+ |
CSNK1E | up-regulates activity
phosphorylation
|
TRAF3 |
0.311 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277212 |
Ser349 |
QNWEEADsMKSSVES |
Homo sapiens |
|
pmid |
sentence |
26928339 |
CK1ɛ interacted with and phosphorylated TRAF3 at Ser349, which thereby promoted the Lys63 (K63)-linked ubiquitination of TRAF3 and subsequent recruitment of the kinase TBK1 to TRAF3. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277525 |
Tyr116 |
EILALQIyCRNESRG |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
32779804 |
We found that the interaction of CK1ε with TRAF3Y116F, TRAF3Y446F were markedly decreased compared with interactions with WT TRAF3 by Co‐IP (Figure 6C); as expected, TRAF3Y116F and TRAF3Y446F mutants exhibited reduced K63‐linked ubiquitination (Figure 6D). These data suggest that the phosphorylation of TRAF3 at Tyr 116 and Tyr 446 regulate CK1ε‐induced K63‐linked ubiquitination. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277524 |
Tyr446 |
SLYSQPFyTGYFGYK |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
32779804 |
We found that the interaction of CK1ε with TRAF3Y116F, TRAF3Y446F were markedly decreased compared with interactions with WT TRAF3 by Co‐IP (Figure 6C); as expected, TRAF3Y116F and TRAF3Y446F mutants exhibited reduced K63‐linked ubiquitination (Figure 6D). These data suggest that the phosphorylation of TRAF3 at Tyr 116 and Tyr 446 regulate CK1ε‐induced K63‐linked ubiquitination. |
|
Publications: |
3 |
Organism: |
Homo Sapiens |
+ |
PTPN6 | down-regulates activity
dephosphorylation
|
TRAF3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277527 |
Tyr116 |
EILALQIyCRNESRG |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
32779804 |
We identified a direct interaction between SHP‐1 and TRAF3; the association between these two proteins resulted in diminished recruitment of CK1ε to TRAF3 and inhibited its K63‐linked ubiquitination; SHP‐1 inhibited K63‐linked ubiquitination of TRAF3 by promoting dephosphorylation at Tyr116 and Tyr446. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277526 |
Tyr446 |
SLYSQPFyTGYFGYK |
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
32779804 |
We identified a direct interaction between SHP‐1 and TRAF3; the association between these two proteins resulted in diminished recruitment of CK1ε to TRAF3 and inhibited its K63‐linked ubiquitination; SHP‐1 inhibited K63‐linked ubiquitination of TRAF3 by promoting dephosphorylation at Tyr116 and Tyr446. |
|
Publications: |
2 |
Organism: |
Homo Sapiens |
+ |
CD40 | up-regulates activity
binding
|
TRAF3 |
0.916 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-250560 |
|
|
Homo sapiens |
|
pmid |
sentence |
18635759 |
Cd40, a tumor necrosis factor receptor (tnfr) family member, forms a complex containing adaptor molecules traf2 and traf3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | NF-KB Non Canonical |
+ |
Papain-like proteinase | down-regulates activity
deubiquitination
|
TRAF3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260246 |
|
|
Homo sapiens |
|
pmid |
sentence |
31226023 |
Overexpressing PLPro of SARS-CoV or MERS-CoV significantly reduced the expression of IFN-β and proinflammatory cytokines in MDA5-stimulated 293T cells (83).Also, SARS-CoVPLPro catalyzed deubiquitination of TNF-receptor-associated factor3 (TRAF3) and TRAF6, thereby suppressing IFN-I and proinflammatory cytokines induced by TLR7 agonist (63). The deubiquitinating activity of SARS-CoV PLPro also suppressed a constitutively active phosphomimetic IRF3, suggesting its involvement in the postactivation signaling of IRF3 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV INFLAMMATORY RESPONSE |
+ |
TRAF3 | up-regulates activity
binding
|
TBK1 |
0.9 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260156 |
|
|
Homo sapiens |
|
pmid |
sentence |
24622840 |
MAVS also interacts with STING that locates at the ER (endoplasmic reticulum), and induces the ubiquitination and dimerization of STING. The activated STING recruits TBK1 and IRF3 and contributes to the phosphorylation of IRF3 mediated by TBK1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, Innate Immune Response, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE |
+ |
TNIP1 | down-regulates activity
binding
|
TRAF3 |
0.443 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275736 |
|
|
|
|
pmid |
sentence |
