Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | lysine specific histone demethylase 1A | 0.0069 | 0.0702 | 0.2596 |
Mycobacterium leprae | PROBABLE PROTOPORPHYRINOGEN OXIDASE HEMY (PROTOPORPHYRINOGEN-IX OXIDASE) (PROTOPORPHYRINOGENASE) (PPO) | 0.0069 | 0.0702 | 0.5 |
Schistosoma mansoni | lipoxygenase | 0.0086 | 0.1008 | 0.1529 |
Loa Loa (eye worm) | hypothetical protein | 0.0069 | 0.0702 | 0.104 |
Schistosoma mansoni | vesicular amine transporter | 0.0185 | 0.2705 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0391 | 0.6253 | 1 |
Mycobacterium tuberculosis | Probable flavin-containing monoamine oxidase AofH (amine oxidase) (MAO) | 0.054 | 0.8821 | 1 |
Brugia malayi | amine oxidase, flavin-containing family protein | 0.008 | 0.09 | 0.1145 |
Plasmodium falciparum | lysine-specific histone demethylase 1, putative | 0.0069 | 0.0702 | 0.5 |
Toxoplasma gondii | histone lysine-specific demethylase | 0.0069 | 0.0702 | 0.5 |
Echinococcus granulosus | lysine specific histone demethylase 1A | 0.0177 | 0.2563 | 0.9476 |
Echinococcus granulosus | arachidonate 5 lipoxygenase | 0.0123 | 0.1648 | 0.6092 |
Mycobacterium ulcerans | flavin-containing monoamine oxidase AofH | 0.0609 | 1 | 1 |
Brugia malayi | hypothetical protein | 0.0069 | 0.0702 | 0.0876 |
Loa Loa (eye worm) | hypothetical protein | 0.02 | 0.2963 | 0.4689 |
Echinococcus multilocularis | arachidonate 5 lipoxygenase | 0.0123 | 0.1648 | 0.6092 |
Toxoplasma gondii | histone lysine-specific demethylase LSD1/BHC110/KDMA1A | 0.0069 | 0.0702 | 0.5 |
Chlamydia trachomatis | protoporphyrinogen oxidase | 0.0069 | 0.0702 | 0.5 |
Plasmodium vivax | lysine-specific histone demethylase 1, putative | 0.0069 | 0.0702 | 0.5 |
Trypanosoma cruzi | C-8 sterol isomerase, putative | 0.0391 | 0.6253 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0188 | 0.2761 | 0.4363 |
Loa Loa (eye worm) | abnormal catecholamine distribution protein 1 | 0.0185 | 0.2705 | 0.4273 |
Onchocerca volvulus | 0.0188 | 0.2761 | 0.5 | |
Echinococcus multilocularis | 0.0069 | 0.0702 | 0.2596 | |
Plasmodium vivax | protoporphyrinogen oxidase, putative | 0.0069 | 0.0702 | 0.5 |
Echinococcus multilocularis | lysine specific histone demethylase 1A | 0.0177 | 0.2563 | 0.9476 |
Plasmodium falciparum | conserved Plasmodium protein, unknown function | 0.0069 | 0.0702 | 0.5 |
Trypanosoma brucei | C-8 sterol isomerase, putative | 0.0391 | 0.6253 | 0.5 |
Echinococcus multilocularis | protoporphyrinogen oxidase | 0.0069 | 0.0702 | 0.2596 |
Brugia malayi | Abnormal catecholamine distribution protein 1 | 0.0185 | 0.2705 | 0.36 |
Echinococcus granulosus | synaptic vesicular amine transporter | 0.0185 | 0.2705 | 1 |
Brugia malayi | SWIRM domain containing protein | 0.0188 | 0.2761 | 0.3676 |
Echinococcus multilocularis | synaptic vesicular amine transporter | 0.0185 | 0.2705 | 1 |
Brugia malayi | Serotonin receptor | 0.0458 | 0.741 | 1 |
Brugia malayi | ERG2 and Sigma1 receptor like protein | 0.0391 | 0.6253 | 0.8426 |
Schistosoma mansoni | Lysine-specific histone demethylase 1 | 0.0177 | 0.2563 | 0.9292 |
Loa Loa (eye worm) | hypothetical protein | 0.0177 | 0.2563 | 0.4044 |
Plasmodium falciparum | protoporphyrinogen oxidase | 0.0069 | 0.0702 | 0.5 |
Schistosoma mansoni | lipoxygenase | 0.0123 | 0.1648 | 0.4721 |
Leishmania major | C-8 sterol isomerase-like protein | 0.0391 | 0.6253 | 1 |
Plasmodium vivax | hypothetical protein, conserved | 0.0069 | 0.0702 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.008 | 0.09 | 0.1359 |
Plasmodium vivax | hypothetical protein, conserved | 0.0069 | 0.0702 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0177 | 0.2563 | 0.4044 |
Loa Loa (eye worm) | hypothetical protein | 0.0069 | 0.0702 | 0.104 |
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.