+ |
GRK2 | down-regulates activity
phosphorylation
|
OXTR |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270329 |
|
|
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
16179383 |
Recent experiments in COS-7 cells transfected with OTR have demonstrated that a rapid GRK2-mediated phosphorylation of the agonist-occupied OTR is a key first step leading to its desensitization, and that it precedes and is required for β-arrestin-dependent internalization |
|
Publications: |
1 |
Organism: |
Chlorocebus Aethiops |
Pathways: | Oxytocin signaling |
+ |
OXTR | up-regulates activity
binding
|
GNAL |
0.252 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256936 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
OXTR | up-regulates activity
binding
|
GNAQ |
0.533 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270332 |
|
|
Homo sapiens |
|
pmid |
sentence |
30739093 |
OT binds to its cognate G protein–coupled receptor (OTR) and exerts diverse effects, including stimulation (Gs) or inhibition (Gi/o) of adenylyl cyclase, stimulation of potassium channel currents (Gi), and activation of phospholipase C (Gq). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-257266 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
OXTR | up-regulates activity
binding
|
GNAS |
0.409 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270331 |
|
|
Homo sapiens |
|
pmid |
sentence |
30739093 |
OT binds to its cognate G protein–coupled receptor (OTR) and exerts diverse effects, including stimulation (Gs) or inhibition (Gi/o) of adenylyl cyclase, stimulation of potassium channel currents (Gi), and activation of phospholipase C (Gq). |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256793 |
|
|
Homo sapiens |
|
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
oxytocin | up-regulates activity
chemical activation
|
OXTR |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-257556 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
OXTR | up-regulates activity
binding
|
GNAI1 |
0.429 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-257065 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270330 |
|
|
Homo sapiens |
|
pmid |
sentence |
30739093 |
OT binds to its cognate G protein–coupled receptor (OTR) and exerts diverse effects, including stimulation (Gs) or inhibition (Gi/o) of adenylyl cyclase, stimulation of potassium channel currents (Gi), and activation of phospholipase C (Gq). |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
Oxytocin | up-regulates
binding
|
OXTR |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-16758 |
|
|
Homo sapiens |
|
pmid |
sentence |
1313946 |
The oxytocin receptor, expressed in xenopus oocytes, specifically responds to oxytocin and induces an inward membrane current |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |
+ |
OXTR | up-regulates activity
binding
|
GNA14 |
0.409 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-257332 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
OXTR | up-regulates activity
binding
|
DRD2 |
0.383 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270333 |
|
|
Rattus norvegicus |
|
pmid |
sentence |
27425032 |
Dopamine D2 receptor (D2R)–oxytocin receptor (OTR) interactions exist within heterocomplexes with facilitatory effects on D2R recognition and Gi/o coupling. Dopamine D2 receptor (D2R)–oxytocin receptor (OTR) interactions exist within heterocomplexes with facilitatory effects on D2R recognition and Gi/o coupling. |
|
Publications: |
1 |
Organism: |
Rattus Norvegicus |
Pathways: | Oxytocin signaling |
+ |
OXTR | up-regulates activity
binding
|
GNAI3 |
0.427 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-257178 |
|
|
Homo sapiens |
HEK-293A Cell |
pmid |
sentence |
31160049 |
Here we systematically quantified ligand-induced interactions between 148 GPCRs and all 11 unique G alpha subunit C-termini. For each receptor, we probed chimeric G alpha subunit activation via a transforming growth factor-alpha (TGF alpha) shedding response in HEK293 cells lacking endogenous Gq/11- and G12/13- signaling. | We defined positive coupling if any member of the subfamily scored LogRAi ≥ -1 and negative coupling if all of the members scored LogRAi < -1 (Figure 3A-B). ROC analysis gives AUC = 0.78 (Figure S4A) when considering high-confidence known coupling data and suggested a threshold of LogRAi ≥ -1.0 for defining true couplings. | The score associated to this interaction has a LogRAi ≥ -1.0. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PDPK1 | up-regulates activity
phosphorylation
|
OXTR |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268577 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
35104164 |
We found that Ser261 in OXTR was phosphorylated by protein kinase D1 (PKD1).|In HEK293A cells, the PKD1-mediated phosphorylation of OXTR promoted its binding to Gq protein and, in turn, OXTR-mediated phosphorylation of PKD1, indicating a positive feedback loop. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
Oxytocin | up-regulates activity
binding
|
OXTR |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268545 |
|
|
Homo sapiens |
|
pmid |
sentence |
11274341 |
The neurohypophysial peptide oxytocin (OT) and OT-like hormones facilitate reproduction in all vertebrates at several levels. The major site of OT gene expression is the magnocellular neurons of the hypothalamic paraventricular and supraoptic nuclei. In response to a variety of stimuli such as suckling, parturition, or certain kinds of stress, the processed OT peptide is released from the posterior pituitary into the systemic circulation.| The OT receptor is a typical class I G protein-coupled receptor that is primarily coupled via G(q) proteins to phospholipase C-beta. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Oxytocin signaling |