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
AT5G59010
Gene Ontology Cellular Component
Biochemical Activity (Phosphorylation)
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.
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 AT5G59010 | PCA 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. | Low | - | BioGRID | - |
Curated By
- BioGRID