Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0698 | 0.2382 | 0.2392 |
Loa Loa (eye worm) | hypothetical protein | 0.2004 | 0.9957 | 1 |
Echinococcus granulosus | tissue type plasminogen activator | 0.0698 | 0.2382 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0698 | 0.2382 | 0.2382 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.0698 | 0.2382 | 0.5 |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.0698 | 0.2382 | 0.5 |
Onchocerca volvulus | 0.1717 | 0.8289 | 0.8325 | |
Echinococcus multilocularis | tissue type plasminogen activator | 0.0698 | 0.2382 | 1 |
Brugia malayi | Kringle domain containing protein | 0.0698 | 0.2382 | 0.2392 |
Loa Loa (eye worm) | hypothetical protein | 0.2004 | 0.9957 | 1 |
Mycobacterium ulcerans | hypothetical protein | 0.0288 | 0 | 0.5 |
Brugia malayi | Protein kinase domain containing protein | 0.0698 | 0.2382 | 0.2392 |
Toxoplasma gondii | PAN domain-containing protein | 0.131 | 0.5932 | 1 |
Brugia malayi | Trypsin family protein | 0.2004 | 0.9957 | 1 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0698 | 0.2382 | 0.5 |
Onchocerca volvulus | 0.0698 | 0.2382 | 0.2392 | |
Leishmania major | hypothetical protein, conserved | 0.0698 | 0.2382 | 0.5 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0291 | 0.0022 | 0.0022 |
Onchocerca volvulus | 0.2004 | 0.9957 | 1 | |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.0698 | 0.2382 | 0.2392 |
Toxoplasma gondii | PAN domain-containing protein | 0.131 | 0.5932 | 1 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.2004 | 0.9957 | 0.9957 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
MIC (functional) | = 0.3 mg/ml | Antibacterial activity against Escherichia coli ATCC 25922 after 24 hr by spectrophotometric method | ChEMBL. | No reference |
MIC (functional) | = 10 mg/ml | Antifungal activity against Candida albicans ATCC 10231 after 48 hr by turbidity based microplate metohd | ChEMBL. | 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.