BAIT

RPP0

RPL10E, ribosomal protein P0, P0, L10E, A0, L000002669, YLR340W
Conserved ribosomal protein P0 of the ribosomal stalk; involved in interaction between translational elongation factors and the ribosome; phosphorylated on serine 302; homologous to mammalian ribosomal protein LP0 and bacterial L10
GO Process (2)
GO Function (2)
GO Component (4)
Saccharomyces cerevisiae (S288c)
PREY

TEF2

translation elongation factor EF-1 alpha, eEF1A, EF-1 alpha, L000002278, YBR118W
Translational elongation factor EF-1 alpha; also encoded by TEF1; functions in the binding reaction of aminoacyl-tRNA (AA-tRNA) to ribosomes; TEF2-RFP levels increase during replicative aging; may also have a role in tRNA re-export from the nucleus; TEF2 has a paralog, TEF1, that arose from the whole genome duplication
GO Process (2)
GO Function (3)
GO Component (2)
Saccharomyces cerevisiae (S288c)

Affinity Capture-MS

An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.

Publication

Elevated copy number of L-A virus in yeast mutant strains defective in ribosomal stalk.

Krokowski D, Tchorzewski M, Boguszewska A, McKay AR, Maslen SL, Robinson CV, Grankowski N

The eukaryotic ribosomal stalk, composed of the P-proteins, is a part of the GTPase-associated-center which is directly responsible for stimulation of translation-factor-dependent GTP hydrolysis. Here we report that yeast mutant strains lacking P1/P2-proteins show high propagation of the yeast L-A virus. Affinity-capture-MS analysis of a protein complex isolated from a yeast mutant strain lacking the P1A/P2B proteins using anti-P0 antibodies ... [more]

Biochem. Biophys. Res. Commun. Apr. 06, 2007; 355(2);575-80 [Pubmed: 17307145]

Throughput

  • Low Throughput

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
RPP0 TEF2
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-0.3176BioGRID
2003018

Curated By

  • BioGRID