+ |
CCNC | down-regulates
phosphorylation
|
NOTCH1 |
0.458 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-130592 |
|
|
Homo sapiens |
|
pmid |
sentence |
15546612 |
Purified recombinant cycc:cdk8 phosphorylates the notch icd within the tad and pest domains, and expression of cycc:cdk8 strongly enhances notch icd hyperphosphorylation and pest-dependent degradation by the fbw7/sel10 ubiquitin ligase in vivo. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCNC | down-regulates
phosphorylation
|
NOTCH |
0.458 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254309 |
|
|
Homo sapiens |
|
pmid |
sentence |
15546612 |
Purified recombinant cycc:cdk8 phosphorylates the notch icd within the tad and pest domains, and expression of cycc:cdk8 strongly enhances notch icd hyperphosphorylation and pest-dependent degradation by the fbw7/sel10 ubiquitin ligase in vivo. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCNC | up-regulates quantity by expression
transcriptional regulation
|
HES1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-130589 |
|
|
Homo sapiens |
|
pmid |
sentence |
15546612 |
Cycc:cdk8 and cyct1:cdk9/p-tefb are recruited with notch and associated coactivators (mam, skip) to the hes1 promoter in signaling cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCNC | form complex
binding
|
CKM complex |
0.919 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266685 |
|
|
Homo sapiens |
|
pmid |
sentence |
23563140 |
The CDK8 kinase module (CKM) is a conserved, dissociable Mediator subcomplex whose component subunits were genetically linked to the RNA polymerase II (RNAPII) C-terminal domain (CTD) and individually recognized as transcriptional repressors before Mediator was identified as a pre-eminent complex in eukaryotic transcription regulation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCNC | form complex
binding
|
CyclinC/CDK3 |
0.681 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273156 |
|
|
Homo sapiens |
MOLT-16 Cell |
pmid |
sentence |
25344755 |
Cyclin C was cloned as a growth-promoting G1 cyclin, and was also shown to regulate gene transcription. Here we report that in vivo cyclin C acts as a haploinsufficient tumor suppressor, by controlling Notch1 oncogene levels. Cyclin C activates an “orphan” CDK19 kinase, as well as CDK8 and CDK3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MAML1 | up-regulates
relocalization
|
CCNC |
0.423 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-130709 |
|
|
Homo sapiens |
|
pmid |
sentence |
15546612 |
Cycc:cdk8 and cyct1:cdk9/p-tefb are recruited with notch and associated coactivators (mam, skip) to the hes1 promoter in signaling cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CCNC | form complex
binding
|
CyclinC/CDK19 |
0.911 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273154 |
|
|
Homo sapiens |
MOLT-16 Cell |
pmid |
sentence |
25344755 |
We found that in MOLT-16 cells cyclin C physically interacts with CDK19 (Fig. 5a) and activates its kinase activity (Fig. 5e and Supplementary Fig. 4f,g). |
|
Publications: |
1 |
Organism: |
Homo Sapiens |