BAIT
FKH1
forkhead family transcription factor FKH1, L000002607, YIL131C
Forkhead family transcription factor; minor role in expression of G2/M phase genes; negatively regulates transcription elongation; positive role in chromatin silencing at HML, HMR; facilitates clustering and activation of early-firing replication origins; binds to recombination enhancer near HML, regulates donor preference during mating-type switching; relocalizes to cytosol in response to hypoxia; FKH1 has a paralog, FKH2, that arose from the whole genome duplication
GO Process (14)
GO Function (9)
GO Component (4)
Gene Ontology Biological Process
- cellular response to methylmercury [IGI, IMP]
- chromatin remodeling [IGI, IMP]
- donor selection [IGI, IMP]
- mRNA 3'-end processing [IMP]
- mitochondrion organization [IBA]
- negative regulation of pseudohyphal growth [IGI]
- negative regulation of transcription elongation from RNA polymerase II promoter [IGI, IMP]
- negative regulation of transcription involved in G1/S transition of mitotic cell cycle [IGI]
- negative regulation of transcription involved in G2/M transition of mitotic cell cycle [IMP]
- positive regulation of DNA-dependent DNA replication initiation [IMP]
- positive regulation of chromatin silencing at silent mating-type cassette [IGI, IMP]
- positive regulation of transcription involved in G2/M transition of mitotic cell cycle [IGI]
- regulation of sequence-specific DNA binding transcription factor activity [IBA]
- termination of RNA polymerase II transcription [IGI, IMP]
Gene Ontology Molecular Function- DNA replication origin binding [IDA]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding [IDA]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA, IGI]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [IDA, IGI]
- RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity [IBA]
- centromeric DNA binding [IDA]
- double-stranded DNA binding [IBA]
- sequence-specific DNA binding [IDA]
- transcription factor binding [IBA]
- DNA replication origin binding [IDA]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding [IDA]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription [IDA, IGI]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription [IDA, IGI]
- RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity [IBA]
- centromeric DNA binding [IDA]
- double-stranded DNA binding [IBA]
- sequence-specific DNA binding [IDA]
- transcription factor binding [IBA]
Gene Ontology Cellular Component
Saccharomyces cerevisiae (S288c)
PREY
CKA2
YOR29-12, casein kinase 2 catalytic subunit CKA2, L000000344, YOR061W
Alpha' catalytic subunit of casein kinase 2 (CK2); CK2 is a Ser/Thr protein kinase with roles in cell growth and proliferation; CK2, comprised of CKA1, CKA2, CKB1 and CKB2, has many substrates including transcription factors and all RNA polymerases; protein abundance increases in response to DNA replication stress; regulates Fkh1p-mediated donor preference during mating-type switching
GO Process (7)
GO Function (1)
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
Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry.
The recent abundance of genome sequence data has brought an urgent need for systematic proteomics to decipher the encoded protein networks that dictate cellular function. To date, generation of large-scale protein-protein interaction maps has relied on the yeast two-hybrid system, which detects binary interactions through activation of reporter gene expression. With the advent of ultrasensitive mass spectrometric protein identification methods, ... [more]
Nature Jan. 10, 2002; 415(6868);180-3 [Pubmed: 11805837]
Throughput
- High Throughput
Curated By
- BioGRID