+ |
USP8 | up-regulates quantity by stabilization
deubiquitination
|
BACE1 |
0.462 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259101 |
Lys501 |
ADDISLLk |
Homo sapiens |
H4 Neuroglioma Cell |
pmid |
sentence |
27302062 |
Accordingly, we reported that BACE1 is ubiquitinated at lysine 501 and that lack of ubiquitination at lysine 501 produces BACE1 stabilization.Our findings demonstrate that USP8 plays a key role in the trafficking and degradation of BACE1 by deubiquitinating lysine 501. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP8 | up-regulates quantity by stabilization
deubiquitination
|
EGFR |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259103 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16120644 |
Here, we describe the role of a deubiquitinating enzyme UBPY/USP8 in the down-regulation of epidermal growth factor (EGF) receptor (EGFR). Overexpression of UBPY reduced the ubiquitination level of EGFR and delayed its degradation in EGF-stimulated cells. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259102 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
20736164 |
USP8 is known to deubiquitinate EGFR in response to ligand stimulation. USP8 depletion accelerates receptor turnover, whereas loss of hepatocyte growth factor-regulated substrate (Hrs) rescues this phenotype, indicating that USP8 protects EGFR from degradation via an Hrs-dependent pathway. [..]As EGFR stabilization against lysosomal turnover requires deubiquitination by USP8. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
USP8 | up-regulates quantity
deubiquitination
|
BACE1 |
0.462 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266905 |
|
|
Homo sapiens |
H4 Neuroglioma Cell |
pmid |
sentence |
27302062 |
Here, we report that RNAi-mediated depletion of USP8 reduced levels of both ectopically expressed and endogenous BACE1 in H4 human neuroglioma cells. Moreover, USP8 depletion increased BACE1 ubiquitination, promoted BACE1 accumulation in the early endosomes and late endosomes/lysosomes, and decreased levels of BACE1 in the recycling endosomes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP8 | up-regulates quantity by stabilization
deubiquitination
|
RNF41 |
0.875 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259105 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
23750007 |
Ubiquitin-specific protease 8 (USP8), an RNF41-interacting deubiquitylating enzyme (DUB) stabilizes RNF41 and is involved in trafficking of various transmembrane proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP8 | up-regulates quantity
binding
|
STAM |
0.551 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266904 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16520378 |
Stability of the UBPY binding partner STAM is dramatically compromised in UBPY knockdown cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
RNF41 | down-regulates quantity by destabilization
ubiquitination
|
USP8 |
0.875 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259106 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
23750007 |
RNF41 redistributes and ubiquitylates USP8, and reduces USP8 levels. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP8 | down-regulates quantity
destabilization
|
EGFR |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266902 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16520378 |
Degradation of acutely stimulated receptor tyrosine kinases, epidermal growth factor receptor and Met, is strongly inhibited in UBPY knockdown cells suggesting that UBPY function is essential for growth factor receptor down-regulation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
USP8 | down-regulates quantity
destabilization
|
MET |
0.432 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266903 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
16520378 |
Degradation of acutely stimulated receptor tyrosine kinases, epidermal growth factor receptor and Met, is strongly inhibited in UBPY knockdown cells suggesting that UBPY function is essential for growth factor receptor down-regulation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |