+ |
Caspase 1 complex | up-regulates activity
cleavage
|
IL1B |
0.796 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256376 |
Asp116 |
DNEAYVHdAPVRSLN |
in vitro |
|
pmid |
sentence |
1919001 |
IL-1 converting enzyme (ICE) specifically cleaves the human IL-1 beta precursor at two sequence-related sites: Asp27-Gly28 (site 1) and Asp116-Ala117 (site 2). Cleavage at Asp116-Ala117 results in the generation of mature, biologically active IL-1 beta. |
|
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256375 |
Asp27 |
DDLFFEAdGPKQMKC |
in vitro |
|
pmid |
sentence |
1919001 |
IL-1 converting enzyme (ICE) specifically cleaves the human IL-1 beta precursor at two sequence-related sites: Asp27-Gly28 (site 1) and Asp116-Ala117 (site 2). Cleavage at Asp116-Ala117 results in the generation of mature, biologically active IL-1 beta. |
|
Publications: |
2 |
Organism: |
In Vitro |
Pathways: | COVID-19 Causal Network, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE |
+ |
Caspase 1 complex | up-regulates activity
cleavage
|
GSDMD |
0.634 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256415 |
Asp275 |
CLHNFLTdGVPAEGA |
Homo sapiens |
HEK-293 Cell |
pmid |
sentence |
26375003 |
Co-expression of GSDMD with caspase-1, 4, 5 or 11 but not apoptotic caspases (caspase-2, 8 and 9) in 293T cells induced the same cleavage of GSDMD|inflammatory caspases specifically cleave GSDMD after the 272FLTD275 (or 273LLSD276) sequence | |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | Inflammosome Activation |
+ |
Caspase 1 complex | up-regulates activity
cleavage
|
IL18 |
0.784 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256377 |
Asp36 |
DDENLESdYFGKLES |
Homo sapiens |
THP-1 Cell |
pmid |
sentence |
9334240 |
We also found two precursor hIL-18 (prohIL-18)-processing activities in the cytosol of THP.1 cells. These activities were blocked separately by the caspase inhibitors Ac-YVAD-CHO and Ac-DEVD-CHO. Further analyses of the partially purified enzymes revealed that one is caspase-1, which cleaves prohIL-18 at the Asp36-Tyr37 site to generate the mature hIL-18, and the other is caspase-3, which cleaves both precursor and mature hIL-18 at Asp71-Ser72 and Asp76-Asn77 to generate biologically inactive products. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | COVID-19 Causal Network, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE |
+ |
CASP1 | form complex
binding
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256386 |
|
|
|
|
pmid |
sentence |
7721861 |
The interleukin-1 beta-converting enzyme is a heterodimeric cysteine protease that is produced as a 45-kDa precursor. The full-length precursor form of the enzyme was expressed in Escherichia coli as insoluble inclusion bodies. Following solubilization and refolding of the 45-kDa protein, autoproteolytic conversion to a heterodimeric form containing 10- and 20-kDa subunits was observed. |
|
Publications: |
1 |
+ |
NLRP1 inflammasome | up-regulates activity
cleavage
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256380 |
|
|
|
|
pmid |
sentence |
30288079 |
Canonical inflammasomes form activation platforms for caspase-1. Their assembly depends on some dedicated cytosolic PRRs from the nucleotide-binding domain leucin-rich repeat (NLR) family including NLR and pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR and caspase recruitment domain containing receptor 4 (NLRC4); the AIM2-like receptors (ALR) family including absent in melanoma 2 (AIM2); or the tripartite motif (TRIM) family including pyrin. |
|
Publications: |
1 |
Pathways: | Inflammosome Activation |
+ |
Pyrin inflammasome | up-regulates activity
cleavage
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256383 |
|
|
|
|
pmid |
sentence |
30288079 |
Canonical inflammasomes form activation platforms for caspase-1. Their assembly depends on some dedicated cytosolic PRRs from the nucleotide-binding domain leucin-rich repeat (NLR) family including NLR and pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR and caspase recruitment domain containing receptor 4 (NLRC4); the AIM2-like receptors (ALR) family including absent in melanoma 2 (AIM2); or the tripartite motif (TRIM) family including pyrin. |
|
Publications: |
1 |
+ |
NLRP3 inflammasome | up-regulates activity
cleavage
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256381 |
|
|
|
|
pmid |
sentence |
30288079 |
Canonical inflammasomes form activation platforms for caspase-1. Their assembly depends on some dedicated cytosolic PRRs from the nucleotide-binding domain leucin-rich repeat (NLR) family including NLR and pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR and caspase recruitment domain containing receptor 4 (NLRC4); the AIM2-like receptors (ALR) family including absent in melanoma 2 (AIM2); or the tripartite motif (TRIM) family including pyrin. |
|
Publications: |
1 |
Pathways: | COVID-19 Causal Network, Inflammosome Activation, SARS-CoV INFLAMMATORY RESPONSE |
+ |
NLRC4 inflammasome | up-regulates activity
cleavage
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256384 |
|
|
|
|
pmid |
sentence |
30288079 |
Canonical inflammasomes form activation platforms for caspase-1. Their assembly depends on some dedicated cytosolic PRRs from the nucleotide-binding domain leucin-rich repeat (NLR) family including NLR and pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR and caspase recruitment domain containing receptor 4 (NLRC4); the AIM2-like receptors (ALR) family including absent in melanoma 2 (AIM2); or the tripartite motif (TRIM) family including pyrin. |
|
Publications: |
1 |
Pathways: | Inflammosome Activation |
+ |
AIM2 inflammasome | up-regulates activity
cleavage
|
Caspase 1 complex |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256382 |
|
|
|
|
pmid |
sentence |
30288079 |
Canonical inflammasomes form activation platforms for caspase-1. Their assembly depends on some dedicated cytosolic PRRs from the nucleotide-binding domain leucin-rich repeat (NLR) family including NLR and pyrin domain containing receptor 1 (NLRP1), NLRP3, and NLR and caspase recruitment domain containing receptor 4 (NLRC4); the AIM2-like receptors (ALR) family including absent in melanoma 2 (AIM2); or the tripartite motif (TRIM) family including pyrin. |
|
Publications: |
1 |
Pathways: | Inflammosome Activation |