Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | hypothetical protein | 0.0204 | 0.9996 | 0.9996 |
Echinococcus granulosus | serine:threonine protein kinase PLK1 | 0.0107 | 0.4729 | 0.4729 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Trypanosoma cruzi | polo-like protein kinase, putative | 0.0107 | 0.4729 | 0.9833 |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0026 | 0.0264 | 0.0264 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0053 | 0.1786 | 0.3777 |
Brugia malayi | MH2 domain containing protein | 0.0078 | 0.3153 | 0.6557 |
Loa Loa (eye worm) | hypothetical protein | 0.0039 | 0.1001 | 0.1001 |
Leishmania major | serine/threonine-protein kinase, putative,protein kinase, putative | 0.0109 | 0.4809 | 1 |
Loa Loa (eye worm) | CMGC/DYRK/DYRK1 protein kinase | 0.0109 | 0.4809 | 0.4809 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0026 | 0.0264 | 0.0264 |
Echinococcus multilocularis | lysosomal alpha glucosidase | 0.0093 | 0.396 | 0.396 |
Trypanosoma cruzi | CMGC/DYRK protein kinase, putative | 0.0109 | 0.4809 | 1 |
Entamoeba histolytica | protein kinase domain containing protein | 0.0109 | 0.4809 | 1 |
Onchocerca volvulus | Serine\/threonine kinase homolog | 0.0107 | 0.4729 | 1 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Trypanosoma brucei | polo-like protein kinase | 0.0107 | 0.4729 | 0.9833 |
Schistosoma mansoni | hypothetical protein | 0.0204 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0108 | 0.4759 | 0.4759 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0053 | 0.1786 | 0.3777 |
Echinococcus granulosus | dual specificity | 0.0109 | 0.4809 | 0.4809 |
Loa Loa (eye worm) | MH2 domain-containing protein | 0.0078 | 0.3153 | 0.3153 |
Echinococcus granulosus | lysosomal alpha glucosidase | 0.0093 | 0.396 | 0.396 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0204 | 1 | 1 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Loa Loa (eye worm) | transcription factor SMAD2 | 0.0078 | 0.3153 | 0.3153 |
Entamoeba histolytica | protein kinase, putative | 0.0109 | 0.4809 | 1 |
Entamoeba histolytica | protein kinase, putative | 0.0109 | 0.4809 | 1 |
Echinococcus multilocularis | lysosomal alpha glucosidase | 0.0093 | 0.396 | 0.396 |
Schistosoma mansoni | alpha-glucosidase | 0.008 | 0.3251 | 0.3251 |
Loa Loa (eye worm) | hypothetical protein | 0.0108 | 0.4759 | 0.4759 |
Loa Loa (eye worm) | hypothetical protein | 0.0204 | 1 | 1 |
Echinococcus multilocularis | geminin | 0.0204 | 0.9996 | 0.9996 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0107 | 0.4729 | 0.4729 |
Echinococcus granulosus | geminin | 0.0204 | 0.9996 | 0.9996 |
Brugia malayi | GTP-binding regulatory protein Gs alpha-S chain, putative | 0.0026 | 0.0264 | 0.0548 |
Brugia malayi | serine/threonine-protein kinase plk-2 | 0.0107 | 0.4729 | 0.9833 |
Trypanosoma cruzi | polo-like protein kinase, putative | 0.0107 | 0.4729 | 0.9833 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0026 | 0.0264 | 0.0264 |
Brugia malayi | Protein kinase domain containing protein | 0.0109 | 0.4809 | 1 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Brugia malayi | Glycosyl hydrolases family 31 protein | 0.0093 | 0.396 | 0.8235 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Schistosoma mansoni | alpha-glucosidase | 0.008 | 0.3251 | 0.3251 |
Loa Loa (eye worm) | hypothetical protein | 0.0074 | 0.2919 | 0.2919 |
Trypanosoma cruzi | CMGC/DYRK protein kinase, putative | 0.0109 | 0.4809 | 1 |
Schistosoma mansoni | calcium-activated potassium channel | 0.0157 | 0.7431 | 0.7431 |
Entamoeba histolytica | hypothetical protein | 0.0109 | 0.4809 | 1 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Loa Loa (eye worm) | glycosyl hydrolase family 31 protein | 0.0093 | 0.396 | 0.396 |
Schistosoma mansoni | kinase | 0.0055 | 0.1863 | 0.1863 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0026 | 0.0264 | 0.0264 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0026 | 0.0264 | 0.0264 |
Giardia lamblia | Kinase, PLK | 0.0107 | 0.4729 | 0.5 |
Leishmania major | protein kinase, putative,polo-like protein kinase, putative | 0.0107 | 0.4729 | 0.9833 |
Toxoplasma gondii | glycosyl hydrolase, family 31 protein | 0.0021 | 0 | 0.5 |
Echinococcus multilocularis | serine:threonine protein kinase PLK1 | 0.0107 | 0.4729 | 0.4729 |
Entamoeba histolytica | serine/threonine protein kinase, putative | 0.0107 | 0.4729 | 0.9833 |
Loa Loa (eye worm) | hypothetical protein | 0.0083 | 0.3382 | 0.3382 |
Loa Loa (eye worm) | GTP-binding regulatory protein Gs alpha-S chain | 0.0026 | 0.0264 | 0.0264 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0026 | 0.0264 | 0.0264 |
Schistosoma mansoni | serine/threonine protein kinase | 0.0109 | 0.4809 | 0.4809 |
Echinococcus multilocularis | dual specificity | 0.0109 | 0.4809 | 0.4809 |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0026 | 0.0264 | 0.0264 |
Schistosoma mansoni | hypothetical protein | 0.0204 | 0.9996 | 0.9996 |
Trichomonas vaginalis | CAMK family protein kinase | 0.0107 | 0.4729 | 1 |
Loa Loa (eye worm) | PLK/PLK1 protein kinase | 0.0107 | 0.4729 | 0.4729 |
Trypanosoma brucei | CMGC/DYRK protein kinase, putative | 0.0109 | 0.4809 | 1 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.0204 | 1 | 1 |
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.