PKN1
Gene Ontology Biological Process
Gene Ontology Molecular Function- GTP-Rho binding [IDA]
- Rac GTPase binding [IDA]
- androgen receptor binding [IDA]
- chromatin binding [IDA]
- histone binding [IDA]
- histone deacetylase binding [IDA]
- histone kinase activity (H3-T11 specific) [IDA]
- ligand-dependent nuclear receptor transcription coactivator activity [IDA, IMP]
- protein binding [IPI]
- protein kinase C binding [IPI]
- protein kinase activity [TAS]
- protein serine/threonine kinase activity [IDA]
- GTP-Rho binding [IDA]
- Rac GTPase binding [IDA]
- androgen receptor binding [IDA]
- chromatin binding [IDA]
- histone binding [IDA]
- histone deacetylase binding [IDA]
- histone kinase activity (H3-T11 specific) [IDA]
- ligand-dependent nuclear receptor transcription coactivator activity [IDA, IMP]
- protein binding [IPI]
- protein kinase C binding [IPI]
- protein kinase activity [TAS]
- protein serine/threonine kinase activity [IDA]
PLD1
Gene Ontology Biological Process
- Ras protein signal transduction [TAS]
- chemotaxis [TAS]
- glycerophospholipid biosynthetic process [TAS]
- phosphatidic acid biosynthetic process [TAS]
- phosphatidylglycerol biosynthetic process [TAS]
- phospholipid metabolic process [TAS]
- small GTPase mediated signal transduction [TAS]
- small molecule metabolic process [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Reconstituted Complex
An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator.
Publication
PKN regulates phospholipase D1 through direct interaction.
The association of phospholipase (PLD)-1 with protein kinase C-related protein kinases, PKNalpha and PKNbeta, was analyzed. PLD1 interacted with PKNalpha and PKNbeta in COS-7 cells transiently transfected with PLD1 and PKNalpha or PKNbeta expression constructs. The interactions between endogenous PLD1 and PKNalpha or PKNbeta were confirmed by co-immunoprecipitation from mammalian cells. In vitro binding studies using the deletion mutants of ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PLD1 PKN1 | 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 | - |
Curated By
- BioGRID