+ |
ATR | up-regulates activity
phosphorylation
|
XRCC3 |
0.478 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262666 |
Ser225 |
PFRCEFDsQASAPRA |
Homo sapiens |
|
pmid |
sentence |
23438602 |
HXRCC3 S225 phosphorylation is mediated by ATR via an ATM-dependent signaling pathway. These data clearly indicate that ATR mediates the late activation of XRCC3 following DSB accumulation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC3 | up-regulates activity
|
CHEK2 |
0.527 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263261 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
23438602 |
Interestingly, as with ATM (40, 41), XRCC3-deficient cells exhibited RDS and impaired CHK2 activation|Notably, early activation of CHK2 in S/G2 phase was downstream of XRCC3 recruitment as well as its phosphorylation at the sites of DSBs. NBS1 also has been shown to be involved in the early activation of CHK2 in response to IR (42). It is likely that NBS1-dependent CHK2 phosphorylation is mediated through XRCC3 activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC3 | up-regulates quantity by stabilization
binding
|
RAD51 |
0.737 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-262667 |
|
|
Homo sapiens |
|
pmid |
sentence |
23438602 |
XRCC3 activation is essential for the recruitment of RAD51 to the sites of DNA lesions. It is likely that BRCA2 may directly participate in RAD51 recruitment and XRCC3 may stabilize the RAD51 filament which is in part mediated by phosphorylation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC3 | form complex
binding
|
D1-D2-G-X3 complex |
0.707 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263257 |
|
|
Homo sapiens |
|
pmid |
sentence |
18212739 |
These results argue that FANCG has a role independent of the FA core complex, and we propose that phosphorylation of serine 7 is the signalling event required for forming a discrete complex comprising FANCD1/BRCA2-FANCD2-FANCG-XRCC3 (D1-D2-G-X3). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RAD51C | up-regulates activity
relocalization
|
XRCC3 |
0.652 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263260 |
|
|
Homo sapiens |
|
pmid |
sentence |
23438602 |
It is likely that the recruitment of RAD51C to the sites of DNA lesions can promote XRCC3 phosphorylation and activate the DNA damage response pathway(s) in the S and G2 phases. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
XRCC3 | up-regulates activity
relocalization
|
RAD51 |
0.737 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-263258 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
23438602 |
We examined the effect of XRCC3 depletion on redistribution of RAD51 upon IR damage|Interestingly, cells expressing the XRCC3 S225A phosphomutant showed compromised chromatin loading of RAD51 upon IR damage (Fig. 4G) while the nuclear and cytosolic fractions of RAD51 were largely unchanged|It is likely that BRCA2 may directly participate in RAD51 recruitment and XRCC3 may stabilize the RAD51 filament which is in part mediated by phosphorylation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |