+ |
AKT1 | up-regulates quantity by stabilization
phosphorylation
|
USP4 |
0.478 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-273482 |
Ser445 |
NHRLRNDsVIVDTFH |
Homo sapiens |
|
pmid |
sentence |
22706160 |
AKT-mediated phosphorylation relocates nuclear USP4 to the cytoplasm and membrane and is required for maintaining its protein stability. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP4 | down-regulates activity
deubiquitination
|
PRPF3 |
0.501 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271975 |
|
|
Homo sapiens |
|
pmid |
sentence |
20595234 |
Prp3 is deubiquitinated by Usp4 and its substrate targeting factor, the U4/U6 recycling protein Sart3, which likely facilitates ejection of U4 proteins from the spliceosome during maturation of its active site. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP4 | up-regulates quantity by stabilization
deubiquitination
|
BRAP |
0.271 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272031 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
23105109 |
Here we report on a novel interaction between the E3 ligase BRAP (also referred to as IMP), a negative regulator of the MAPK scaffold protein KSR, and two closely related deubiquitylases, USP15 and USP4. USP15 as well as USP4 oppose the autoubiquitylation of BRAP, whereas BRAP promotes the ubiquitylation of USP15. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DNPEP | down-regulates quantity by destabilization
cleavage
|
USP4 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275652 |
|
|
|
|
pmid |
sentence |
31219614 |
A further analysis showed that the hydrolysis pathway contributes to DNPEP-mediated degradation of USP4 (Supporting Information Figs. S3A–S3F). The interaction between USP4 and DNPEP was confirmed by coIP assays |
|
Publications: |
1 |