Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | chitinase/cellulase | 0.0076 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0141 | 1 | 1 |
Onchocerca volvulus | 0.0141 | 1 | 1 | |
Mycobacterium ulcerans | chitinase/cellulase | 0.0076 | 0 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0099 | 0.3645 | 0.2052 |
Brugia malayi | endochitinase | 0.0099 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | hypothetical protein | 0.0141 | 1 | 1 |
Leishmania major | chitinase | 0.0089 | 0.2004 | 0.5 |
Onchocerca volvulus | 0.0141 | 1 | 1 | |
Plasmodium falciparum | conserved protein, unknown function | 0.0141 | 1 | 0.5 |
Plasmodium vivax | hypothetical protein, conserved | 0.0141 | 1 | 0.5 |
Brugia malayi | Endochitinase | 0.0099 | 0.3645 | 0.2052 |
Toxoplasma gondii | hypothetical protein | 0.0141 | 1 | 0.5 |
Loa Loa (eye worm) | cuticular endochitinase | 0.0089 | 0.2004 | 0.2004 |
Loa Loa (eye worm) | chitinase I | 0.0089 | 0.2004 | 0.2004 |
Entamoeba histolytica | chitinase, putative | 0.0089 | 0.2004 | 0.5 |
Onchocerca volvulus | Putative endochitinase | 0.0099 | 0.3645 | 0.2052 |
Onchocerca volvulus | Putative endochitinase | 0.0099 | 0.3645 | 0.2052 |
Loa Loa (eye worm) | microfilarial chitinase | 0.0086 | 0.1641 | 0.1641 |
Echinococcus multilocularis | Hepatocellular carcinoma associated antigen 59 | 0.0141 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible chitinase | 0.0076 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0141 | 1 | 0.5 |
Echinococcus granulosus | Hepatocellular carcinoma associated antigen 59 | 0.0141 | 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.