+ |
CDK2 | up-regulates
phosphorylation
|
FOXK2 |
0.376 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-167830 |
Ser373 |
SSRSAPAsPNHAGVL |
Homo sapiens |
|
pmid |
sentence |
20810654 |
We have mapped two cdk phosphorylation sites, serines 368 and 423, which play a role in defining foxk2 function through regulating its stability and its activity as a transcriptional repressor protein. These two cdk sites appear vital for foxk2 function because expression of a mutant lacking these sites cannot be tolerated and causes apoptosis. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-167834 |
Ser428 |
FAQSAPGsPLSSQPV |
Homo sapiens |
|
pmid |
sentence |
20810654 |
We have mapped two cdk phosphorylation sites, serines 368 and 423, which play a role in defining foxk2 function through regulating its stability and its activity as a transcriptional repressor protein. These two cdk sites appear vital for foxk2 function because expression of a mutant lacking these sites cannot be tolerated and causes apoptosis. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
CDK1 | up-regulates
phosphorylation
|
FOXK2 |
0.38 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-167822 |
Ser373 |
SSRSAPAsPNHAGVL |
Homo sapiens |
|
pmid |
sentence |
20810654 |
We have mapped two cdk phosphorylation sites, serines 368 and 423, which play a role in defining foxk2 function through regulating its stability and its activity as a transcriptional repressor protein. These two cdk sites appear vital for foxk2 function because expression of a mutant lacking these sites cannot be tolerated and causes apoptosis. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-167826 |
Ser428 |
FAQSAPGsPLSSQPV |
Homo sapiens |
|
pmid |
sentence |
20810654 |
We have mapped two cdk phosphorylation sites, serines 368 and 423, which play a role in defining foxk2 function through regulating its stability and its activity as a transcriptional repressor protein. These two cdk sites appear vital for foxk2 function because expression of a mutant lacking these sites cannot be tolerated and causes apoptosis. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
SOX8 | up-regulates quantity by expression
transcriptional regulation
|
FOXK2 |
0.293 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273613 |
|
|
Homo sapiens |
Immature Ovarian Follicle |
pmid |
sentence |
32550913 |
We showed for the first time that Aurora-A interacts directly with SOX8 and phosphorylates the protein at Ser327 to further regulate the SOX8/FOXK1 axis, which modulates cell senescence and glycolysis, ultimately leading to cisplatin resistance.. Our results showed that SOX8 targets FOXK1, thereby regulating its transcription, which has significant impacts on senescence, glycolysis and chemoresistance in ovarian cancer. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |