+ |
TLR4 | up-regulates activity
binding
|
TICAM1 |
0.844 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252067 |
|
|
Mus musculus |
|
pmid |
sentence |
22664090 |
To initiate the innate immune response, Toll-like receptors (TLRs) associate with cytoplasmic adaptor proteins through TIR (Toll/interleukin-1 receptor) domain interactions. The four principal signaling adaptor proteins include MyD88, MAL, TRIF and TRAM, and the fifth protein SARM, involved in negative regulation of TLR pathways, is usually considered a part of the TIR domain-containing adaptor protein group |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | Macrophage polarization |
+ |
DDX21 | up-regulates activity
binding
|
TICAM1 |
0.27 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260192 |
|
|
Mus musculus |
|
pmid |
sentence |
21703541 |
We demonstrated here that DDX1-DDX21-DHX36 represents a dsRNA sensor that uses the adaptor molecule TRIF to activate the NF-κB pathway and type I IFN responses in dendritic cells. Our study suggests that the DDX1-DDX21-DHX36 complex represents this missing poly I:C sensor, which uses DDX1 to bind poly I:C and uses DDX21 and DXH36 to bind TRIF. Poly I:C is a synthetic form of RNA that mimics double-stranded viral RNA. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | COVID-19 Causal Network, Innate Immune Response, SARS-CoV INNATE RESPONSE TO dsRNA |
+ |
TICAM1 | up-regulates activity
binding
|
RIPK1 |
0.723 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-216313 |
|
|
Homo sapiens |
|
pmid |
sentence |
20404851 |
TRIF also recruits the adaptor RIP1 through the distinct RIP homotypic interaction motif. RIP1 undergoes K63-linked polyubiquitination after stimulation by TLR3 agonists, and this modification is required for NF-_B activation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, Innate Immune Response, Inflammosome Activation, Macrophage polarization, SARS-CoV INFLAMMATORY RESPONSE, SARS-CoV INNATE RESPONSE TO dsRNA |
+ |
TLR2 | up-regulates activity
binding
|
TICAM1 |
0.628 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266746 |
|
|
Mus musculus |
|
pmid |
sentence |
22664090 |
To initiate the innate immune response, Toll-like receptors (TLRs) associate with cytoplasmic adaptor proteins through TIR (Toll/interleukin-1 receptor) domain interactions. The four principal signaling adaptor proteins include MyD88, MAL, TRIF and TRAM, and the fifth protein SARM, involved in negative regulation of TLR pathways, is usually considered a part of the TIR domain-containing adaptor protein group |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | EBV infection |
+ |
TRAF2 | up-regulates
polyubiquitination
|
TICAM1 |
0.442 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271427 |
|
|
Homo sapiens |
|
pmid |
sentence |
20047764 |
Here, we show that the TRAF family proteins directly bind TICAM-1 and demonstrate that TRAF2 and TRAF6 bind different sites of the N-terminal TICAM-1 and accelerate its polyubiquitination. we speculate that polyubiquitination of TICAM-1 by TRAF2 and TRAF6 is required for TICAM-1 to induce IRF-3 and NF-κB activation. This is supported by the observation that polyubiquitination of TICAM-1 was required for TRAF3-binding to TICAM-1 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
TLR9 | up-regulates activity
binding
|
TICAM1 |
0.451 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266749 |
|
|
Mus musculus |
|
pmid |
sentence |
22664090 |
To initiate the innate immune response, Toll-like receptors (TLRs) associate with cytoplasmic adaptor proteins through TIR (Toll/interleukin-1 receptor) domain interactions. The four principal signaling adaptor proteins include MyD88, MAL, TRIF and TRAM, and the fifth protein SARM, involved in negative regulation of TLR pathways, is usually considered a part of the TIR domain-containing adaptor protein group |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | EBV infection |
+ |
RNF216 | down-regulates quantity by destabilization
ubiquitination
|
TICAM1 |
0.362 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271609 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
16968706 |
Triad3A promotes proteolytic degradation of adapter proteins. A, Triad3A promotes down-regulation of TIRAP, TRIF, and RIP1 proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SARM1 | down-regulates
binding
|
TICAM1 |
0.546 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252068 |
|
|
Mus musculus |
|
pmid |
sentence |
17667936 |
SARM utilizes its TIR domain to negatively regulate TRIF |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | Toll like receptors |
+ |
TICAM1 | up-regulates activity
binding
|
TBK1 |
0.814 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-118458 |
|
|
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
14530355 |
Toll/il-1 receptor domain-containing adaptor inducing ifn-beta (trif) associates with tnf receptor-associated factor 6 and tank-binding kinase 1, and activates two distinct transcription factors, nf-kappa b and ifn-regulatory factor-3, in the toll-like receptor signaling |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, EBV infection, Innate Immune Response, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE, SARS-CoV INNATE RESPONSE TO dsRNA, Toll like receptors |
+ |
TICAM2 | up-regulates activity
binding
|
TICAM1 |
0.568 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-118367 |
|
|
Homo sapiens |
Macrophage |
pmid |
sentence |
14519765 |
Tram binds trif directly and recruits it to tlr4 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Macrophage polarization, Toll like receptors |
+ |
TLRs | up-regulates activity
binding
|
TICAM1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252095 |
|
|
Mus musculus |
|
pmid |
sentence |
22664090 |
To initiate the innate immune response, Toll-like receptors (TLRs) associate with cytoplasmic adaptor proteins through TIR (Toll/interleukin-1 receptor) domain interactions. The four principal signaling adaptor proteins include MyD88, MAL, TRIF and TRAM, and the fifth protein SARM, involved in negative regulation of TLR pathways, is usually considered a part of the TIR domain-containing adaptor protein group |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | COVID-19 Causal Network, Innate Immune Response, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE, Toll like receptors |
+ |
TRAF6 | up-regulates
polyubiquitination
|
TICAM1 |
0.823 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-271428 |
|
|
Homo sapiens |
|
pmid |
sentence |
20047764 |
Here, we show that the TRAF family proteins directly bind TICAM-1 and demonstrate that TRAF2 and TRAF6 bind different sites of the N-terminal TICAM-1 and accelerate its polyubiquitination. we speculate that polyubiquitination of TICAM-1 by TRAF2 and TRAF6 is required for TICAM-1 to induce IRF-3 and NF-κB activation. This is supported by the observation that polyubiquitination of TICAM-1 was required for TRAF3-binding to TICAM-1 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, EBV infection, Innate Immune Response, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE, Toll like receptors |