CREB1
Gene Ontology Biological Process
- Type I pneumocyte differentiation [IMP]
- axonogenesis [IMP]
- cellular response to growth factor stimulus [IDA]
- cellular response to zinc ion [IDA]
- circadian rhythm [IDA]
- lactation [IMP]
- lung epithelium development [IMP]
- lung saccule development [IMP]
- mammary gland development [IMP]
- memory [IMP]
- negative regulation of transcription by competitive promoter binding [ISO]
- pituitary gland development [IMP]
- positive regulation of RNA polymerase II transcriptional preinitiation complex assembly [ISO]
- positive regulation of fat cell differentiation [IGI]
- positive regulation of hormone secretion [IMP]
- positive regulation of lipid biosynthetic process [IGI]
- positive regulation of multicellular organism growth [IMP]
- positive regulation of osteoclast differentiation [IDA]
- positive regulation of transcription from RNA polymerase II promoter [IDA, ISO]
- positive regulation of transcription, DNA-templated [IGI]
- positive regulation of transforming growth factor beta3 production [ISO]
- protein phosphorylation [ISO]
- protein stabilization [IMP]
- regulation of apoptotic process [ISO]
- regulation of cell size [IGI]
- regulation of circadian rhythm [ISO]
- regulation of transcription, DNA-templated [IDA]
- response to drug [IDA]
- response to glucagon [IMP]
- response to organic substance [ISO]
- secretory granule organization [IMP]
- transcription from RNA polymerase II promoter [ISO]
- transforming growth factor beta receptor signaling pathway [ISO]
Gene Ontology Molecular Function- DNA binding [IDA]
- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding [ISO]
- RNA polymerase II distal enhancer sequence-specific DNA binding [ISO]
- RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity [ISO]
- RNA polymerase II transcription factor binding transcription factor activity involved in positive regulation of transcription [ISO]
- cAMP response element binding [ISO]
- double-stranded DNA binding [ISO]
- enzyme binding [ISO]
- histone acetyltransferase binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [IDA, ISO]
- sequence-specific DNA binding transcription factor activity [IDA, ISO]
- transcription factor binding [ISO]
- transcription regulatory region DNA binding [ISO]
- DNA binding [IDA]
- RNA polymerase II activating transcription factor binding [ISO]
- RNA polymerase II core promoter proximal region sequence-specific DNA binding [ISO]
- RNA polymerase II distal enhancer sequence-specific DNA binding [ISO]
- RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity [ISO]
- RNA polymerase II transcription factor binding transcription factor activity involved in positive regulation of transcription [ISO]
- cAMP response element binding [ISO]
- double-stranded DNA binding [ISO]
- enzyme binding [ISO]
- histone acetyltransferase binding [ISO]
- protein binding [IPI]
- sequence-specific DNA binding [IDA, ISO]
- sequence-specific DNA binding transcription factor activity [IDA, ISO]
- transcription factor binding [ISO]
- transcription regulatory region DNA binding [ISO]
Gene Ontology Cellular Component
SST
Gene Ontology Biological Process
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
Characterization of a nuclear factor that enhances DNA binding activity of SSCRE-BP/PUR alpha, a single-stranded DNA binding protein.
Pur alpha has been identified as a single-stranded DNA binding protein that specifically binds to the purine-rich strand present in the DNA replication initiation zone of the human c-myc gene. We have previously demonstrated that chronic morphine treatment decreases the DNA binding activity of ssCRE-BP (single-stranded cyclic AMP response element-binding protein), which has been shown to be identical to pur ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID