TED3
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
HY5
Gene Ontology Biological Process
- gibberellic acid mediated signaling pathway [IMP]
- photomorphogenesis [TAS]
- positive regulation of anthocyanin metabolic process [IMP]
- positive regulation of circadian rhythm [IMP]
- red or far-red light signaling pathway [IMP]
- regulation of photomorphogenesis [IMP]
- regulation of transcription, DNA-templated [ISS, TAS]
- response to UV-B [IEP, IGI, IMP]
- response to abscisic acid [IMP]
- response to far red light [IEP]
- response to karrikin [IEP]
- response to red light [IEP]
Gene Ontology Molecular Function
PCA
A Protein-Fragment Complementation Assay (PCA) is a protein-protein interaction assay in which a bait protein is expressed as fusion to one of the either N- or C- terminal peptide fragments of a reporter protein and prey protein is expressed as fusion to the complementary N- or C- terminal fragment of the same reporter protein. Interaction of bait and prey proteins bring together complementary fragments, which can then fold into an active reporter, e.g. the split-ubiquitin assay.
Publication
Ectopic expression of the RING domain of the Arabidopsis peroxin2 protein partially suppresses the phenotype of the photomorphogenic mutant de-etiolated1.
The Arabidopsis constitutive photomorphogenic/de-etiolated 1/FUSCA (COP/DET1/FUS) proteins repress photomorphogenesis by degrading positive regulators of photomorphogenesis, such as the transcription factor long hypocotyl5 (HY5). The gain-of-function mutant ted3, which partially suppresses the det1 mutant, contains a missense mutation of a Val-to-Met substitution before the C-terminal RING finger domain of the peroxisomal membrane protein peroxin2 (PEX2). We hypothesized that a truncated PEX2 ... [more]
Throughput
- Low Throughput
Related interactions
Curated By
- BioGRID