+ |
ERK1/2 | up-regulates activity
phosphorylation
|
ARRB2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274018 |
Ser14 |
TRVFKKSsPNCKLTV |
Mus musculus |
MEF Cell |
pmid |
sentence |
26324936 |
ERK1/2-dependent βarr2 phosphorylation on S14 and T276 induces CXCR4 intracellular sequestration. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274019 |
Thr276 |
FCKVYTItPLLSDNR |
Mus musculus |
MEF Cell |
pmid |
sentence |
26324936 |
ERK1/2-dependent βarr2 phosphorylation on S14 and T276 induces CXCR4 intracellular sequestration. |
|
Publications: |
2 |
Organism: |
Mus Musculus |
+ |
CSNK2A2 |
phosphorylation
|
ARRB2 |
0.314 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250977 |
Thr382 |
EFDTNYAtDDDIVFE |
in vitro |
|
pmid |
sentence |
11877451 |
We found that arrestin-3 is constitutively phosphorylated at Thr-382 and becomes dephosphorylated upon beta(2)-adrenergic receptor activation in COS-1 cells. Casein kinase II (CKII) appears to be the major kinase mediating arrestin-3 phosphorylation, since 1) Thr-382 is contained within a canonical consensus sequence for CKII phosphorylation and 2) wild type arrestin-3 but not a T382A mutant is phosphorylated by CKII in vitro. | However, additional analysis reveals that arrestin-3 phosphorylation may regulate formation of a large arrestin-3-containing protein complex. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
MAP2K1 | up-regulates activity
phosphorylation
|
ARRB2 |
0.569 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252027 |
Thr382 |
EFDTNYAtDDDIVFE |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
28169830 |
Here, we show that activation of serotonin 5-HT2C receptors, which engage Erk1/2 pathway via a _-arrestin-dependent mechanism, promotes MEK-dependent _-arrestin2 phosphorylation at Thr383 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CSNK2A1 |
phosphorylation
|
ARRB2 |
0.324 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250829 |
Thr382 |
EFDTNYAtDDDIVFE |
in vitro |
|
pmid |
sentence |
11877451 |
We found that arrestin-3 is constitutively phosphorylated at Thr-382 and becomes dephosphorylated upon beta(2)-adrenergic receptor activation in COS-1 cells. Casein kinase II (CKII) appears to be the major kinase mediating arrestin-3 phosphorylation, since 1) Thr-382 is contained within a canonical consensus sequence for CKII phosphorylation and 2) wild type arrestin-3 but not a T382A mutant is phosphorylated by CKII in vitro. | However, additional analysis reveals that arrestin-3 phosphorylation may regulate formation of a large arrestin-3-containing protein complex. |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
SMO | up-regulates
binding
|
ARRB2 |
0.647 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-199153 |
|
|
Homo sapiens |
|
pmid |
sentence |
23074268 |
Grk2-mediated phosphorylation of vertebrate smo allows smo to bind to beta-arrestins 1 or 2 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-132759 |
|
|
Homo sapiens |
|
pmid |
sentence |
15618519 |
Grk2-mediated phosphorylation of vertebrate smo allows smo to bind to beta-arrestins 1 or 2 |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
ARRB2 | up-regulates activity
binding
|
INPP5D |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261428 |
|
|
Homo sapiens |
|
pmid |
sentence |
24817116 |
We identified a new adaptor beta-arrestin 2 that associates with phosphorylated TIGIT and mediates recruitment of inositol phosphatase SHIP1 through the ITT-like motif (Fig. 7). Finally, SHIP1 impairs TRAF6 autoubiquitination to abolish NF-kappaB activation, leading to inhibition of IFN- gamma production in NK cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARRB2 | down-regulates activity
relocalization
|
SLC9A5 |
0.406 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275506 |
|
|
|
|
pmid |
sentence |
21296876 |
Internalization of the Na(+)/H(+) exchanger NHE5 into recycling endosomes is enhanced by the endocytic adaptor proteins beta-arrestin1 and -2, best known for their preferential recognition of ligand-activated G protein-coupled receptors (GPCRs) |
|
Publications: |
1 |
+ |
ARRB2 | up-regulates
binding
|
KIF3A |
0.623 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-199107 |
|
|
Homo sapiens |
|
pmid |
sentence |
23074268 |
Betaarrestin 2 was subsequentialy shown to bridge smo to the kinestesin motor kif3 to promote ciliary accumulation of smo in mammalian cells |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-148773 |
|
|
Homo sapiens |
|
pmid |
sentence |
16908539 |
We demonstrate that _-arrestins mediate the activity-dependent interaction of smo and the kinesin motor protein kif3a. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
ARRB2 | down-regulates activity
binding
|
ADRB1 |
0.481 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256502 |
|
|
in vitro |
|
pmid |
sentence |
2163110 |
The protein, termed beta-arrestin, was expressed and partially purified. It inhibited the signaling function of beta ARK-phosphorylated beta-adrenergic receptors by more than 75 percent, but not that of rhodopsin. It is proposed that beta-arrestin in concert with beta ARK effects homologous desensitization of beta-adrenergic receptors |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
ARRB2 | down-regulates activity
binding
|
ADRB2 |
0.713 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256501 |
|
|
in vitro |
|
pmid |
sentence |
2163110 |
The protein, termed beta-arrestin, was expressed and partially purified. It inhibited the signaling function of beta ARK-phosphorylated beta-adrenergic receptors by more than 75 percent, but not that of rhodopsin. It is proposed that beta-arrestin in concert with beta ARK effects homologous desensitization of beta-adrenergic receptors |
|
Publications: |
1 |
Organism: |
In Vitro |
+ |
TIGIT | up-regulates activity
binding
|
ARRB2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261482 |
|
|
Homo sapiens |
Natural Killer Cell |
pmid |
sentence |
24817116 |
With TIGIT/PVR engagement, cytoplasmic TIGIT was phosphorylated at Tyr-225 and Tyr-231 residues. Phosphorylated Tyr-225 recruits adaptor protein beta arrestin 2|TIGIT/PVR signaling mediates suppression of IFN- gamma production via the NF-kappaB pathway. We identified a new adaptor β-arrestin 2 that associates with phosphorylated TIGIT and mediates recruitment of inositol phosphatase SHIP1 through the ITT-like motif (Fig. 7). Finally, SHIP1 impairs TRAF6 autoubiquitination to abolish NF-kappaB activation, leading to inhibition of IFN- gamma production in NK cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARRB2 | up-regulates quantity by stabilization
binding
|
MDM2 |
0.444 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272592 |
|
|
Homo sapiens |
SAOS-2 Cell |
pmid |
sentence |
12488444 |
Our current results demonstrated that the binding of Mdm2 to beta-arrestin 2 was significantly enhanced by stimulation of GPCRs. Activation of GPCRs led to formation of a ternary complex of Mdm2, beta-arrestin 2, and GPCRs and thus recruited Mdm2 to GPCRs at plasma membrane. Moreover, the binding of beta-arrestin 2 to Mdm2 suppressed the self-ubiquitination of Mdm2 and consequently reduced the Mdm2-mediated p53 degradation and ubiquitination. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |