BAIT

GET2

HUR2, RMD7, YER083C
Subunit of the GET complex; involved in insertion of proteins into the ER membrane; required for the retrieval of HDEL proteins from the Golgi to the ER in an ERD2 dependent fashion and for meiotic nuclear division
GO Process (2)
GO Function (1)
GO Component (3)
Saccharomyces cerevisiae (S288c)
PREY

PPG1

putative serine/threonine-protein kinase PPG1, L000001470, YNR032W
Putative serine/threonine protein phosphatase; putative phosphatase of the type 2A-like phosphatase family, required for glycogen accumulation; interacts with Tap42p, which binds to and regulates other protein phosphatases
GO Process (2)
GO Function (1)
GO Component (2)

Gene Ontology Biological Process

Gene Ontology Molecular Function

Gene Ontology Cellular Component

Saccharomyces cerevisiae (S288c)

Phenotypic Suppression

A genetic interaction is inferred when mutation or over expression of one gene results in suppression of any phenotype (other than lethality/growth defect) associated with mutation or over expression of another gene.

Publication

The GET pathway serves to activate Atg32-mediated mitophagy by ER targeting of the Ppg1-Far complex.

Onishi M, Kubota M, Duan L, Tian Y, Okamoto K

Mitophagy removes defective or superfluous mitochondria via selective autophagy. In yeast, the pro-mitophagic protein Atg32 localizes to the mitochondrial surface and interacts with the scaffold protein Atg11 to promote degradation of mitochondria. Although Atg32-Atg11 interactions are thought to be stabilized by Atg32 phosphorylation, how this posttranslational modification is regulated remains obscure. Here, we show that cells lacking the guided entry ... [more]

Life Sci Alliance Apr. 01, 2023; 6(4); [Pubmed: 36697253]

Throughput

  • Low Throughput

Ontology Terms

  • phenotype: protein activity (APO:0000022)
  • phenotype: protein/peptide modification (APO:0000131)

Additional Notes

  • genetic complex
  • in get1/2 ppg1-double-null cells, Atg32 interacted with Atg11 at near WT levels

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
GET2 PPG1
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-3.0843BioGRID
325486
GET2 PPG1
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-6.4123BioGRID
900097

Curated By

  • BioGRID