, IGI, IMP, IPI]
- regulation of cell size [IMP]
- regulation of cell wall (1->3)-beta-D-glucan biosynthetic process [IDA, IMP]
- regulation of exocyst localization [IMP]
- regulation of fungal-type cell wall organization [IMP]
- regulation of protein localization [IMP]
- regulation of vacuole fusion, non-autophagic [IMP]
- small GTPase mediated signal transduction [IDA, IGI]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
PXL1
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Dosage Lethality
A genetic interaction is inferred when over expression or increased dosage of one gene causes lethality in a strain that is mutated or deleted for another gene.
Publication
Pxl1p, a paxillin-like protein in Saccharomyces cerevisiae, may coordinate Cdc42p and Rho1p functions during polarized growth.
Rho-family GTPases Cdc42p and Rho1p play critical roles in the budding process of the yeast Saccharomyces cerevisiae. However, it is not clear how the functions of these GTPases are coordinated temporally and spatially during this process. Based on its ability to suppress cdc42-Ts mutants when overexpressed, a novel gene PXL1 was identified. Pxl1p resembles mammalian paxillin, which is involved in ... [more]
Throughput
- Low Throughput
Ontology Terms
- inviable (APO:0000112)
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
PXL1 RHO1 | Reconstituted Complex Reconstituted Complex An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator. | Low | - | BioGRID | - |
Curated By
- BioGRID