PLAU
Gene Ontology Biological Process
- blood coagulation [TAS]
- chemotaxis [TAS]
- fibrinolysis [TAS]
- regulation of cell adhesion mediated by integrin [IDA]
- regulation of receptor activity [IDA]
- regulation of smooth muscle cell migration [IDA]
- regulation of smooth muscle cell-matrix adhesion [IDA]
- regulation of wound healing [IC]
- signal transduction [TAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SERPINE2
Gene Ontology Biological Process
- negative regulation of blood coagulation [IC, IDA]
- negative regulation of endopeptidase activity [IBA]
- negative regulation of plasminogen activation [IMP]
- negative regulation of platelet aggregation [ISS]
- negative regulation of protein processing [IC]
- negative regulation of proteolysis [IDA]
- positive regulation of astrocyte differentiation [IDA]
- regulation of cell migration [NAS]
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
Recycling of the urokinase receptor upon internalization of the uPA:serpin complexes.
The GPI-anchored urokinase plasminogen activator receptor (uPAR) does not internalize free urokinase (uPA) but readily internalizes and degrades uPA:serpin complexes in a process that requires the alpha2-macroglobulin receptor/low density lipoprotein receptor-related protein (alpha2MR-LRP). This process is accompanied by the internalization of uPAR which renders it resistant to phosphatidylinositol-specific phospholipase C (PI-PLC). In this paper we show that during internalization of ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PLAU SERPINE2 | Affinity Capture-MS 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. | High | 0.9999 | BioGRID | 1194512 | |
| PLAU SERPINE2 | Affinity Capture-MS 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. | High | 0.9999 | BioGRID | 2225810 | |
| SERPINE2 PLAU | Affinity Capture-MS 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. | High | 1 | BioGRID | 3157323 | |
| PLAU SERPINE2 | Affinity Capture-MS 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. | High | 0.9999 | BioGRID | 3129246 |
Curated By
- BioGRID