+ |
UBE3A | down-regulates quantity by destabilization
polyubiquitination
|
MCM7 |
0.41 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272543 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
9852095 |
The characterization of this interaction in turn led to the discovery that Mcm7 is a substrate for both E6-AP-dependent and -independent ubiquitination and is specifically targeted for degradation by the 26 S proteasome. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CDC7 | up-regulates
phosphorylation
|
MCM7 |
0.94 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-169506 |
|
|
Homo sapiens |
|
pmid |
sentence |
21070963 |
We propose that phosphorylation of mcm4/6 s/tp sites, which are already phosphorylated in g1, allows initial mcm2-7 phosphorylation by ddk and initiation from the first origins of replication ( fig. 7ai ). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MCM7 | form complex
binding
|
MCM |
0.759 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261677 |
|
|
Homo sapiens |
|
pmid |
sentence |
19946136 |
The Mcm2-7 complex serves as the eukaryotic replicative helicase, the molecular motor that both unwinds duplex DNA and powers fork progression during DNA replication. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
EIF3E | up-regulates quantity by stabilization
binding
|
MCM7 |
0.341 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259154 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
17310990 |
Our data show that INT6 interacts with a C-terminal domain of MCM7. Collectively, our observations suggest that INT6 restrains the increased degradation of MCM7 occurring during DNA replication by protecting its polyubiquitylated derivatives from the proteasome activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |