+ |
ATM |
phosphorylation
|
WRN |
0.82 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250577 |
Ser1141 |
PEKAYSSsQPVISAQ |
in vitro |
|
pmid |
sentence |
10608806 |
We determined a general phosphorylation consensus sequence for ATM and identified putative in vitro targets by using glutathione S-transferase peptides as substrates. Putative ATM in vitro targets include p95/nibrin, Mre11, Brca1, Rad17, PTS, WRN, and ATM (S440) itself. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250578 |
Ser1292 |
MTIGMHLsQAVKAGC |
in vitro |
|
pmid |
sentence |
10608806 |
We determined a general phosphorylation consensus sequence for ATM and identified putative in vitro targets by using glutathione S-transferase peptides as substrates. Putative ATM in vitro targets include p95/nibrin, Mre11, Brca1, Rad17, PTS, WRN, and ATM (S440) itself. |
|
Publications: |
2 |
Organism: |
In Vitro |
+ |
ATR | down-regulates quantity by destabilization
phosphorylation
|
WRN |
0.786 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277187 |
Ser1141 |
PEKAYSSsQPVISAQ |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
26695548 |
A serine residue, S1141, in WRN is phosphorylated in vivo by the ATR kinase in response to replication stress. ATR-mediated WRN S1141 phosphorylation leads to ubiquitination of WRN, facilitating the reversible interaction of WRN with perturbed replication forks and subsequent degradation of WRN. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
PRKDC | up-regulates
phosphorylation
|
WRN |
0.661 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-203737 |
Ser440 |
DTSYVIEsDEDLEME |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
24429382 |
Here, we identify ser-440 and -467 in wrn as major phosphorylation sites mediated by dna-pk our findings indicate that phosphorylation of ser-440 and -467 in wrn are important for relocalization of wrn to nucleoli, and that it is required for efficient dsb repair. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-203741 |
Ser467 |
DTSYVIEsDEDLEME |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
24429382 |
Here, we identify ser-440 and -467 in wrn as major phosphorylation sites mediated by dna-pk our findings indicate that phosphorylation of ser-440 and -467 in wrn are important for relocalization of wrn to nucleoli, and that it is required for efficient dsb repair. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
WRN | up-regulates activity
|
DNA_repair |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-258983 |
|
|
Homo sapiens |
|
pmid |
sentence |
19652551 |
Our work provides the first demonstration of the major importance of WRN in repair of a specific class of DSB in human cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
ABL1 | up-regulates
phosphorylation
|
WRN |
0.42 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-86497 |
|
|
Homo sapiens |
HeLa Cell, Leukemia Cell |
pmid |
sentence |
12944467 |
We thus hypothesized that wrn may interact with the abl tyrosine kinase in the dna damage response. Here, we provide evidence for a functional and physical interaction between wrn and c-abl, including wrn relocalization in response to dna damage, suggesting that this protein-protein interaction participates in a shared pathway of genome surveillance. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |