Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium tuberculosis | Divalent cation-transport integral membrane protein MntH (BRAMP) (MRAMP) | 0.0321 | 0 | 0.5 |
Mycobacterium ulcerans | manganese transport protein MntH | 0.0519 | 1 | 0.5 |
Schistosoma mansoni | divalent metal transporter DMT1B | 0.0519 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0519 | 1 | 0.5 |
Schistosoma mansoni | divalent metal transporter DMT1B | 0.0519 | 1 | 0.5 |
Toxoplasma gondii | divalent metal transporter, putative | 0.0519 | 1 | 0.5 |
Onchocerca volvulus | Protein Malvolio homolog | 0.0519 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0519 | 1 | 0.5 |
Plasmodium vivax | metal transporter, putative | 0.0519 | 1 | 0.5 |
Plasmodium falciparum | transporter, putative | 0.0519 | 1 | 0.5 |
Mycobacterium leprae | DIVALENT CATION-TRANSPORT INTEGRAL MEMBRANE PROTEIN MNTH (BRAMP) (MRAMP) | 0.0321 | 0 | 0.5 |
Echinococcus granulosus | divalent metal transporter DMT1B | 0.0519 | 1 | 0.5 |
Echinococcus multilocularis | divalent metal transporter DMT1B | 0.0519 | 1 | 0.5 |
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.