Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | hypothetical protein | 0.0315 | 0.0496 | 0.0496 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.075 | 1 | 1 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.0315 | 0.0496 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.075 | 1 | 1 |
Toxoplasma gondii | PAN domain-containing protein | 0.0726 | 0.9489 | 1 |
Onchocerca volvulus | 0.075 | 1 | 1 | |
Loa Loa (eye worm) | hypothetical protein | 0.0306 | 0.0289 | 0.0289 |
Onchocerca volvulus | 0.0315 | 0.0496 | 0.0496 | |
Echinococcus multilocularis | tissue type plasminogen activator | 0.0315 | 0.0496 | 1 |
Toxoplasma gondii | kringle domain-containing protein | 0.0315 | 0.0496 | 0.0523 |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.0315 | 0.0496 | 0.0496 |
Loa Loa (eye worm) | hypothetical protein | 0.0315 | 0.0496 | 0.0496 |
Brugia malayi | Kringle domain containing protein | 0.0315 | 0.0496 | 0.0496 |
Brugia malayi | Protein kinase domain containing protein | 0.0315 | 0.0496 | 0.0496 |
Loa Loa (eye worm) | hypothetical protein | 0.075 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.075 | 1 | 1 |
Leishmania major | hypothetical protein, conserved | 0.0315 | 0.0496 | 0.5 |
Echinococcus granulosus | tissue type plasminogen activator | 0.0315 | 0.0496 | 1 |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.0315 | 0.0496 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0315 | 0.0496 | 0.5 |
Toxoplasma gondii | PAN domain-containing protein | 0.0726 | 0.9489 | 1 |
Onchocerca volvulus | 0.0583 | 0.635 | 0.635 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
GI (functional) | Antifungal activity against Candida albicans assessed as growth inhibition measured after 24 to 48 hrs by agar disk diffusion method | ChEMBL. | No reference | |
IC50 (binding) | = 99 uM | Inhibitory concentration against Matrix metalloproteinase-3 | ChEMBL. | 10229623 |
IC50 (binding) | = 99 uM | Inhibitory concentration against Matrix metalloproteinase-3 | ChEMBL. | 10229623 |
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.