Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium tuberculosis | 3-oxoacyl-[acyl-carrier-protein] synthase III FabH (beta-ketoacyl-ACP synthase III) (KAS III) | 0.5663 | 1 | 0.5 |
Plasmodium falciparum | beta-ketoacyl-ACP synthase III | 0.5663 | 1 | 0.5 |
Echinococcus multilocularis | insulin growth factor 1 receptor beta | 0.107 | 0.0073 | 0.0145 |
Brugia malayi | Furin-like cysteine rich region family protein | 0.335 | 0.5 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.1781 | 0.1608 | 0.3117 |
Echinococcus multilocularis | epidermal growth factor receptor | 0.335 | 0.5 | 1 |
Mycobacterium ulcerans | beta-ketoacyl synthase-like protein | 0.5663 | 1 | 0.5 |
Schistosoma mansoni | tyrosine kinase | 0.18 | 0.1649 | 0.32 |
Schistosoma mansoni | tyrosine kinase | 0.1781 | 0.1608 | 0.3117 |
Mycobacterium ulcerans | 3-oxoacyl-ACP synthase | 0.5663 | 1 | 0.5 |
Schistosoma mansoni | tyrosine kinase | 0.335 | 0.5 | 1 |
Echinococcus granulosus | epidermal growth factor receptor | 0.18 | 0.1649 | 0.32 |
Echinococcus granulosus | melanoma receptor tyrosine protein kinase | 0.18 | 0.1649 | 0.32 |
Mycobacterium ulcerans | 3-oxoacyl-ACP synthase | 0.5663 | 1 | 0.5 |
Schistosoma mansoni | tyrosine kinase | 0.18 | 0.1649 | 0.32 |
Echinococcus granulosus | epidermal growth factor receptor | 0.335 | 0.5 | 1 |
Loa Loa (eye worm) | TK/EGFR protein kinase | 0.335 | 0.5 | 1 |
Schistosoma mansoni | tyrosine kinase | 0.1781 | 0.1608 | 0.3117 |
Plasmodium vivax | beta-ketoacyl-acyl carrier protein synthase III precursor, putative | 0.5663 | 1 | 0.5 |
Echinococcus multilocularis | epidermal growth factor receptor | 0.18 | 0.1649 | 0.3299 |
Wolbachia endosymbiont of Brugia malayi | 3-oxoacyl-ACP synthase | 0.5663 | 1 | 0.5 |
Echinococcus multilocularis | insulin receptor | 0.107 | 0.0073 | 0.0145 |
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.