Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0117 | 1 | 1 |
Brugia malayi | endochitinase | 0.0082 | 0.3645 | 0.2052 |
Onchocerca volvulus | 0.0117 | 1 | 1 | |
Leishmania major | chitinase | 0.0073 | 0.2004 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Onchocerca volvulus | 0.0117 | 1 | 1 | |
Mycobacterium ulcerans | chitinase/cellulase | 0.0063 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0117 | 1 | 1 |
Mycobacterium ulcerans | chitinase/cellulase | 0.0063 | 0 | 0.5 |
Entamoeba histolytica | chitinase, putative | 0.0073 | 0.2004 | 0.5 |
Plasmodium vivax | hypothetical protein, conserved | 0.0117 | 1 | 0.5 |
Brugia malayi | Endochitinase | 0.0082 | 0.3645 | 0.2052 |
Toxoplasma gondii | hypothetical protein | 0.0117 | 1 | 0.5 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0073 | 0.2004 | 0.2004 |
Loa Loa (eye worm) | chitinase I | 0.0073 | 0.2004 | 0.2004 |
Plasmodium falciparum | conserved protein, unknown function | 0.0117 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0063 | 0 | 0.5 |
Echinococcus multilocularis | Hepatocellular carcinoma associated antigen 59 | 0.0117 | 1 | 0.5 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0072 | 0.1641 | 0.1641 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Onchocerca volvulus | Putative endochitinase | 0.0082 | 0.3645 | 0.2052 |
Echinococcus granulosus | Hepatocellular carcinoma associated antigen 59 | 0.0117 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0117 | 1 | 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.