Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | protease, serine, 3 | Starlite/ChEMBL | References |
Homo sapiens | kallikrein B, plasma (Fletcher factor) 1 | Starlite/ChEMBL | References |
Homo sapiens | protease, serine, 2 (trypsin 2) | References | |
Homo sapiens | protease, serine, 1 (trypsin 1) | References | |
Homo sapiens | coagulation factor VII (serum prothrombin conversion accelerator) | Starlite/ChEMBL | References |
Homo sapiens | plasminogen activator, tissue | Starlite/ChEMBL | References |
Homo sapiens | plasminogen activator, urokinase | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Echinococcus granulosus | glycoprotein Antigen 5 | coagulation factor VII (serum prothrombin conversion accelerator) | 466 aa | 384 aa | 23.7 % |
Brugia malayi | Trypsin family protein | protease, serine, 1 (trypsin 1) | 247 aa | 287 aa | 21.6 % |
Echinococcus granulosus | Mastin | plasminogen activator, urokinase | 414 aa | 340 aa | 24.4 % |
Schistosoma mansoni | cercarial elastase (S01 family) | protease, serine, 3 | 261 aa | 234 aa | 25.2 % |
Schistosoma mansoni | cercarial elastase (S01 family) | protease, serine, 2 (trypsin 2) | 247 aa | 240 aa | 25.8 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0358 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0358 | 1 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0356 | 0.956 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0356 | 0.956 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0358 | 1 | 0.5 |
Onchocerca volvulus | 0.0358 | 1 | 1 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0358 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 0.36 uM | The compound was tested for inhibition of human urokinase type plasminogen activator (microPa) | ChEMBL. | 11689072 |
Ki (binding) | = 0.36 uM | The compound was tested for inhibition of human urokinase type plasminogen activator (microPa) | ChEMBL. | 11689072 |
Ki (binding) | = 0.6 uM | The compound was tested for inhibition of human p-kallikrein | ChEMBL. | 11689072 |
Ki (binding) | = 0.6 uM | The compound was tested for inhibition of human p-kallikrein | ChEMBL. | 11689072 |
Ki (binding) | = 3.9 uM | The compound was tested for inhibition of human plasmin | ChEMBL. | 11689072 |
Ki (binding) | = 3.9 uM | The compound was tested for inhibition of human plasmin | ChEMBL. | 11689072 |
Ki (binding) | = 14 uM | The compound was tested for inhibition of human trypsin | ChEMBL. | 11689072 |
Ki (binding) | = 14 uM | The compound was tested for inhibition of human trypsin | ChEMBL. | 11689072 |
Ki (binding) | = 16 uM | The compound was tested for inhibition of human coagulation factor VII | ChEMBL. | 11689072 |
Ki (binding) | = 16 uM | The compound was tested for inhibition of human coagulation factor VII | ChEMBL. | 11689072 |
Ki (binding) | = 18 uM | The compound was tested for inhibition of human tissue plasminogen activator | ChEMBL. | 11689072 |
Ki (binding) | = 18 uM | The compound was tested for inhibition of human tissue plasminogen activator | ChEMBL. | 11689072 |
Ki (binding) | = 26 uM | Binding affinity against human coagulation factor X | ChEMBL. | 11689072 |
Ki (binding) | = 26 uM | Binding affinity against human coagulation factor X | ChEMBL. | 11689072 |
Ki (binding) | > 75 uM | The compound was tested for inhibition of human thrombin | ChEMBL. | 11689072 |
Ki (binding) | > 75 uM | The compound was tested for inhibition of human thrombin | ChEMBL. | 11689072 |
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.