+ |
ATM | up-regulates activity
phosphorylation
|
XRCC6 |
0.703 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274020 |
Ser27 |
QEENLEAsGDYKYSG |
Homo sapiens |
Chronic Lymphocytic Leukemia Cell |
pmid |
sentence |
26337656 |
Ku70 phosphorylation occurs within minutes of genotoxic stress and involves DNA-PKcs and/or ATM kinase activities.By using specific vectors enabling the simultaneous shRNA-mediated inhibition of endogenous Ku70 and the expression of exogenous Ku70 resistant to shRNA (i.e. S27-S33-Ku70 and A27-A33-Ku70 expressing cells), we showed that phospho-Ku70 contributes to faster but error-prone DNA repair resulting in higher levels of chromosomal breaks. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274021 |
Ser33 |
ASGDYKYsGRDSLIF |
Homo sapiens |
Chronic Lymphocytic Leukemia Cell |
pmid |
sentence |
26337656 |
Ku70 phosphorylation occurs within minutes of genotoxic stress and involves DNA-PKcs and/or ATM kinase activities.By using specific vectors enabling the simultaneous shRNA-mediated inhibition of endogenous Ku70 and the expression of exogenous Ku70 resistant to shRNA (i.e. S27-S33-Ku70 and A27-A33-Ku70 expressing cells), we showed that phospho-Ku70 contributes to faster but error-prone DNA repair resulting in higher levels of chromosomal breaks. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
PRKDC | up-regulates activity
phosphorylation
|
XRCC6 |
0.939 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274022 |
Ser27 |
QEENLEAsGDYKYSG |
Homo sapiens |
Chronic Lymphocytic Leukemia Cell |
pmid |
sentence |
26337656 |
Ku70 phosphorylation occurs within minutes of genotoxic stress and involves DNA-PKcs and/or ATM kinase activities.By using specific vectors enabling the simultaneous shRNA-mediated inhibition of endogenous Ku70 and the expression of exogenous Ku70 resistant to shRNA (i.e. S27-S33-Ku70 and A27-A33-Ku70 expressing cells), we showed that phospho-Ku70 contributes to faster but error-prone DNA repair resulting in higher levels of chromosomal breaks. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-274023 |
Ser33 |
ASGDYKYsGRDSLIF |
Homo sapiens |
Chronic Lymphocytic Leukemia Cell |
pmid |
sentence |
26337656 |
Ku70 phosphorylation occurs within minutes of genotoxic stress and involves DNA-PKcs and/or ATM kinase activities.By using specific vectors enabling the simultaneous shRNA-mediated inhibition of endogenous Ku70 and the expression of exogenous Ku70 resistant to shRNA (i.e. S27-S33-Ku70 and A27-A33-Ku70 expressing cells), we showed that phospho-Ku70 contributes to faster but error-prone DNA repair resulting in higher levels of chromosomal breaks. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
XRCC6 | up-regulates activity
relocalization
|
UBE2S |
0.353 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265079 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
27593939 |
As shown in Figure 4, we found that Ku70 (Figure 4b) and Ku80 (Figure 4c) co-immunoprecipitated with UBE2S.>Taken together, these results demonstrate that ETO enhances the UBE2S–Ku70 interaction, and UBE2S can be recruited to the same sites of DSBs with Ku70 upon ETO treatment. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC6 | form complex
binding
|
DNA-PK |
0.963 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-226023 |
|
|
Homo sapiens |
SK-BR-3 Cell |
pmid |
sentence |
17308091 |
complexes formed by interactions between Ku70, Ku80, and DNA-PKcs were well-established |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC6 | up-regulates
relocalization
|
PRKDC |
0.939 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-183276 |
|
|
Homo sapiens |
|
pmid |
sentence |
19133841 |
Ku and dna-pkcs only interact in the presence of dna and recruitment of dna-pkcs to sites of dna damage in vivo is ku-dependent. Inward translocation of ku allows dna-pkcs to interact with the extreme termini of the dna, allowing two dna-pkcs molecules to interact across the dsb in a so-called synaptic complex . This interaction stimulates the kinase activity of dna-pkcs, promoting phosphorylation in trans across the dsb (discussed in more detail below). Once assembled at the dna ends, the dna-pkcs-ku-dsb complex serves to tether the ends of the dsb together and protects the dna ends from nuclease attack. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |