AT1G50370
Gene Ontology Molecular Function
SAL1
Gene Ontology Biological Process
- RNA catabolic process [IMP]
- abscisic acid-activated signaling pathway [IMP]
- miRNA catabolic process [IMP]
- negative regulation of signal transduction [IMP]
- negative regulation of transcription, DNA-templated [IEP]
- phosphatidylinositol-mediated signaling [TAS]
- photoperiodism, flowering [IMP]
- positive regulation of unidimensional cell growth [IMP]
- regulation of jasmonic acid biosynthetic process [IMP]
- response to cation stress [IGI]
- response to cold [IMP]
- response to freezing [IMP]
- response to light stimulus [IEP, IMP]
- response to salt stress [IMP]
- response to water deprivation [IMP]
- sulfur compound metabolic process [IGI, ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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.
Publication
A PP6-Type Phosphatase Holoenzyme Directly Regulates PIN Phosphorylation and Auxin Efflux in Arabidopsis.
The directional transport of the phytohormone auxin depends on the phosphorylation status and polar localization of PIN-FORMED (PIN) auxin efflux proteins. While PINIOD (PID) kinase is directly involved in the phosphorylation of PIN proteins, the phosphatase holoenzyme complexes that dephosphorylate PIN proteins remain elusive. Here, we demonstrate that mutations simultaneously disrupting the function of Arabidopsis thaliana FyPP1 (for Phytochrome-associated serine/threonine ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| AT1G50370 SAL1 | Affinity Capture-Western 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. | Low | - | BioGRID | - | |
| AT1G50370 SAL1 | Co-fractionation Co-fractionation Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex. | Low | - | BioGRID | - |
Curated By
- BioGRID