Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | threonyl-tRNA synthetase | 0.0065 | 1 | 1 |
Treponema pallidum | threonyl-tRNA synthetase | 0.0057 | 0.8494 | 1 |
Trypanosoma cruzi | threonyl-tRNA synthetase, putative | 0.0065 | 1 | 1 |
Trichomonas vaginalis | threonyl-tRNA synthetase, putative | 0.0057 | 0.8494 | 1 |
Schistosoma mansoni | threonyl-tRNA synthetase | 0.0052 | 0.7416 | 1 |
Echinococcus granulosus | Threonyl tRNA synthetase C | 0.0065 | 1 | 1 |
Mycobacterium leprae | Probable threonyl-tRNA synthetase ThrS (threonine-tRNA synthetase) (ThrRS) (Threonine-tRNA ligase) | 0.0057 | 0.8494 | 1 |
Plasmodium vivax | threonine--tRNA ligase, putative | 0.0057 | 0.8494 | 1 |
Trypanosoma cruzi | threonyl-tRNA synthetase, putative | 0.0065 | 1 | 1 |
Plasmodium falciparum | threonine--tRNA ligase | 0.0057 | 0.8494 | 1 |
Mycobacterium ulcerans | threonyl-tRNA synthetase | 0.0057 | 0.8494 | 1 |
Leishmania major | threonyl-tRNA synthetase, putative | 0.0065 | 1 | 1 |
Wolbachia endosymbiont of Brugia malayi | threonyl-tRNA synthetase | 0.0057 | 0.8494 | 1 |
Toxoplasma gondii | threonyl-tRNA synthetase family protein | 0.0057 | 0.8494 | 1 |
Trypanosoma brucei | threonyl-tRNA synthetase, putative | 0.0065 | 1 | 1 |
Giardia lamblia | Threonyl-tRNA synthetase | 0.0057 | 0.8494 | 1 |
Mycobacterium tuberculosis | Probable threonyl-tRNA synthetase ThrS (threonine-tRNA synthetase)(ThrRS) (threonine-tRNA ligase) | 0.0057 | 0.8494 | 0.5 |
Entamoeba histolytica | threonyl-tRNA synthetase, putative | 0.0057 | 0.8494 | 1 |
Echinococcus multilocularis | Threonyl tRNA synthetase, C | 0.0065 | 1 | 1 |
Chlamydia trachomatis | threonine--tRNA ligase | 0.0065 | 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.