RBR1
Gene Ontology Biological Process
- G1/S transition of mitotic cell cycle [IMP, TAS]
- asymmetric cell division [IGI]
- cell fate specification [IMP]
- double fertilization forming a zygote and endosperm [IEP]
- embryo sac development [IMP]
- generative cell differentiation [IMP]
- leaf development [IMP]
- pollen development [IMP]
- regulation of DNA endoreduplication [IMP]
- regulation of cell cycle [IMP]
- regulation of cell growth [IMP]
- regulation of gene expression by genetic imprinting [IPI]
- regulation of nuclear division [IMP]
- regulation of stem cell maintenance [IMP]
- trichome morphogenesis [IMP]
Gene Ontology Molecular Function
CDKB1;1
Gene Ontology Biological Process
Gene Ontology Molecular Function
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Targeted interactomics reveals a complex core cell cycle machinery in Arabidopsis thaliana.
Cell proliferation is the main driving force for plant growth. Although genome sequence analysis revealed a high number of cell cycle genes in plants, little is known about the molecular complexes steering cell division. In a targeted proteomics approach, we mapped the core complex machinery at the heart of the Arabidopsis thaliana cell cycle control. Besides a central regulatory network ... [more]
Throughput
- High Throughput
Related interactions
Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
---|---|---|---|---|---|---|
CDKB1;1 RBR1 | 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