Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | Hepatocellular carcinoma associated antigen 59 | 0.1343 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.1343 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0848 | 0 | 0.5 |
Echinococcus multilocularis | Hepatocellular carcinoma associated antigen 59 | 0.1343 | 1 | 0.5 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0968 | 0.2426 | 0.2426 |
Onchocerca volvulus | Putative endochitinase | 0.1115 | 0.5389 | 0.3448 |
Onchocerca volvulus | Putative endochitinase | 0.1115 | 0.5389 | 0.3448 |
Entamoeba histolytica | chitinase, putative | 0.0995 | 0.2963 | 0.5 |
Brugia malayi | Endochitinase | 0.1115 | 0.5389 | 0.3448 |
Toxoplasma gondii | hypothetical protein | 0.1343 | 1 | 0.5 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0995 | 0.2963 | 0.2963 |
Plasmodium vivax | hypothetical protein, conserved | 0.1343 | 1 | 0.5 |
Loa Loa (eye worm) | chitinase I | 0.0995 | 0.2963 | 0.2963 |
Plasmodium falciparum | conserved protein, unknown function | 0.1343 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1343 | 1 | 1 |
Brugia malayi | endochitinase | 0.1115 | 0.5389 | 0.3448 |
Leishmania major | chitinase | 0.0995 | 0.2963 | 0.5 |
Onchocerca volvulus | 0.1343 | 1 | 1 | |
Onchocerca volvulus | Putative endochitinase | 0.1115 | 0.5389 | 0.3448 |
Loa Loa (eye worm) | hypothetical protein | 0.1343 | 1 | 1 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0848 | 0 | 0.5 |
Onchocerca volvulus | 0.1343 | 1 | 1 | |
Mycobacterium ulcerans | chitinase/cellulase | 0.0848 | 0 | 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.