HTT
Gene Ontology Biological Process
- Golgi organization [IMP]
- establishment of mitotic spindle orientation [IMP]
- negative regulation of extrinsic apoptotic signaling pathway [IMP]
- organ development [IBA]
- positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity [IDA]
- regulation of protein phosphatase type 2A activity [IMP]
- retrograde vesicle-mediated transport, Golgi to ER [IMP]
- vesicle transport along microtubule [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SIN3A
Gene Ontology Biological Process
- DNA replication [IMP]
- activation of innate immune response [ISO]
- aging [ISO]
- cellular protein localization [IMP]
- cellular response to glucose stimulus [IDA]
- hematopoietic progenitor cell differentiation [IMP]
- histone deacetylation [IBA]
- in utero embryonic development [IMP]
- negative regulation of apoptotic process [IMP]
- negative regulation of circadian rhythm [IMP]
- negative regulation of histone H3-K27 acetylation [ISO]
- negative regulation of protein localization to nucleus [ISO]
- negative regulation of transcription from RNA polymerase II promoter [IGI, ISO]
- negative regulation of transcription regulatory region DNA binding [ISO]
- negative regulation of transcription, DNA-templated [IDA]
- positive regulation of G2/M transition of mitotic cell cycle [IMP]
- positive regulation of chromatin silencing [ISO]
- positive regulation of defense response to virus by host [ISO]
- positive regulation of transcription from RNA polymerase II promoter [ISO]
- protein deacetylation [ISO]
- regulation of hormone levels [ISO]
- regulation of transcription from RNA polymerase II promoter in response to oxidative stress [ISO]
- regulation of transcription, DNA-templated [IMP]
- response to methylglyoxal [IDA]
- response to organonitrogen compound [ISO]
- transcription from RNA polymerase II promoter [IGI]
Gene Ontology Molecular Function- DNA binding [IDA]
- RNA binding [ISO]
- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II repressing transcription factor binding [IPI]
- RNA polymerase II transcription corepressor activity [IGI]
- chromatin binding [IDA]
- histone deacetylase activity [IBA]
- protein binding [IPI]
- protein complex binding [ISO]
- protein deacetylase activity [ISO]
- sequence-specific DNA binding transcription factor activity [IMP]
- transcription corepressor activity [IDA]
- transcription factor binding [IPI]
- transcription regulatory region sequence-specific DNA binding [IDA]
- DNA binding [IDA]
- RNA binding [ISO]
- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II repressing transcription factor binding [IPI]
- RNA polymerase II transcription corepressor activity [IGI]
- chromatin binding [IDA]
- histone deacetylase activity [IBA]
- protein binding [IPI]
- protein complex binding [ISO]
- protein deacetylase activity [ISO]
- sequence-specific DNA binding transcription factor activity [IMP]
- transcription corepressor activity [IDA]
- transcription factor binding [IPI]
- transcription regulatory region sequence-specific DNA binding [IDA]
Gene Ontology Cellular Component
Reconstituted Complex
An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.
Publication
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription.
Huntington's Disease (HD) is caused by an expansion of a polyglutamine tract within the huntingtin (htt) protein. Pathogenesis in HD appears to include the cytoplasmic cleavage of htt and release of an amino-terminal fragment capable of nuclear localization. We have investigated potential consequences to nuclear function of a pathogenic amino-terminal region of htt (httex1p) including aggregation, protein-protein interactions, and transcription. ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID