+ |
PTPRH | down-regulates
dephosphorylation
|
INSR |
0.273 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-76072 |
Tyr1185 |
FGMTRDIyETDYYRK |
Homo sapiens |
|
pmid |
sentence |
10734133 |
These results, combined with secondary dephosphorylation tests, confirm and extend earlier findings that ptp-1b and t-cell ptp are physiological enzymes for the insulin receptor kinase |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-76076 |
Tyr1189 |
RDIYETDyYRKGGKG |
Homo sapiens |
|
pmid |
sentence |
10734133 |
These results, combined with secondary dephosphorylation tests, confirm and extend earlier findings that ptp-1b and t-cell ptp are physiological enzymes for the insulin receptor kinase |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-76080 |
Tyr1190 |
DIYETDYyRKGGKGL |
Homo sapiens |
|
pmid |
sentence |
10734133 |
These results, combined with secondary dephosphorylation tests, confirm and extend earlier findings that ptp-1b and t-cell ptp are physiological enzymes for the insulin receptor kinase |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-76084 |
Tyr999 |
YASSNPEyLSASDVF |
Homo sapiens |
|
pmid |
sentence |
10734133 |
These results, combined with secondary dephosphorylation tests, confirm and extend earlier findings that ptp-1b and t-cell ptp are physiological enzymes for the insulin receptor kinase |
|
Publications: |
4 |
Organism: |
Homo Sapiens |
+ |
PTPRH | down-regulates activity
dephosphorylation
|
EGFR |
0.292 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277090 |
|
|
Homo sapiens |
|
pmid |
sentence |
28065597 |
We further found that PTPRH and PTPRB directly dephosphorylate EGFR and repress its downstream signaling. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PTPRH | down-regulates activity
dephosphorylation
|
GHR |
0.298 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-248802 |
|
|
Cricetulus griseus |
CHO Cell |
pmid |
sentence |
12907755 |
Protein tyrosine phosphatases (PTPs) play key roles in switching off tyrosine phosphorylation cascades, such as initiated by cytokine receptors. We have used substrate-trapping mutants of a large set of PTPs to identify members of the PTP family that have substrate specificity for the phosphorylated human GH receptor (GHR) intracellular domain. Among 31 PTPs tested, T cell (TC)-PTP, PTP-beta, PTP1B, stomach cancer-associated PTP 1 (SAP-1), Pyst-2, Meg-2, and PTP-H1 showed specificity for phosphorylated GHR |
|
Publications: |
1 |
Organism: |
Cricetulus Griseus |