BMPR2
Gene Ontology Biological Process
- BMP signaling pathway [IDA, IMP, ISS, TAS]
- activin receptor signaling pathway [TAS]
- anterior/posterior pattern specification [ISS]
- artery development [ISS]
- blood vessel remodeling [ISS]
- cellular response to starvation [IEP]
- chondrocyte development [IMP]
- lung alveolus development [ISS]
- lymphangiogenesis [ISS]
- lymphatic endothelial cell differentiation [ISS]
- mesoderm formation [ISS]
- negative regulation of DNA biosynthetic process [IMP]
- negative regulation of cell growth [IDA]
- negative regulation of chondrocyte proliferation [IMP]
- negative regulation of systemic arterial blood pressure [IMP]
- negative regulation of vasoconstriction [ISS]
- positive regulation of BMP signaling pathway [IMP]
- positive regulation of bone mineralization [IMP]
- positive regulation of endothelial cell migration [IMP]
- positive regulation of endothelial cell proliferation [IMP]
- positive regulation of epithelial cell migration [IDA]
- positive regulation of osteoblast differentiation [IMP]
- positive regulation of pathway-restricted SMAD protein phosphorylation [IMP]
- regulation of cell proliferation [IMP]
- regulation of lung blood pressure [IMP, ISS]
- retina vasculature development in camera-type eye [ISS]
- transcription from RNA polymerase II promoter [IMP]
- transmembrane receptor protein serine/threonine kinase signaling pathway [IDA]
- vascular endothelial growth factor receptor signaling pathway [ISS]
- venous blood vessel development [ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
BMP7
Gene Ontology Biological Process
- BMP signaling pathway [IDA]
- SMAD protein signal transduction [IDA]
- cellular response to hypoxia [ISS]
- dendrite development [TAS]
- epithelial to mesenchymal transition [TAS]
- extracellular matrix organization [TAS]
- mesenchymal cell differentiation [IDA]
- mesenchyme development [ISS]
- mesonephros development [IEP]
- metanephros development [IEP]
- monocyte aggregation [IDA]
- negative regulation of MAP kinase activity [IDA]
- negative regulation of NF-kappaB import into nucleus [ISS]
- negative regulation of NF-kappaB transcription factor activity [ISS]
- negative regulation of cell cycle [IDA]
- negative regulation of cell death [IDA]
- negative regulation of glomerular mesangial cell proliferation [IDA]
- negative regulation of mitosis [IDA]
- negative regulation of neuron differentiation [IDA]
- negative regulation of phosphorylation [IDA]
- negative regulation of striated muscle cell apoptotic process [ISS]
- negative regulation of transcription, DNA-templated [IDA]
- neuron projection morphogenesis [IDA]
- positive regulation of bone mineralization [IDA]
- positive regulation of dendrite development [IDA]
- positive regulation of heterotypic cell-cell adhesion [IDA]
- positive regulation of hyaluranon cable assembly [IDA]
- positive regulation of osteoblast differentiation [IDA]
- positive regulation of pathway-restricted SMAD protein phosphorylation [IDA, TAS]
- positive regulation of peptidyl-threonine phosphorylation [IDA]
- positive regulation of transcription, DNA-templated [IDA]
- protein localization to nucleus [IDA]
- regulation of apoptotic process [IBA]
- regulation of pathway-restricted SMAD protein phosphorylation [IDA]
- regulation of removal of superoxide radicals [ISS]
- skeletal system development [TAS]
- steroid hormone mediated signaling pathway [IMP]
- ureteric bud development [ISS]
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
Cloning and characterization of a human type II receptor for bone morphogenetic proteins.
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor beta superfamily. Several members of this family have been shown to transduce their signals through binding to type I and type II serine-(threonine) kinase receptors. Here we report the cDNA cloning and characterization of a human type II receptor for BMPs (BMPR-II), which is distantly related to DAF-4, a ... [more]
Throughput
- Low Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| BMP7 BMPR2 | 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 | 245172 |
Curated By
- BioGRID