+ |
AKT2 | up-regulates quantity by stabilization
phosphorylation
|
ATP7A |
0.263 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272269 |
Ser1424 |
SYELPARsQIGQKSP |
Mus musculus |
|
pmid |
sentence |
29301787 |
Akt2 (Protein Kinase B Beta) Stabilizes ATP7A, a Copper Transporter for Extracellular Superoxide Dismutase, in Vascular Smooth Muscle: Novel Mechanism to Limit Endothelial Dysfunction in Type 2 Diabetes Mellitus|Immunoprecipitation, in vitro kinase assay, and mass spectrometry analysis reveal that insulin stimulates Akt2 binding to ATP7A to induce phosphorylation at Ser1424/1463/1466 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272268 |
Ser1463 |
IVNYSRAsINSLLSD |
Mus musculus |
|
pmid |
sentence |
29301787 |
Akt2 (Protein Kinase B Beta) Stabilizes ATP7A, a Copper Transporter for Extracellular Superoxide Dismutase, in Vascular Smooth Muscle: Novel Mechanism to Limit Endothelial Dysfunction in Type 2 Diabetes Mellitus|Immunoprecipitation, in vitro kinase assay, and mass spectrometry analysis reveal that insulin stimulates Akt2 binding to ATP7A to induce phosphorylation at Ser1424/1463/1466 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272270 |
Ser1466 |
YSRASINsLLSDKRS |
Mus musculus |
|
pmid |
sentence |
29301787 |
Akt2 (Protein Kinase B Beta) Stabilizes ATP7A, a Copper Transporter for Extracellular Superoxide Dismutase, in Vascular Smooth Muscle: Novel Mechanism to Limit Endothelial Dysfunction in Type 2 Diabetes Mellitus|Immunoprecipitation, in vitro kinase assay, and mass spectrometry analysis reveal that insulin stimulates Akt2 binding to ATP7A to induce phosphorylation at Ser1424/1463/1466 |
|
Publications: |
3 |
Organism: |
Mus Musculus |
+ |
ATP7A | up-regulates activity
|
SOD3 |
0.684 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272267 |
|
|
Mus musculus |
|
pmid |
sentence |
29301787 |
Copper transporter ATP7A (copper-transporting/ATPase) is required for full activation of SOD3 (extracellular superoxide dismutase), which is secreted from vascular smooth muscle cells (VSMCs) and anchors to endothelial cell surface to preserve endothelial function by scavenging extracellular superoxide. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
ATP7A | up-regulates quantity
relocalization
|
copper(1+) |
0.8 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272298 |
|
|
|
|
pmid |
sentence |
28389643 |
Menkes disease (MD) is caused by mutations in ATP7A, encoding a copper- transporting P-type ATPase which exhibits copper-dependent trafficking. ATP7A is found in the Trans-Golgi Network (TGN) at low copper concentrations, and in the post-Golgi compartments and the plasma membrane at higher concentrations. |
|
Publications: |
1 |