BRI1
Gene Ontology Biological Process
- anther wall tapetum cell differentiation [IMP]
- brassinosteroid homeostasis [IEP]
- brassinosteroid mediated signaling pathway [IEP, IMP]
- detection of brassinosteroid stimulus [IMP]
- leaf development [IMP]
- negative regulation of cell death [IMP]
- pollen exine formation [IMP]
- positive regulation of flower development [IGI]
- regulation of seedling development [IMP]
- response to UV-B [IGI]
- unidimensional cell growth [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
AT3G54030
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
BSKs are partially redundant positive regulators of brassinosteroid signaling in Arabidopsis.
Arabidopsis thaliana Brassinosteroid Signaling Kinases (BSKs) constitute a receptor-like cytoplasmic kinase subfamily (RLCK-XII) of 12 members. Previous analysis demonstrated a positive role for BSK1 and BSK3 in the initial steps of brassinosteroid (BR) signal transduction. To investigate the function of BSKs in plant growth and BR signaling, we characterized T-DNA insertion lines within 8 BSK genes (BSK1 to BSK8) and ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| BRI1 AT3G54030 | Biochemical Activity Biochemical Activity An interaction is inferred from the biochemical effect of one protein upon another, for example, GTP-GDP exchange activity or phosphorylation of a substrate by a kinase. The bait protein executes the activity on the substrate hit protein. A Modification value is recorded for interactions of this type with the possible values Phosphorylation, Ubiquitination, Sumoylation, Dephosphorylation, Methylation, Prenylation, Acetylation, Deubiquitination, Proteolytic Processing, Glucosylation, Nedd(Rub1)ylation, Deacetylation, No Modification, Demethylation. | Low | - | BioGRID | 854998 |
Curated By
- BioGRID