+ |
CSNK2A1 | up-regulates activity
phosphorylation
|
ATXN3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276225 |
Ser236 |
LQRALALsRQEIDME |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
19542537 |
Here we show that protein casein kinase 2 (CK2)-dependent phosphorylation controls the nuclear localization, aggregation and stability of ataxin-3 (ATXN3), the disease protein in spinocerebellar ataxia type 3 (SCA3). The main phosphorylation of ATXN3 in vivo thus occurred at serine residues within the three conserved UIMs. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276226 |
Ser335 |
SDLGDAMsEEDMLQA |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
19542537 |
Here we show that protein casein kinase 2 (CK2)-dependent phosphorylation controls the nuclear localization, aggregation and stability of ataxin-3 (ATXN3), the disease protein in spinocerebellar ataxia type 3 (SCA3). The main phosphorylation of ATXN3 in vivo thus occurred at serine residues within the three conserved UIMs. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-276224 |
Ser347 |
LQAAVTMsLETVRND |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
19542537 |
Here we show that protein casein kinase 2 (CK2)-dependent phosphorylation controls the nuclear localization, aggregation and stability of ataxin-3 (ATXN3), the disease protein in spinocerebellar ataxia type 3 (SCA3). The main phosphorylation of ATXN3 in vivo thus occurred at serine residues within the three conserved UIMs. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
GSK3B | up-regulates quantity by stabilization
phosphorylation
|
ATXN3 |
0.475 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-264821 |
Ser256 |
LRRAIQLsMQGSSRN |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
17434145 |
Phosphorylation of ataxin-3 by glycogen synthase kinase 3beta at serine 256 regulates the aggregation of ataxin-3| |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
STUB1 | down-regulates quantity by destabilization
ubiquitination
|
ATXN3 |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-278667 |
|
|
Homo sapiens |
|
pmid |
sentence |
21625540 |
Although our data show that CHIP may associate with Atx3 to ubiquitinate Atx3 in vitro, we still wonder whether CHIP is directly involved in the degradation of Atx3.|As a result, silencing of CHIP significantly increases the amount of Atx3 (XREF_FIG), suggesting that CHIP may down-regulate the Atx3 level. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
UBE4B | down-regulates quantity by destabilization
polyubiquitination
|
ATXN3 |
0.592 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271502 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
14749733 |
Mammalian E4B (UFD2a), a ubiquitin chain assembly factor (E4), copurified with the polyubiquitylation activity for ataxin-3. E4B interacted with, and thereby mediated polyubiquitylation of, ataxin-3. Collectively, these data suggest that E4B promotes the degradation of ataxin-3, and that this effect surmounts the stabilization of ataxin-3 conferred by expansion of the polyglutamine tract. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |