+ |
AKT | up-regulates activity
phosphorylation
|
SH2B2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-248042 |
Ser598 |
SARSRSNsAERLLEA |
Mus musculus |
|
pmid |
sentence |
16141217 |
This study identifies APS as a novel physiological substrate for PKB and the first serine phosphorylation site on APS |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
AKT1 |
phosphorylation
|
SH2B2 |
0.409 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252577 |
Ser598 |
SARSRSNsAERLLEA |
Mus musculus |
|
pmid |
sentence |
16141217 |
Serine 588 of APS is a newly identified target for protein kinase B in intact cells and in vitro. The precise function of this PKB-mediated phosphorylation event is not entirely clear but may be responsible for regulating cellular localization and will be the subject of future investigation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
AKT1 | up-regulates activity
phosphorylation
|
SH2B2 |
0.409 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252557 |
Ser598 |
SARSRSNsAERLLEA |
Mus musculus |
|
pmid |
sentence |
16141217 |
This study identifies APS as a novel physiological substrate for PKB and the first serine phosphorylation site on APS |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
AKT |
phosphorylation
|
SH2B2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251487 |
Ser598 |
SARSRSNsAERLLEA |
Mus musculus |
|
pmid |
sentence |
16141217 |
Serine 588 of APS is a newly identified target for protein kinase B in intact cells and in vitro. The precise function of this PKB-mediated phosphorylation event is not entirely clear but may be responsible for regulating cellular localization and will be the subject of future investigation. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
NTRK1 | up-regulates
phosphorylation
|
SH2B2 |
0.531 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-62619 |
|
|
Homo sapiens |
Neuron |
pmid |
sentence |
9856458 |
Two substrates of trk kinases, raps and sh2-b. raps and sh2-b mediate trk signaling in developing neurons |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SH2B2 | up-regulates
binding
|
CBL |
0.631 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109691 |
|
|
Homo sapiens |
|
pmid |
sentence |
11498022 |
Aps couples c-cbl to theinsulinreceptor, resulting in ubiquitination of theinsulinreceptor. The aps adapter protein couples theinsulinreceptor to the phosphorylation of c-cbl and facilitates ligand-stimulated ubiquitination of theinsulinreceptor. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-78337 |
|
|
Cricetulus griseus |
Ovary Cell Line |
pmid |
sentence |
10854852 |
APS-mediated recruitment of c-Cbl to the insulin receptor led to rapid ubiquitination of the insulin receptor beta-subunit in CHO. T-APS but not in parental CHO.T cells. These results suggest that the function of APS is to facilitate coupling of the insulin receptor to c-Cbl in order to catalyse the ubiquitination of the receptor and initiation of internalisation or degradation. |
|
Publications: |
2 |
Organism: |
Homo Sapiens, Cricetulus Griseus |
Tissue: |
Ovary |
+ |
SH2B2 | down-regulates
binding
|
INSR |
0.604 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109694 |
|
|
Homo sapiens |
|
pmid |
sentence |
11498022 |
APS couples c-Cbl to the insulin receptor, resulting in ubiquitination of the insulin receptor. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Tissue: |
Ovary |
+ |
PTEN | up-regulates quantity by expression
transcriptional regulation
|
SH2B2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260051 |
|
|
Homo sapiens |
|
pmid |
sentence |
11494141 |
Defects in PTEN, a tumor suppressor, have been found in cancers arising in a variety of human tissues. To elucidate the tumor-suppressive function of this gene, we have been analysing expression profiles of cancer cells after introduction of exogenous PTEN. Those experiments identified 99 candidate genes that were transcriptionally transactivated. Among them, we report here the further analyses of eight genes, EGR2/Krox-20, BPOZ, APS, HCLS1/HS1, DUSP1/MKP1, NDRG1/Drg1/RTP, NFIL3/E4BP4, and a novel gene (PINK1, PTEN-induced putative kinase). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |