+ |
ATM |
phosphorylation
|
RAD50 |
0.812 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-156077 |
Ser635 |
KLFDVCGsQDFESDL |
Homo sapiens |
|
pmid |
sentence |
17570479 |
The ms/ms fragmentation spectra (figure s7) confirmed the phosphorylation of rad50 at the predicted atm substrate site, s635, in agreement with published data |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | DNA repair in cancer |
+ |
RAD50 | up-regulates activity
binding
|
RINT1 |
0.474 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265030 |
|
|
Homo sapiens |
HFF-1 Cell |
pmid |
sentence |
16600870 |
We propose that p130, forming a complex with Rad50 through RINT-1, blocks telomerase-independent telomere lengthening in normal cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RAD50 | form complex
binding
|
MRE11/RAD50/NBS1 |
0.913 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-251506 |
|
|
|
|
pmid |
sentence |
17713585 |
The mre11_rad50_nbs1 (mrn) complex is among the earliest respondents to dna double-strand breaks (dsbs). To organize the mrn complex, the mre11 exonuclease directly binds nbs1, dna, and rad50. |
|
Publications: |
1 |
Pathways: | DNA repair in cancer |
+ |
RAD50 | up-regulates
binding
|
ATM |
0.812 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-175053 |
|
|
Homo sapiens |
|
pmid |
sentence |
21763684 |
One of the earliest events is recruitment and activation of the atm at the damaged dna sites through the mre11rad50nbs1 (mrn) sensor complex. . the mre11/rad50/nbs1 (mrn) complex maintains genomic stability by bridging dna ends and initiating dna damage signaling through activation of the atm kinase. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-181634 |
|
|
Homo sapiens |
|
pmid |
sentence |
18854157 |
One of the earliest events is recruitment and activation of the atm at the damaged dna sites through the mre11rad50nbs1 (mrn) sensor complex. . the mre11/rad50/nbs1 (mrn) complex maintains genomic stability by bridging dna ends and initiating dna damage signaling through activation of the atm kinase. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Pathways: | DNA repair in cancer |
+ |
RBL2 | up-regulates activity
binding
|
RAD50 |
0.305 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265029 |
|
|
Homo sapiens |
HFF-1 Cell |
pmid |
sentence |
16600870 |
We propose that p130, forming a complex with Rad50 through RINT-1, blocks telomerase-independent telomere lengthening in normal cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RAD50 | up-regulates
binding
|
MRE11 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-157478 |
|
|
Homo sapiens |
|
pmid |
sentence |
17713585 |
To organize the mrn complex, the mre11 exonuclease directly binds nbs1, dna, and rad50. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | DNA repair in cancer |
+ |
RAD50 | up-regulates
binding
|
BRCA1 |
0.786 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-69701 |
|
|
Homo sapiens |
Breast Cancer Cell |
pmid |
sentence |
10426999 |
Brca1 interacts in vitro and in vivo with hrad50. Brca1 is important for the cellular responses to dna damage that are mediated by the hrad50-hmre11-p95 complex. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | DNA repair in cancer |