Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | aldo keto reductase | 0.0317 | 1 | 1 |
Loa Loa (eye worm) | oxidoreductase | 0.0317 | 1 | 1 |
Onchocerca volvulus | 0.0092 | 0.1647 | 0.1647 | |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Leishmania major | aldo-keto reductase-like protein | 0.0317 | 1 | 1 |
Mycobacterium tuberculosis | Probable oxidoreductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Leishmania major | prostaglandin f2-alpha synthase/D-arabinose dehydrogenase | 0.0317 | 1 | 1 |
Trypanosoma cruzi | aldo/keto reductase, putative | 0.0317 | 1 | 1 |
Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.0317 | 1 | 1 |
Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Loa Loa (eye worm) | oxidoreductase | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Mycobacterium leprae | Conserved hypothetical protein | 0.0225 | 0.6594 | 0.5922 |
Loa Loa (eye worm) | oxidoreductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldehyde reductase | 0.0225 | 0.6594 | 0.6594 |
Echinococcus multilocularis | aldo keto reductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Plasmodium vivax | oxidoreductase, aldo/keto reductase domain containing protein | 0.0092 | 0.1647 | 0.5 |
Mycobacterium leprae | PROBABLE OXIDOREDUCTASE | 0.0317 | 1 | 1 |
Schistosoma mansoni | potassium channel beta | 0.0092 | 0.1647 | 0.1647 |
Trypanosoma cruzi | aldo-keto reductase | 0.0317 | 1 | 1 |
Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.0317 | 1 | 1 |
Giardia lamblia | Aldose reductase | 0.0317 | 1 | 0.5 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Loa Loa (eye worm) | oxidoreductase | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase | 0.0317 | 1 | 1 |
Giardia lamblia | Aldose reductase | 0.0317 | 1 | 0.5 |
Echinococcus granulosus | hypothetical protein | 0.0317 | 1 | 1 |
Entamoeba histolytica | aldose reductase, putative | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo/keto reductase, putative | 0.0317 | 1 | 1 |
Entamoeba histolytica | aldose reductase, putative | 0.0317 | 1 | 1 |
Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Entamoeba histolytica | aldose reductase, putative | 0.0317 | 1 | 1 |
Schistosoma mansoni | pol-related | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo/keto reductase, putative | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldehyde reductase | 0.0225 | 0.6594 | 0.6594 |
Loa Loa (eye worm) | oxidoreductase | 0.0317 | 1 | 1 |
Mycobacterium ulcerans | oxidoreductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Brugia malayi | NADH-dependent xylose reductase | 0.0092 | 0.1647 | 0.1647 |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Toxoplasma gondii | aldose reductase, putative | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Loa Loa (eye worm) | glutamate-cysteine ligase modifier subunit | 0.0092 | 0.1647 | 0.1647 |
Plasmodium vivax | aldehyde reductase, putative | 0.0092 | 0.1647 | 0.5 |
Schistosoma mansoni | aldo-keto reductase | 0.0317 | 1 | 1 |
Plasmodium falciparum | aldehyde reductase, putative | 0.0092 | 0.1647 | 0.5 |
Echinococcus granulosus | voltage gated potassium channel subunit | 0.0092 | 0.1647 | 0.1647 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0317 | 1 | 1 |
Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.0317 | 1 | 1 |
Plasmodium falciparum | aldo-keto reductase, putative | 0.0092 | 0.1647 | 0.5 |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Leishmania major | aldehyde reductase, putative,oxidoreductase, putative | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Trypanosoma brucei | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Schistosoma mansoni | aldo-keto reductase | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.0317 | 1 | 1 |
Echinococcus multilocularis | aldo keto reductase | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Trypanosoma brucei | prostaglandin f synthase | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo/keto reductase, putative | 0.0317 | 1 | 1 |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Leishmania major | prostaglandin f synthase, putative | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Brugia malayi | glutamate-cysteine ligase modifier subunit | 0.0092 | 0.1647 | 0.1647 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Echinococcus multilocularis | voltage gated potassium channel subunit | 0.0092 | 0.1647 | 0.1647 |
Onchocerca volvulus | 0.0317 | 1 | 1 | |
Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Trichomonas vaginalis | aldo-keto reductase, putative | 0.0317 | 1 | 1 |
Echinococcus granulosus | aldo keto reductase family 1, member B4 | 0.0092 | 0.1647 | 0.1647 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (functional) | = 0 % | GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 LDH activity, using an LDH reporter assay. Test compounds present at 2uM | ChEMBL. | 20485427 |
Inhibition (functional) | = 0.81 % | ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGLUT1 that are glucose transport deficient and complemented with the human glucose transporter GLUT1. Activity is measured by DNA content using SYBR green in vitro | ChEMBL. | No reference |
Inhibition (functional) | = 2.67 % | ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmPfHT that are glucose transport deficient and complemented with the Plasmodium falciparum hexose transporter. Activity is measured by by DNA content using SYBR green in vitro | ChEMBL. | No reference |
Inhibition (functional) | = 3.22 % | ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGT2 that are glucose transport deficient and complemented with the L. Mexicana glucose transporter 2. Activity is measured by by DNA content using SYBR green in vitro | ChEMBL. | No reference |
Inhibition (functional) | = 43 % | GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. | ChEMBL. | 20485427 |
Inhibition (functional) | = 92 % | GSK_TCMDC: Inhibition of Plasmodium falciparum Dd2 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM | ChEMBL. | 20485427 |
Inhibition (functional) | = 100 % | GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM | ChEMBL. | 20485427 |
Inhibition frequency index (IFI) (functional) | = 8.33 | Inhibition Frequency Index (IFI) | GSK. | 20485427 |
Percent growth inhibition (functional) | = -6 % | Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 43 % | Percent inhibition of HepG2 growth (at 10 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 92 % | Percent inhibition of P. falciparum Dd2 growth (at 2 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 101 % | Percent inhibition of P. falciparum 3D7 growth (at 2 uM) | GSK. | 20485427 |
XC50 (functional) | = 6.1 | XC50 determination of P. falciparum 3D7 growth | GSK. | 20485427 |
XC50 (functional) | = 0.79939 uM | GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole erythrocytes, using parasite LDH activity as an index of growth. | ChEMBL. | 20485427 |
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.
1 literature reference was collected for this gene.