21885437 |
ABIN1 interacted with the A20 regulatory molecule TAX1BP1 and was essential for the recruitment of TAX1BP1 and A20 to the noncanonical IkappaB kinases TBK1 and IKKi in response to poly(I:C) transfection. ABIN1 and TAX1BP1 together disrupted the interactions between the E3 ubiquitin ligase TRAF3 and TBK1/IKKi to attenuate lysine 63-linked polyubiquitination of TBK1/IKKi. |
|
Publications: |
1 |
+ |
TRAF3 | down-regulates quantity by destabilization
binding
|
MAP3K14 |
0.654 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-124236 |
|
|
Mus musculus |
|
pmid |
sentence |
15084608 |
Traf3 is physically associated with nik via a specific sequence motif located in the n-terminal region of nik; this molecular interaction appears to target nik for degradation by the proteasome. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | Innate Immune Response, NF-KB Non Canonical |
+ |
9b | down-regulates quantity by destabilization
|
TRAF3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260242 |
|
|
Homo sapiens |
|
pmid |
sentence |
25135833 |
SARS-coronavirus Open Reading frame-9b Suppresses Innate Immunity by Targeting Mitochondria and the MAVS/TRAF3/TRAF6 Signalosome. Acting on mitochondria, ORF-9b targets the mitochondrial-associated adaptor molecule MAVS signalosome by usurping PCBP2 and the HECT domain E3 ligase AIP4 to trigger the degradation of MAVS, TRAF3, and TRAF 6. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, SARS-CoV INFLAMMATORY RESPONSE |
+ |
TNFRSF13C | down-regulates quantity by destabilization
binding
|
TRAF3 |
0.749 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-168199 |
|
|
Homo sapiens |
B-lymphocyte, Lymphoma Cell |
pmid |
sentence |
20889926 |
Activation of br3 induces recruitment and degradation of traf3. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | NF-KB Non Canonical |
+ |
TAX1BP1 | down-regulates activity
binding
|
TRAF3 |
0.479 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-275737 |
|
|
|
|
pmid |
sentence |
21885437 |
ABIN1 interacted with the A20 regulatory molecule TAX1BP1 and was essential for the recruitment of TAX1BP1 and A20 to the noncanonical IkappaB kinases TBK1 and IKKi in response to poly(I:C) transfection. ABIN1 and TAX1BP1 together disrupted the interactions between the E3 ubiquitin ligase TRAF3 and TBK1/IKKi to attenuate lysine 63-linked polyubiquitination of TBK1/IKKi. |
|
Publications: |
1 |
+ |
TRAF3 | up-regulates quantity by expression
transcriptional regulation
|
IL10 |
0.337 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256077 |
|
|
Mus musculus |
|
pmid |
sentence |
16306937 |
TRAF3 is essential for the induction of type I interferons (IFN) and the anti-inflammatory cytokine interleukin-10 (IL-10), but is dispensable for expression of pro-inflammatory cytokines. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
OTUD5 | down-regulates activity
deubiquitination
|
TRAF3 |
0.767 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-265873 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
17991829 |
TRAF3 is an E3 ubiquitin ligase that preferentially assembled lysine-63-linked polyubiquitin chains. DUBA selectively cleaved the lysine-63-linked polyubiquitin chains on TRAF3, resulting in its dissociation from the downstream signaling complex containing TANK-binding kinase 1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
MYD88 | up-regulates activity
binding
|
TRAF3 |
0.717 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256079 |
|
|
Mus musculus |
Myeloid Cell Line |
pmid |
sentence |
16306937 |
Using MyD88 as a prototypical adaptor, we identified TNF receptor-associated factor 3 (TRAF3) as a new component of TIR signalling complexes that is recruited along with TRAF6. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | COVID-19 Causal Network, Innate Immune Response, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE |
+ |
Ub:E2 | up-regulates activity
ubiquitination
|
TRAF3 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271071 |
|
|
Homo sapiens |
|
pmid |
sentence |
34199813 |
The ubiquitination process is mediated sequentially by three classes of enzymes consisting of a Ub-activating enzyme E1, a Ub-conjugating enzyme E2, and a Ub ligase E3. Ub is first activated by E1 in an adenosine 5′-triphosphate (ATP)-dependent manner t |
|
Publications: |
1 |
Organism: |
Homo Sapiens |