+ |
PLK1 | down-regulates quantity by destabilization
phosphorylation
|
TEX14 |
0.353 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273529 |
Ser437 |
QKAATVKsDIYSFSM |
Homo sapiens |
|
pmid |
sentence |
22405274 |
We show that phosphorylation of Tex14 by Plk1 during metaphase is required for proteosome dependent degradation of Tex14 and transition from metaphase to anaphase. Phosphorylation of Tex14 Ser431 by Plk1 promotes Tex14 depletion. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-279646 |
|
|
Homo sapiens |
|
pmid |
sentence |
22405274 |
In addition, we demonstrate that phosphorylation of Tex14 by Plk1 during metaphase promotes APC Cdc20 -mediated Tex14 degradation. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
Tissue: |
Testis |
+ |
CDK1 | down-regulates quantity by destabilization
phosphorylation
|
TEX14 |
0.333 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273523 |
Thr618 |
EEASSPStGQPSLCS |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
22405274 |
Cdk1 phosphorylation of Tex14 is required for the Tex14-Plk1 interaction |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273524 |
Thr727 |
SNLNNMStTEEYLIS |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
22405274 |
Cdk1 phosphorylation of Tex14 is required for the Tex14-Plk1 interaction |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273522 |
Thr728 |
NLNNMSTtEEYLISK |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
22405274 |
Cdk1 phosphorylation of Tex14 is required for the Tex14-Plk1 interaction |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
CDK1 | up-regulates activity
phosphorylation
|
TEX14 |
0.333 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-279677 |
|
|
Homo sapiens |
|
pmid |
sentence |
22405274 |
Cdk1 phosphorylation of Tex14 is required for the Tex14-Plk1 interaction.|While, mutation of individual PBDs in Tex14 partially reduces Cdk1 dependent phosphorylation levels and inhibits the ability of Tex14 to interact with Plk1 and to localize to KTs, mutation of all identified PBDs has a much more significant impact on binding. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |