+ |
ATR | up-regulates activity
phosphorylation
|
RAD17 |
0.853 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-111248 |
Ser646 |
ETWSLPLsQNSASEL |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
11687627 |
Here we demonstrate that atr but not atm phosphorylates the human rad17 (hrad17) checkpoint protein on ser(635) and ser(645) in vitro.The rfc-related checkpoint protein rad17, a phosphorylation substrate of atr, is critical for atr-mediated checkpoint signaling and cell survival. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-111252 |
Ser656 |
SASELPAsQPQPFSA |
Homo sapiens |
|
pmid |
sentence |
11687627 |
Here we demonstrate that atr but not atm phosphorylates the human rad17 (hrad17) checkpoint protein on ser(635) and ser(645) in vitro.The rfc-related checkpoint protein rad17, a phosphorylation substrate of atr, is critical for atr-mediated checkpoint signaling and cell survival. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
ATM |
phosphorylation
|
RAD17 |
0.841 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-73520 |
Ser646 |
ETWSLPLsQNSASEL |
Homo sapiens |
|
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-73524 |
Ser656 |
SASELPAsQPQPFSA |
Homo sapiens |
|
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: |
Homo Sapiens |