+ |
GPER1 | up-regulates activity
binding
|
GNG2 |
0.357 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251104 |
|
|
|
|
pmid |
sentence |
10696571 |
GPCRs transduce their signal via G-protein heterotrimers (αβγ) that dissociate in free Gα-subunit protein and Gβγ-subunit protein complexes following ligand stimulation; GNG2 stands for the subunit γ, which dissociates from the receptor after the binding of GTP on α-subunit. |
|
Publications: |
1 |
+ |
17beta-estradiol | up-regulates
chemical activation
|
GPER1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-160778 |
|
|
Homo sapiens |
|
pmid |
sentence |
18262661 |
Recent studies have revealed the contribution of a novel estrogen receptor gpr30, which belongs to the family of seven-transmembrane g-protein-coupled receptors, to many of the rapid biological responses to estrogen. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-269752 |
|
|
Chlorocebus aethiops |
COS-7 Cell |
pmid |
sentence |
15705806 |
Competition binding assays of E2-Alexa 633 binding with 17β-estradiol demonstrated a Ki for 17β-estradiol of approximately 6.6 nM for GPR30 (Fig. 2F). These results demonstrate that a classic GPCR superfamily member directly binds a sex steroid hormone and that GPR30 is an estrogen-binding receptor. |Activating GPR30 by estrogen resulted in intracellular calcium mobilization and synthesis of phosphatidylinositol 3,4,5-trisphosphate in the nucleus. |
|
Publications: |
2 |
Organism: |
Homo Sapiens, Chlorocebus Aethiops |
+ |
GPER1 | up-regulates
|
1D-myo-inositol 1,4,5-trisphosphate |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-186206 |
|
|
Homo sapiens |
|
pmid |
sentence |
19549922 |
Gpr30 also stimulates the pi3k pathway, elevating cellular pip3 levels, which is also predicted to activate nr5a receptors by direct binding of pip3 to the ligand binding domain . |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
tamoxifen | up-regulates
chemical activation
|
GPER1 |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-130395 |
|
|
Homo sapiens |
|
pmid |
sentence |
15539556 |
The finding that the antiestrogens tamoxifen and ici 182,780, and an environmental estrogen, ortho,para-dichlorodiphenyldichloroethylene (o,p'-dde), have high binding affinities to the receptor and mimic the actions of e2 has important implications for both the development and treatment of estrogen-dependent breast cancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GPER1 | up-regulates
binding
|
GNAQ |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-195320 |
|
|
Homo sapiens |
Neutrophil |
pmid |
sentence |
22203955 |
However, grpr preferentially couples to galfaq proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GPER1 | up-regulates
binding
|
EGFR |
0.4 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-115988 |
|
|
Homo sapiens |
Breast Cancer Cell |
pmid |
sentence |
11897506 |
Gpcr-mediated transactivation of egfrs by estrogen provides a previously unappreciated mechanism of cross-talk between estrogen and serum growth factors, and explains prior data reporting the egf-like effects of estrogen |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
GPER1 | up-regulates activity
binding
|
GNB1 |
0.357 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251103 |
|
|
|
|
pmid |
sentence |
10696571 |
GPCRs transduce their signal via G-protein heterotrimers (αβγ) that dissociate in free Gα-subunit protein and Gβγ-subunit protein complexes following ligand stimulation; GNB1 stands for the subunit β, which dissociates from the receptor after the binding of GTP on α-subunit. |
|
Publications: |
1 |
+ |
GPER1 | up-regulates activity
binding
|
GNAS |
0.353 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251102 |
|
|
|
|
pmid |
sentence |
10696571 |
GPCRs transduce their signal via G-protein heterotrimers (αβγ) that dissociate in free Gα-subunit protein and Gβγ-subunit protein complexes following ligand stimulation; the activated receptor induces a conformational change in the associated G protein α-subunit leading to release of GDP followed by binding of GTP and α-subunit dissociation from the receptor. |
|
Publications: |
1 |