Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma cruzi | dihydrofolate reductase-thymidylate synthase, putative | 0.1169 | 0.4189 | 0.4186 |
Echinococcus granulosus | DNA apurinic or apyrimidinic site lyase | 0.0012 | 0.0006 | 0.0007 |
Echinococcus multilocularis | jumonji domain containing protein | 0.0026 | 0.0057 | 0.0065 |
Schistosoma mansoni | jumonji domain containing protein | 0.0048 | 0.0138 | 0.0156 |
Mycobacterium tuberculosis | Probable glutamine-binding lipoprotein GlnH (GLNBP) | 0.0017 | 0.0025 | 0.0022 |
Loa Loa (eye worm) | hypothetical protein | 0.0019 | 0.0031 | 0.0028 |
Toxoplasma gondii | PHD-finger domain-containing protein | 0.0019 | 0.0031 | 0.0025 |
Schistosoma mansoni | ap endonuclease | 0.0012 | 0.0006 | 0.0007 |
Echinococcus multilocularis | PHD finger protein rhinoceros | 0.0019 | 0.0031 | 0.0035 |
Brugia malayi | hypothetical protein | 0.1169 | 0.4189 | 0.4732 |
Brugia malayi | Dihydrofolate reductase | 0.0835 | 0.2983 | 0.3367 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0022 | 0.0045 | 0.0044 |
Schistosoma mansoni | ap endonuclease | 0.0012 | 0.0006 | 0.0007 |
Echinococcus multilocularis | DNA (apurinic or apyrimidinic site) lyase | 0.0012 | 0.0006 | 0.0007 |
Mycobacterium ulcerans | dihydrofolate reductase DfrA | 0.0835 | 0.2983 | 0.3367 |
Brugia malayi | thymidylate synthase | 0.2457 | 0.8846 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0019 | 0.0031 | 0.0035 |
Echinococcus multilocularis | thymidylate synthase | 0.2457 | 0.8846 | 1 |
Echinococcus granulosus | jumonji domain containing protein | 0.0026 | 0.0057 | 0.0065 |
Echinococcus granulosus | tm gpcr rhodopsin | 0.0137 | 0.0459 | 0.0519 |
Echinococcus granulosus | Transcription factor JmjC domain containing protein | 0.0061 | 0.0183 | 0.0207 |
Echinococcus multilocularis | peregrin | 0.0019 | 0.0031 | 0.0035 |
Toxoplasma gondii | PHD-finger domain-containing protein | 0.0019 | 0.0031 | 0.0025 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.0079 | 0.0082 |
Loa Loa (eye worm) | dihydrofolate reductase | 0.0835 | 0.2983 | 0.3367 |
Brugia malayi | jmjC domain containing protein | 0.0061 | 0.0183 | 0.02 |
Mycobacterium ulcerans | thymidylate synthase | 0.2457 | 0.8846 | 1 |
Echinococcus granulosus | lysine specific demethylase 5A | 0.0022 | 0.0045 | 0.0051 |
Echinococcus granulosus | peregrin | 0.0019 | 0.0031 | 0.0035 |
Wolbachia endosymbiont of Brugia malayi | exonuclease III | 0.0012 | 0.0006 | 0.5 |
Loa Loa (eye worm) | transcription factor SMAD2 | 0.0074 | 0.023 | 0.0254 |
Plasmodium falciparum | phd finger protein, putative | 0.0019 | 0.0031 | 0.0025 |
Echinococcus multilocularis | tm gpcr rhodopsin gpcr rhodopsin superfamily | 0.0137 | 0.0459 | 0.0519 |
Mycobacterium tuberculosis | Hypothetical protein | 0.1169 | 0.4189 | 0.4732 |
Treponema pallidum | amino acid ABC transporter, periplasmic binding protein (hisJ) | 0.0017 | 0.0025 | 1 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0022 | 0.0045 | 0.0051 |
