BAIT
ISW1
SGN2, chromatin-remodeling ATPase ISW1, L000004447, YBR245C
ATPase subunit of imitation-switch (ISWI) class chromatin remodelers; with Ioc3p forms Isw1a complex involved in repression of transcription initiation; with Ioc2p and Ioc4p forms Isw1b complex involved in regulation of transcription elongation; Isw1b recruited to ORFs by H3K36 methylation and acts with Chd1p to prevent trans-histone exchange over coding regions; Isw1p import into nucleus depends on C-terminal bipartite nuclear targeting signal KRIR X19 KKAK
GO Process (11)
GO Function (4)
GO Component (4)
Gene Ontology Biological Process
- DNA-templated transcription, elongation [IDA, IMP]
- chromatin organization involved in regulation of transcription [IMP]
- chromatin remodeling [IGI, IMP, IPI]
- heterochromatin maintenance involved in chromatin silencing [IGI, IMP]
- negative regulation of histone exchange [IMP]
- nucleosome positioning [IGI, IMP]
- positive regulation of transcription from RNA polymerase II promoter [IMP]
- regulation of chromatin organization [IMP]
- regulation of transcriptional start site selection at RNA polymerase II promoter [IGI]
- termination of RNA polymerase I transcription [IGI]
- termination of RNA polymerase II transcription [IGI]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Saccharomyces cerevisiae (S288c)
PREY
RPC40
RPC5, DNA-directed RNA polymerase core subunit RPC40, L000001690, L000002890, YPR110C
RNA polymerase subunit AC40; common to RNA polymerase I and III
GO Process (2)
GO Function (2)
GO Component (2)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
Functional organization of the yeast proteome by systematic analysis of protein complexes.
Most cellular processes are carried out by multiprotein complexes. The identification and analysis of their components provides insight into how the ensemble of expressed proteins (proteome) is organized into functional units. We used tandem-affinity purification (TAP) and mass spectrometry in a large-scale approach to characterize multiprotein complexes in Saccharomyces cerevisiae. We processed 1,739 genes, including 1,143 human orthologues of relevance ... [more]
Nature Jan. 10, 2002; 415(6868);141-7 [Pubmed: 11805826]
Throughput
- High Throughput
Curated By
- BioGRID