Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Plasmodium vivax | hypothetical protein, conserved | 0.0088 | 0 | 0.5 |
Echinococcus multilocularis | serotonin transporter | 0.052 | 1 | 1 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0088 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.052 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.052 | 1 | 1 |
Onchocerca volvulus | 0.052 | 1 | 1 | |
Plasmodium falciparum | transporter, putative | 0.0088 | 0 | 0.5 |
Schistosoma mansoni | norepinephrine/norepinephrine transporter | 0.052 | 1 | 1 |
Plasmodium falciparum | amino acid transporter, putative | 0.0088 | 0 | 0.5 |
Treponema pallidum | sodium- and chloride- dependent transporter | 0.052 | 1 | 0.5 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0088 | 0 | 0.5 |
Toxoplasma gondii | hypothetical protein | 0.0088 | 0 | 0.5 |
Loa Loa (eye worm) | norepinephrine transporter | 0.052 | 1 | 1 |
Toxoplasma gondii | Sodium:neurotransmitter symporter family protein | 0.0088 | 0 | 0.5 |
Loa Loa (eye worm) | serotonin transporter b | 0.052 | 1 | 1 |
Plasmodium vivax | amine transporter, putative | 0.0088 | 0 | 0.5 |
Schistosoma mansoni | sodium/chloride dependent transporter | 0.052 | 1 | 1 |
Chlamydia trachomatis | Ssodium-dependent amino acid transporter | 0.0088 | 0 | 0.5 |
Toxoplasma gondii | hypothetical protein | 0.0088 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.052 | 1 | 1 |
Echinococcus granulosus | serotonin transporter | 0.052 | 1 | 1 |
Loa Loa (eye worm) | solute carrier family 6 member 4 | 0.052 | 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.