Brugia malayi | PHD-finger family protein | 0.0019 | 0.0031 | 0.0028 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0022 | 0.0045 | 0.0051 |
Echinococcus multilocularis | nmda type glutamate receptor | 0.0023 | 0.0049 | 0.0055 |
Echinococcus granulosus | thymidylate synthase | 0.2457 | 0.8846 | 1 |
Chlamydia trachomatis | dihydrofolate reductase | 0.0835 | 0.2983 | 1 |
Mycobacterium ulcerans | glutamine-binding lipoprotein GlnH | 0.0017 | 0.0025 | 0.0022 |
Brugia malayi | jmjC domain containing protein | 0.0022 | 0.0045 | 0.0044 |
Echinococcus multilocularis | Glutamate receptor, ionotropic kainate 3 | 0.0023 | 0.0049 | 0.0055 |
Echinococcus granulosus | PHD finger protein rhinoceros | 0.0019 | 0.0031 | 0.0035 |
Echinococcus multilocularis | dihydrofolate reductase | 0.0835 | 0.2983 | 0.3372 |
Mycobacterium leprae | PROBABLE THYMIDYLATE SYNTHASE THYA (TS) (TSASE) | 0.2457 | 0.8846 | 1 |
Mycobacterium tuberculosis | Probable thymidylate synthase ThyA (ts) (TSASE) | 0.2457 | 0.8846 | 1 |
Plasmodium vivax | hypothetical protein, conserved | 0.0019 | 0.0031 | 0.0025 |
Loa Loa (eye worm) | thymidylate synthase | 0.2457 | 0.8846 | 1 |
Loa Loa (eye worm) | MH2 domain-containing protein | 0.0074 | 0.023 | 0.0254 |
Onchocerca volvulus | 0.2457 | 0.8846 | 1 | |
Entamoeba histolytica | exodeoxyribonuclease III, putative | 0.0012 | 0.0006 | 0.5 |
Loa Loa (eye worm) | PHD-finger family protein | 0.0019 | 0.0031 | 0.0028 |
Echinococcus multilocularis | Transcription factor, JmjC domain containing protein | 0.0061 | 0.0183 | 0.0207 |
Schistosoma mansoni | bifunctional dihydrofolate reductase-thymidylate synthase | 0.2457 | 0.8846 | 1 |
Echinococcus granulosus | nmda type glutamate receptor | 0.0023 | 0.0049 | 0.0055 |
Brugia malayi | Bromodomain containing protein | 0.0019 | 0.0031 | 0.0028 |
Schistosoma mansoni | dihydrofolate reductase | 0.0835 | 0.2983 | 0.3372 |
Mycobacterium tuberculosis | Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) | 0.0835 | 0.2983 | 0.3367 |
Mycobacterium tuberculosis | Probable epoxide hydrolase EphA (epoxide hydratase) (arene-oxide hydratase) | 0.0128 | 0.0428 | 0.0477 |
Treponema pallidum | amino acid ABC transporter, periplasmic binding protein | 0.0017 | 0.0025 | 1 |
Brugia malayi | dihydrofolate reductase family protein | 0.0835 | 0.2983 | 0.3367 |
Schistosoma mansoni | bromodomain-containing nuclear protein 1 brd1 | 0.0019 | 0.0031 | 0.0035 |
Giardia lamblia | PHD finger protein 15 | 0.0019 | 0.0031 | 1 |
Echinococcus multilocularis | lysine specific demethylase 5A | 0.0022 | 0.0045 | 0.0051 |
Trichomonas vaginalis | conserved hypothetical protein | 0.1169 | 0.4189 | 1 |
Brugia malayi | MH2 domain containing protein | 0.0074 | 0.023 | 0.0254 |
Mycobacterium ulcerans | epoxide hydrolase EphA | 0.0128 | 0.0428 | 0.0477 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0038 | 0.0102 | 0.0109 |
Echinococcus granulosus | dihydrofolate reductase | 0.0835 | 0.2983 | 0.3372 |
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.