Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0112 | 0 | 0.5 |
Entamoeba histolytica | tyrosin kinase, putative | 0.015 | 0.035 | 1 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0255 | 0.1308 | 0.2401 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0112 | 0 | 0.5 |
Echinococcus multilocularis | semaphorin 5B | 0.0255 | 0.1308 | 0.2401 |
Echinococcus multilocularis | plexin a4 | 0.0709 | 0.5448 | 1 |
Onchocerca volvulus | Tyrosine kinase homolog | 0.02 | 0.0799 | 0.1103 |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Entamoeba histolytica | protein kinase domain containing protein | 0.015 | 0.035 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0112 | 0 | 0.5 |
Schistosoma mansoni | plexin | 0.0597 | 0.4428 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Onchocerca volvulus | 0.0597 | 0.4428 | 1 | |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Brugia malayi | Immunoglobulin I-set domain containing protein | 0.0252 | 0.1275 | 0.2341 |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Echinococcus granulosus | semaphorin 5B | 0.0255 | 0.1308 | 0.1308 |
Loa Loa (eye worm) | hypothetical protein | 0.0597 | 0.4428 | 0.8127 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Brugia malayi | Sema domain containing protein | 0.0255 | 0.1308 | 0.2401 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0255 | 0.1308 | 0.2401 |
Brugia malayi | Sema domain containing protein | 0.0255 | 0.1308 | 0.2401 |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Echinococcus granulosus | semaphorin 1A | 0.0255 | 0.1308 | 0.1308 |
Schistosoma mansoni | plexin | 0.0342 | 0.2099 | 0.4741 |
Schistosoma mansoni | hypothetical protein | 0.0255 | 0.1308 | 0.2955 |
Loa Loa (eye worm) | hypothetical protein | 0.0342 | 0.2099 | 0.3853 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0112 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Echinococcus granulosus | plexin a4 | 0.0709 | 0.5448 | 0.5448 |
Echinococcus multilocularis | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Brugia malayi | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Trichomonas vaginalis | Clan MA, family M8, leishmanolysin-like metallopeptidase | 0.0112 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Schistosoma mansoni | semaphorin 5-related | 0.0255 | 0.1308 | 0.2955 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0112 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Schistosoma mansoni | hypothetical protein | 0.0342 | 0.2099 | 0.4741 |
Onchocerca volvulus | 0.0255 | 0.1308 | 0.2351 | |
Brugia malayi | hypothetical protein | 0.0255 | 0.1308 | 0.2401 |
Loa Loa (eye worm) | plexin A | 0.0709 | 0.5448 | 1 |
Brugia malayi | Plexin repeat family protein | 0.0597 | 0.4428 | 0.8127 |
Schistosoma mansoni | hypothetical protein | 0.0255 | 0.1308 | 0.2955 |
Loa Loa (eye worm) | TK/KIN16 protein kinase | 0.0252 | 0.1275 | 0.2341 |
Brugia malayi | plexin A | 0.0709 | 0.5448 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IZ (functional) | = 7 mm | Antibacterial activity against Escherichia coli ATCC 35218 assessed as growth inhibition at 10 ug/mL after 24 hr by agar disc diffusion method | ChEMBL. | No reference |
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.