Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | coagulation factor II (thrombin) | Starlite/ChEMBL | References |
Homo sapiens | coagulation factor X | Starlite/ChEMBL | References |
Homo sapiens | protease, serine, 1 (trypsin 1) | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Brugia malayi | Trypsin family protein | protease, serine, 1 (trypsin 1) | 247 aa | 287 aa | 21.6 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | hypothetical protein | 0.0255 | 0 | 0.5 |
Echinococcus multilocularis | Peptidase S1 S6, chymotrypsin Hap | 0.0255 | 0 | 0.5 |
Echinococcus granulosus | transmembrane protease serine 3 | 0.0255 | 0 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0529 | 1 | 1 |
Echinococcus multilocularis | subfamily S1A unassigned peptidase (S01 family) | 0.0255 | 0 | 0.5 |
Echinococcus multilocularis | transmembrane protease serine 3 | 0.0255 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0529 | 1 | 1 |
Echinococcus granulosus | subfamily S1A unassigned peptidase S01 family | 0.0255 | 0 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0335 | 0.2932 | 0.5 |
Echinococcus multilocularis | glycoprotein Antigen 5 | 0.0255 | 0 | 0.5 |
Echinococcus granulosus | Peptidase S1 S6 chymotrypsin Hap | 0.0255 | 0 | 0.5 |
Echinococcus granulosus | Mastin | 0.0255 | 0 | 0.5 |
Echinococcus granulosus | glycoprotein Antigen 5 | 0.0255 | 0 | 0.5 |
Echinococcus multilocularis | enteropeptidase | 0.0255 | 0 | 0.5 |
Echinococcus granulosus | enteropeptidase | 0.0255 | 0 | 0.5 |
Onchocerca volvulus | 0.0274 | 0.0686 | 0.0686 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0529 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0529 | 1 | 1 |
Echinococcus multilocularis | Mastin | 0.0255 | 0 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0335 | 0.2932 | 0.5 |
Onchocerca volvulus | 0.0529 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 20 nM | In vitro inhibition of human Coagulation factor X. | ChEMBL. | 10853668 |
Ki (binding) | = 20 nM | In vitro inhibition of human Coagulation factor X. | ChEMBL. | 10853668 |
Ki (binding) | = 30 nM | In vitro inhibition of bovine trypsin. | ChEMBL. | 10853668 |
Ki (binding) | = 30 nM | In vitro inhibition of bovine trypsin. | ChEMBL. | 10853668 |
Ki (binding) | = 2350 nM | In vitro inhibition of human Coagulation factor II. | ChEMBL. | 10853668 |
Ki (binding) | = 2350 nM | In vitro inhibition of human Coagulation factor II. | ChEMBL. | 10853668 |
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.
1 literature reference was collected for this gene.