Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | hypothetical protein | 0.0166 | 0.1839 | 1 |
Echinococcus granulosus | geminin | 0.0166 | 0.1839 | 1 |
Schistosoma mansoni | thyroid hormone receptor | 0.0161 | 0.177 | 0.8073 |
Loa Loa (eye worm) | hypothetical protein | 0.0273 | 0.3225 | 0.995 |
Toxoplasma gondii | LsmAD domain-containing protein | 0.0024 | 0 | 0.5 |
Trypanosoma brucei | PAB1-binding protein , putative | 0.0024 | 0 | 0.5 |
Onchocerca volvulus | Glucosylceramidase homolog | 0.0166 | 0.1839 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0166 | 0.1839 | 1 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.0285 | 0.3378 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0175 | 0.1955 | 0.1027 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.0274 | 0.3242 | 0.9597 |
Trypanosoma cruzi | PAB1-binding protein , putative | 0.0024 | 0 | 0.5 |
Brugia malayi | Nuclear hormone receptor-like 1 | 0.0274 | 0.3242 | 0.9597 |
Schistosoma mansoni | thyroid hormone receptor | 0.0161 | 0.177 | 0.8073 |
Echinococcus multilocularis | geminin | 0.0166 | 0.1839 | 0.042 |
Loa Loa (eye worm) | O-glycosyl hydrolase family 30 protein | 0.0253 | 0.2969 | 0.9159 |
Plasmodium falciparum | ataxin-2 like protein, putative | 0.0024 | 0 | 0.5 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0175 | 0.1955 | 0.1027 |
Leishmania major | hypothetical protein, conserved | 0.0024 | 0 | 0.5 |
Plasmodium falciparum | ataxin-2 like protein, putative | 0.0024 | 0 | 0.5 |
Plasmodium vivax | ataxin-2 like protein, putative | 0.0024 | 0 | 0.5 |
Brugia malayi | O-Glycosyl hydrolase family 30 protein | 0.0253 | 0.2969 | 0.879 |
Trypanosoma cruzi | PAB1-binding protein , putative | 0.0024 | 0 | 0.5 |
Loa Loa (eye worm) | nuclear hormone receptor-like 1 | 0.0274 | 0.3242 | 1 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
Echinococcus multilocularis | thyroid hormone receptor alpha | 0.0161 | 0.177 | 0.0339 |
Trichomonas vaginalis | glucosylceramidase, putative | 0.0253 | 0.2969 | 1 |
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) | = 11 % | 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) | = 11.88 % | 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) | = 11.96 % | 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) | = 12.06 % | 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) | = 13 % | GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. | ChEMBL. | 20485427 |
Inhibition (functional) | = 93 % | 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) | = 3.54 | Inhibition Frequency Index (IFI) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 0 % | Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 11 % | Percent inhibition of P. falciparum Dd2 growth (at 2 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 13 % | Percent inhibition of HepG2 growth (at 10 uM) | GSK. | 20485427 |
Percent growth inhibition (functional) | = 93 % | Percent inhibition of P. falciparum 3D7 growth (at 2 uM) | GSK. | 20485427 |
XC50 (functional) | = 5.79 | XC50 determination of P. falciparum 3D7 growth | GSK. | 20485427 |
XC50 (functional) | = 1.63862 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.