+ |
PRKCA | up-regulates activity
phosphorylation
|
ARRB1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276619 |
Ser163 |
EKIHKRNsVRLVIRK |
Homo sapiens |
JURKAT Cell |
pmid |
sentence |
24502978 |
We demonstrate that β-arrestin-1 recruitment to the TCR, and bystander TCR and CXCR4 downregulation, are mechanistically mediated by the TCR-triggered PKC-mediated phosphorylation of β-arrestin-1 at Ser163. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAPK1 | down-regulates
phosphorylation
|
ARRB1 |
0.717 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-67630 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
10347142 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-129585 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
15456867 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-183480 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
19153083 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
MAPK3 | down-regulates
phosphorylation
|
ARRB1 |
0.705 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-67634 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
10347142 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-129589 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
15456867 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-183484 |
Ser412 |
EEEDGTGsPQLNNR |
Homo sapiens |
|
pmid |
sentence |
19153083 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
SRC | down-regulates
phosphorylation
|
ARRB1 |
0.67 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-154564 |
Tyr54 |
YLKERRVyVTLTCAF |
Homo sapiens |
|
pmid |
sentence |
17456551 |
Using fluorescently tagged proteins combined with resonance energy transfer and image cross-correlation spectroscopy approaches, we show in live cells that beta2-adaptin phosphorylation is an important regulatory process for the dissociation of beta-arrestin-AP-2 complexes in CCPs. Finally, we show that beta2-adaptin phosphorylation is involved in the early steps of receptor internalization. Our findings not only unveil beta2-adaptin as a new Src target during AT1R internalization, but also support the role of receptor-mediated signaling in the control of clathrin-dependent endocytosis of receptors. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARRB1 | up-regulates
binding
|
KIF3A |
0.532 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-178672 |
|
|
Homo sapiens |
|
pmid |
sentence |
18497258 |
Kif3a is essential for shh-mediated signaling in mammalian systems (5), and we identified kif3a as a arr1 binding partner in a proteomics screen (18). To test whether arrs, smo, and kif3a might work in concert. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ERK1/2 | down-regulates
phosphorylation
|
ARRB1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270190 |
|
|
Homo sapiens |
|
pmid |
sentence |
10347142 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ARRB1 | down-regulates activity
relocalization
|
SLC9A5 |
0.41 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275505 |
|
|
|
|
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 |
+ |
SMO | up-regulates
binding
|
ARRB1 |
0.62 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-199150 |
|
|
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-132678 |
|
|
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 |
+ |
Gbeta | down-regulates
phosphorylation
|
ARRB1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-270094 |
|
|
Homo sapiens |
|
pmid |
sentence |
10347142 |
Erk1 and erk2 phosphorylate beta-arrestin1 at ser-412 in vitro. . in the resting state, cytosolic arrestin1 proteins are constitutively phosphorylated by extracellular signal-regulated kinase (erk) at ser412, located within their distal c terminus. erk-phosphorylated arrestin1 is unable to associate with clathrin cages, whereas this constraint is removed upon its dephosphorylation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |