+ |
TLR2 | up-regulates activity
binding
|
TICAM2 |
0.441 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266747 |
|
|
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 |
+ |
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 |
+ |
TLR2 | up-regulates activity
binding
|
MYD88 |
0.659 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266740 |
|
|
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 |
+ |
TLR2 | down-regulates activity
|
NfKb-p65/p50 |
0.547 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260973 |
|
|
Homo sapiens |
Peripheral Blood Mononuclear Cell |
pmid |
sentence |
19185596 |
S protein is a ligand for human TLR2. S protein utilizes toll-like receptor 2(TLR 2) to increase IL-8 production.Our results show that SARS S protein in a soluble form increased IL-8 production through hTLR2 ligand interaction. we have provided evidence that S protein induces IL-8 in PBMC in vitro and in THP-1 cells. The ability of S protein to increase IL-8 mRNA was mediated by activation of NF-κB possibly via TLR2 ligand and could be inhibited by the NF-κB inhibitor TPCK. The ability to detect elevated NF-κB transcription factor activity in the nucleus in response to S protein suggests that this most likely occurs by the mechanism of induction. Moreover increased secretion of IL-8 and IL-6 cytokines indicated that levels of proinflammatory mediators could be enhanced by S protein interaction with monocyte macrophages and could stimulate NK, neutrophil and monocyte migration to the site of infection. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | EBV infection, SARS-CoV CYTOKINE STORM |
+ |
TLR2 | up-regulates activity
binding
|
TIRAP |
0.716 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266745 |
|
|
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 |
+ |
BGLF5 | down-regulates quantity by repression
post transcriptional regulation
|
TLR2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-266741 |
|
|
Homo sapiens |
HEK-293T Cell |
pmid |
sentence |
26428381 |
The RNA degradation induced by EBV BGLF5 can affect immunologically relevant proteins, including TLR2. Alkaline exonuclease involved in host shutoff, downregulates TLR2. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | EBV infection |
+ |
S | up-regulates activity
binding
|
TLR2 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-260972 |
|
|
Homo sapiens |
Peripheral Blood Mononuclear Cell |
pmid |
sentence |
19185596 |
S protein is a ligand for human TLR2. S protein utilizes toll-like receptor 2(TLR 2) to increase IL-8 production.Our results show that SARS S protein in a soluble form increased IL-8 production through hTLR2 ligand interaction. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | SARS-CoV CYTOKINE STORM |