SYP121
Gene Ontology Biological Process
- defense response [TAS]
- defense response to fungus [IGI]
- intracellular protein transport [TAS]
- jasmonic acid mediated signaling pathway [IGI]
- maintenance of protein location in plasma membrane [IMP]
- membrane fusion [TAS]
- negative regulation of cellular defense response [IGI]
- negative regulation of defense response [IMP]
- negative regulation of programmed cell death [IGI]
- protein targeting to membrane [IDA]
- protein targeting to plasma membrane [IMP]
- regulation of plant-type hypersensitive response [IGI]
- regulation of stomatal movement [IMP]
- response to abscisic acid [IEP]
- response to fungus [IMP]
- salicylic acid mediated signaling pathway [IGI]
- transpiration [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
KAT3
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Affinity Capture-Western
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 identified by Western blot with a specific polyclonal antibody or second epitope tag. This category is also used if an interacting protein is visualized directly by dye stain or radioactivity. Note that this differs from any co-purification experiment involving affinity capture in that the co-purification experiment involves at least one extra purification step to get rid of potential contaminating proteins.
Publication
A tripartite SNARE-K+ channel complex mediates in channel-dependent K+ nutrition in Arabidopsis.
A few membrane vesicle trafficking (SNARE) proteins in plants are associated with signaling and transmembrane ion transport, including control of plasma membrane ion channels. Vesicle traffic contributes to the population of ion channels at the plasma membrane. Nonetheless, it is unclear whether these SNAREs also interact directly to affect channel gating and, if so, what functional impact this might have ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| KAT3 SYP121 | 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 | - | |
| KAT3 SYP121 | Two-hybrid Two-hybrid Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation. | Low | - | BioGRID | - | |
| KAT3 SYP121 | Two-hybrid Two-hybrid Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation. | Low | - | BioGRID | - |
Curated By
- BioGRID