Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Brugia malayi | Lipocalin / cytosolic fatty-acid binding protein family protein | 0.0258 | 0.4384 | 0.4384 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.0187 | 0.296 | 0.5 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | Dopamine\/Ecdysteroid receptor homolog | 0.0039 | 0 | 0.5 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Loa Loa (eye worm) | TK/FAK protein kinase | 0.0539 | 1 | 1 |
Echinococcus granulosus | protein tyrosine kinase | 0.0533 | 0.9874 | 1 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.0187 | 0.296 | 0.5 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Schistosoma mansoni | tyrosine kinase | 0.0533 | 0.9874 | 1 |
Echinococcus multilocularis | protein tyrosine kinase | 0.0533 | 0.9874 | 1 |
Loa Loa (eye worm) | lipocalin/cytosolic fatty-acid binding protein family protein | 0.0258 | 0.4384 | 0.4384 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | Neuropeptide F receptor homolog | 0.0039 | 0 | 0.5 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Mycobacterium tuberculosis | Probable flavin-containing monoamine oxidase AofH (amine oxidase) (MAO) | 0.0174 | 0.2697 | 0.5 |
Onchocerca volvulus | 0.0039 | 0 | 0.5 | |
Onchocerca volvulus | 0.0039 | 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.