Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | matrix metallopeptidase 3 (stromelysin 1, progelatinase) | Starlite/ChEMBL | No references |
Homo sapiens | ADAM metallopeptidase domain 9 | Starlite/ChEMBL | No references |
Homo sapiens | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) | Starlite/ChEMBL | No references |
Homo sapiens | ADAM metallopeptidase domain 10 | Starlite/ChEMBL | No references |
Homo sapiens | ADAM metallopeptidase domain 33 | Starlite/ChEMBL | No references |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Brugia malayi | hypothetical protein | ADAM metallopeptidase domain 9 | 819 aa | 733 aa | 29.2 % |
Echinococcus granulosus | matrix metallopeptidase 7 M10 family | matrix metallopeptidase 3 (stromelysin 1, progelatinase) | 477 aa | 431 aa | 34.6 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | disintegrin and metalloproteinase | 0.0146 | 0.6061 | 0.5902 |
Schistosoma mansoni | subfamily M12B unassigned peptidase (M12 family) | 0.0198 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.1237 | 0.0737 |
Echinococcus multilocularis | subfamily M12B unassigned peptidase | 0.0198 | 1 | 1 |
Onchocerca volvulus | Matrix metalloproteinase homolog | 0.0105 | 0.2897 | 1 |
Brugia malayi | ADAMTS-like protease | 0.0083 | 0.1237 | 0.1332 |
Onchocerca volvulus | Matrilysin homolog | 0.0105 | 0.2897 | 1 |
Brugia malayi | hypothetical protein | 0.0189 | 0.9291 | 1 |
Loa Loa (eye worm) | matrixin family protein | 0.0115 | 0.3621 | 0.3257 |
Echinococcus multilocularis | adam | 0.0189 | 0.9291 | 0.8917 |
Brugia malayi | ADAM-TS Spacer 1 family protein | 0.0083 | 0.1237 | 0.1332 |
Brugia malayi | angiogenesis inhibito | 0.0083 | 0.1237 | 0.1332 |
Brugia malayi | Disintegrin family protein | 0.0146 | 0.6061 | 0.6523 |
Echinococcus multilocularis | disintegrin and metalloproteinase | 0.0146 | 0.6061 | 0.3983 |
Loa Loa (eye worm) | matrixin family protein | 0.0105 | 0.2897 | 0.2492 |
Echinococcus granulosus | Blood coagulation inhibitor Disintegrin | 0.0112 | 0.3453 | 0.319 |
Loa Loa (eye worm) | hypothetical protein | 0.0135 | 0.5185 | 0.491 |
Echinococcus multilocularis | matrix metallopeptidase 7 (M10 family) | 0.0172 | 0.8031 | 0.6993 |
Echinococcus granulosus | matrix metallopeptidase 7 M10 family | 0.0172 | 0.8031 | 0.7952 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.1237 | 0.0737 |
Schistosoma mansoni | dihydroceramide desaturase | 0.0146 | 0.6061 | 0.6061 |
Brugia malayi | Matrixin family protein | 0.0115 | 0.3621 | 0.3897 |
Brugia malayi | Reprolysin | 0.0126 | 0.4479 | 0.4821 |
Loa Loa (eye worm) | hypothetical protein | 0.0112 | 0.3453 | 0.308 |
Schistosoma mansoni | subfamily M12B unassigned peptidase (M12 family) | 0.0198 | 1 | 1 |
Echinococcus granulosus | adam | 0.0189 | 0.9291 | 0.9263 |
Schistosoma mansoni | adam (A disintegrin and metalloprotease | 0.0189 | 0.9291 | 0.9291 |
Loa Loa (eye worm) | reprolysin | 0.0198 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 24 nM | BindingDB_Patents: Enzymatic Assay. The products are solubilized in DMSO at a concentration of 10 mM. A serial 3-fold dilution over 10 points is carried out so as to have a concentration range of from 10 uM to 0.5 nM final concentration. The TACE enzyme is an internal production (carried out according to the publication protein Eng Des Sel 2006, 19,155-161) and is added so as to have a signal equivalent to 6 times the background noise in 2 h at 37C. The reaction is carried out in 50 mM Tris buffered medium containing 4% glycerol, pH 7.4. The fluorescent substrate is MCA-Pro-Leu-Ala-Val-(Dpa)-Arg-Ser-Ser-Arg-NH2 (R&D systems, reference: ES003). The substrate is cleaved by the enzyme between the alanine and the valine, thus releasing a fluorescent peptide (excitation: 320 nm, emission: 420 nm). The substrate is used at 40 uM. The reaction is carried out in a final volume of 10 ul (4 ul inhibitor, 4 ul substrate, 2 ul enzyme) in a low volume 384-well plate (Corning reference: 3676). | ChEMBL. | No reference |
IC50 (binding) | = 38 nM | BindingDB_Patents: Enzymatic Assay. The products are solubilized in DMSO at a concentration of 10 mM. A serial 3-fold dilution over 10 points is carried out so as to have a concentration range of from 10 uM to 0.5 nM final concentration. The TACE enzyme is an internal production (carried out according to the publication protein Eng Des Sel 2006, 19,155-161) and is added so as to have a signal equivalent to 6 times the background noise in 2 h at 37C. The reaction is carried out in 50 mM Tris buffered medium containing 4% glycerol, pH 7.4. The fluorescent substrate is MCA-Pro-Leu-Ala-Val-(Dpa)-Arg-Ser-Ser-Arg-NH2 (R&D systems, reference: ES003). The substrate is cleaved by the enzyme between the alanine and the valine, thus releasing a fluorescent peptide (excitation: 320 nm, emission: 420 nm). The substrate is used at 40 uM. The reaction is carried out in a final volume of 10 ul (4 ul inhibitor, 4 ul substrate, 2 ul enzyme) in a low volume 384-well plate (Corning reference: 3676). | ChEMBL. | No reference |
IC50 (binding) | = 3034 nM | Enzymatic Assay | BINDINGDB. | No reference |
IC50 (binding) | > 10000 nM | BindingDB_Patents: Enzymatic Assay. The products are solubilized in DMSO at a concentration of 10 mM. A serial 3-fold dilution over 10 points is carried out so as to have a concentration range of from 10 uM to 0.5 nM final concentration. The TACE enzyme is an internal production (carried out according to the publication protein Eng Des Sel 2006, 19,155-161) and is added so as to have a signal equivalent to 6 times the background noise in 2 h at 37C. The reaction is carried out in 50 mM Tris buffered medium containing 4% glycerol, pH 7.4. The fluorescent substrate is MCA-Pro-Leu-Ala-Val-(Dpa)-Arg-Ser-Ser-Arg-NH2 (R and D systems, reference: ES003). The substrate is cleaved by the enzyme between the alanine and the valine, thus releasing a fluorescent peptide (excitation: 320 nm, emission: 420 nm). The substrate is used at 40 uM. The reaction is carried out in a final volume of 10 ul (4 ul inhibitor, 4 ul substrate, 2 ul enzyme) in a low volume 384-well plate (Corning reference: 3676). | ChEMBL. | No reference |
IC50 (binding) | > 10000 nM | Enzymatic Assay | BINDINGDB. | No reference |
IC50 (binding) | > 10000 nM | Enzymatic Assay | BINDINGDB. | No reference |
IC50 (binding) | > 10000 nM | Enzymatic Assay | BINDINGDB. | No reference |
IC50 (binding) | > 10000 nM | BindingDB_Patents | BINDINGDB. | No reference |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.