+ |
MAP3K5 | up-regulates
phosphorylation
|
DAXX |
0.835 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-188321 |
Ser176 |
TNAENTAsQSPRTRG |
Homo sapiens |
|
pmid |
sentence |
19789335 |
Our data demonstrated that ask1 controls the cytoplasmic localization of daxx (fig.1). our results indicate that daxx not only activates ask1 but also is a downstream target of ask1 and that accumulated daxx further activates ask1. Thus, the daxx-ask1 positive feedback loop amplifying jnk/p38 signaling plays an important role in the cell-killing effects of stressors, such as tnfalpha. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-188325 |
Ser184 |
QSPRTRGsRRQIQRL |
Homo sapiens |
|
pmid |
sentence |
19789335 |
Our data demonstrated that ask1 controls the cytoplasmic localization of daxx (fig.1). our results indicate that daxx not only activates ask1 but also is a downstream target of ask1 and that accumulated daxx further activates ask1. Thus, the daxx-ask1 positive feedback loop amplifying jnk/p38 signaling plays an important role in the cell-killing effects of stressors, such as tnfalpha. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
MAP3K5 | up-regulates quantity by stabilization
phosphorylation
|
DAXX |
0.835 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109680 |
Ser176 |
TNAENTAsQSPRTRG |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
19789335 |
we show that TNFalpha treatment induces the accumulation of Daxx protein through ASK1 activation by preventing its proteasome-dependent degradation. ASK1 directly phosphorylates Daxx at Ser(176) and Ser(184) and Daxx is required for the sustained activation of JNK. Our results indicate that Daxx not only activates ASK1 but also is a downstream target of ASK1 and that accumulated Daxx further activates ASK1. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109684 |
Ser184 |
QSPRTRGsRRQIQRL |
Homo sapiens |
HeLa Cell |
pmid |
sentence |
19789335 |
we show that TNFalpha treatment induces the accumulation of Daxx protein through ASK1 activation by preventing its proteasome-dependent degradation. ASK1 directly phosphorylates Daxx at Ser(176) and Ser(184) and Daxx is required for the sustained activation of JNK. Our results indicate that Daxx not only activates ASK1 but also is a downstream target of ASK1 and that accumulated Daxx further activates ASK1. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
ATM | down-regulates
phosphorylation
|
DAXX |
0.514 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-200889 |
Ser564 |
LEEESPVsQLFELEI |
Homo sapiens |
|
pmid |
sentence |
23405218 |
The main phosphorylation site of daxx is identified to be ser564, which is a direct target of atm. Phosphorylation of endogenous daxx at ser564 occurs rapidly during the dna damage response and precedes p53 activation. Blockage of this phosphorylation event prevents the separation of daxx from mdm2, stabilizes mdm2, and inhibits dna damage-induced p53 activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIPK1 | down-regulates activity
phosphorylation
|
DAXX |
0.631 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260842 |
Ser668 |
KKICTLPsPPSPLAS |
Homo sapiens |
|
pmid |
sentence |
12529400 |
HIPK1 phosphorylates Daxx on Ser 669, and phosphorylation of this site is important in modulating the ability of Daxx to function as a transcriptional repressor. | Therefore, phosphorylation at Ser 669 by HIPK1 diminishes the ability of Daxx to repress transcription. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CSNK2A1 | up-regulates
phosphorylation
|
DAXX |
0.332 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-173105 |
Ser737 |
PEEIIVLsDSD |
Homo sapiens |
|
pmid |
sentence |
21474068 |
Daxx-sim is phosphorylated by ck2 kinase at residues s737 and s739. Phosphorylation promotes daxx-sim binding affinity toward sumo-1 over sumo-2/3, causing daxx preference for sumo-1 conjugation and interaction with sumo-1-modified factors. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-173109 |
Ser739 |
EIIVLSDsD |
Homo sapiens |
|
pmid |
sentence |
21474068 |
Daxx-sim is phosphorylated by ck2 kinase at residues s737 and s739. Phosphorylation promotes daxx-sim binding affinity toward sumo-1 over sumo-2/3, causing daxx preference for sumo-1 conjugation and interaction with sumo-1-modified factors. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
DAXX | down-regulates activity
binding
|
AIRE |
0.34 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-239287 |
|
|
Homo sapiens |
HeLa Cell |
pmid |
sentence |
20185822 |
The interaction between AIRE and DAXX has been validated by in vivo coimmunoprecipitation analysis and colocalization study in mammalian cells. The interaction has been further confirmed by showing in transactivation assays that DAXX exerts a strong repressive role on the transcriptional activity of AIRE. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAXX | up-regulates
binding
|
MAP3K5 |
0.835 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-60164 |
|
|
Homo sapiens |
|
pmid |
sentence |
9743501 |
Daxx was found to activate the jnk kinase kinase ask1, and overexpression of a kinase-deficient ask1 mutant inhibited fas- and daxx-induced apoptosis and jnk activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAXX | down-regulates
binding
|
FAS |
0.69 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-49473 |
|
|
Homo sapiens |
|
pmid |
sentence |
9215629 |
A c-terminal portion of daxx interacts with the fas death domain. The fas-binding domain of daxx is a dominant-negative inhibitor of both fas-induced apoptosis and jnk activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAXX | up-regulates
binding
|
MDM2 |
0.66 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-200892 |
|
|
Homo sapiens |
|
pmid |
sentence |
23405218 |
The optimal function of mdm2 requires daxx, which stabilizes mdm2 through the deubiquitinase hausp/usp7 and also directly promotes mdm2's ubiquitin ligase activity towards p53. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAXX | up-regulates
binding
|
TGFBR2 |
0.508 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-109542 |
|
|
Homo sapiens |
B-lymphocyte, Lymphoma Cell |
pmid |
sentence |
11483955 |
Tgf-beta-induced apoptosis is mediated by the adapter protein daxx that facilitates jnk activation |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
DAXX | down-regulates
|
Immortality |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256596 |
|
|
Homo sapiens |
Pancreatic Cancer Cell |
pmid |
sentence |
26428317 |
Telomere length must be maintained for the immortalization of malignant cells […] alternative lengthening of telomeres status was perfectly correlated with the loss of expression of either α-thalassemia/mental retardation syndrome X-linked (ATRX) or death domain-associated (DAXX) protein in pancreatic neuroendocrine tumors |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPOP | down-regulates quantity
ubiquitination
|
DAXX |
0.497 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-268858 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
16524876 |
These results suggest that SPOP/Cul3-ubiquitin ligase plays an essential role in the control of Daxx level and, thus, in the regulation of Daxx-mediated cellular processes, including transcriptional regulation and apoptosis. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
FAS | up-regulates
|
DAXX |
0.69 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-60167 |
|
|
Homo sapiens |
|
pmid |
sentence |
9743501 |
Fas activation induced daxx to interact with ask1 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |