BAIT

RPN10

MCB1, SUN1, proteasome regulatory particle base subunit RPN10, L000003108, YHR200W
Non-ATPase base subunit of the 19S RP of the 26S proteasome; N-terminus plays a role in maintaining the structural integrity of the regulatory particle (RP); binds selectively to polyubiquitin chains; homolog of the mammalian S5a protein
GO Process (1)
GO Function (2)
GO Component (2)
Saccharomyces cerevisiae (S288c)
PREY

SPT15

BTF1, TBP1, TATA-binding protein, TBP, L000002037, YER148W
TATA-binding protein; general transcription factor that interacts with other factors to form the preinitiation complex at promoters, essential for viability
Saccharomyces cerevisiae (S288c)

Co-fractionation

Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex.

Publication

Son1p is a component of the 26S proteasome of the yeast Saccharomyces cerevisiae.

Fujimuro M, Tanaka K, Yokosawa H, Toh-e A

A son1 mutant was isolated as a mutant showing synthetic lethality with nin1-1 which is defective in the p31 component of the regulatory subunit of the yeast 26S proteasome. son1delta showed a synthetic effect with sen3delta and sun1delta, both components of the 26S proteasome, and with cdc28-1N. The 26S proteasome was partially purified from the wild type yeast. The FPLC ... [more]

FEBS Lett. Feb. 20, 1998; 423(2);149-54 [Pubmed: 9512348]

Throughput

  • Low Throughput

Related interactions

InteractionExperimental Evidence CodeDatasetThroughputScoreCurated ByNotes
SPT15 RPN10
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-0.12BioGRID
1977079
RPN10 SPT15
Positive Genetic
Positive Genetic

Mutations/deletions in separate genes, each of which alone causes a minimal phenotype, but when combined in the same cell results in a less severe fitness defect than expected under a given condition. This term is reserved for high or low throughput studies with scores.

High0.2952BioGRID
1896591

Curated By

  • BioGRID