OPRD1
Gene Ontology Biological Process
- G-protein coupled receptor signaling pathway [IDA]
- G-protein coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger [TAS]
- cellular response to hypoxia [IDA]
- cellular response to toxic substance [IDA]
- immune response [TAS]
- negative regulation of gene expression [IDA]
- negative regulation of protein oligomerization [IDA]
- neuropeptide signaling pathway [IBA]
- opioid receptor signaling pathway [IMP]
- phospholipase C-activating G-protein coupled receptor signaling pathway [ISS]
- positive regulation of CREB transcription factor activity [IC]
- positive regulation of peptidyl-serine phosphorylation [IDA]
- protein import into nucleus, translocation [IDA]
- regulation of mitochondrial membrane potential [IDA]
- sensory perception of pain [IBA]
- synaptic transmission [IBA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
SEC61A1
Gene Ontology Biological Process
- SRP-dependent cotranslational protein targeting to membrane [IMP]
- antigen processing and presentation of exogenous peptide antigen via MHC class I [TAS]
- antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent [TAS]
- antigen processing and presentation of peptide antigen via MHC class I [TAS]
- cell growth [IMP]
- endoplasmic reticulum organization [IMP]
- posttranslational protein targeting to membrane [IMP]
- protein targeting to ER [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
Newly synthesized human delta opioid receptors retained in the endoplasmic reticulum are retrotranslocated to the cytosol, deglycosylated, ubiquitinated, and degraded by the proteasome.
We have previously shown that only a fraction of the newly synthesized human delta opioid receptors is able to leave the endoplasmic reticulum (ER) and reach the cell surface (Petaejae-Repo, U. E, Hogue, M., Laperriere, A., Walker, P., and Bouvier, M. (2000) J. Biol. Chem. 275, 13727-13736). In the present study, we investigated the fate of those receptors that are ... [more]
Throughput
- Low Throughput
Curated By
- BioGRID