Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | serotonin transporter b | 0.226 | 1 | 1 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0384 | 0 | 0.5 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.226 | 1 | 0.5 |
Loa Loa (eye worm) | norepinephrine transporter | 0.226 | 1 | 1 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0384 | 0 | 0.5 |
Toxoplasma gondii | hypothetical protein | 0.0384 | 0 | 0.5 |
Onchocerca volvulus | 0.226 | 1 | 1 | |
Loa Loa (eye worm) | hypothetical protein | 0.226 | 1 | 1 |
Plasmodium falciparum | amino acid transporter, putative | 0.0384 | 0 | 0.5 |
Plasmodium falciparum | transporter, putative | 0.0384 | 0 | 0.5 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.226 | 1 | 1 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0384 | 0 | 0.5 |
Echinococcus multilocularis | serotonin transporter | 0.226 | 1 | 1 |
Plasmodium vivax | hypothetical protein, conserved | 0.0384 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.226 | 1 | 1 |
Echinococcus granulosus | serotonin transporter | 0.226 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.226 | 1 | 1 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.226 | 1 | 1 |
Toxoplasma gondii | hypothetical protein | 0.0384 | 0 | 0.5 |
Plasmodium vivax | amine transporter, putative | 0.0384 | 0 | 0.5 |
Chlamydia trachomatis | Ssodium-dependent amino acid transporter | 0.0384 | 0 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.226 | 1 | 1 |
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.