Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | farnesyl diphosphate synthase | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0897 |
Trypanosoma cruzi | monoglyceride lipase, putative | 0.0356 | 0.3462 | 1 |
Plasmodium falciparum | lysophospholipase, putative | 0.0356 | 0.3462 | 1 |
Giardia lamblia | Farnesyl diphosphate synthase | 0.0124 | 0.031 | 0.5 |
Trichomonas vaginalis | Clan SC, family S33, methylesterase-like serine peptidase | 0.0356 | 0.3462 | 1 |
Trypanosoma cruzi | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0897 |
Mycobacterium tuberculosis | 4,9-DHSA hydrolase | 0.082 | 0.976 | 1 |
Trichomonas vaginalis | Clan SC, family S33, methylesterase-like serine peptidase | 0.0356 | 0.3462 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0356 | 0.3462 | 1 |
Leishmania major | monoglyceride lipase, putative | 0.0356 | 0.3462 | 1 |
Plasmodium vivax | geranylgeranyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0897 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0356 | 0.3462 | 1 |
Plasmodium falciparum | lysophospholipase, putative | 0.0356 | 0.3462 | 1 |
Trichomonas vaginalis | Clan SC, family S33, methylesterase-like serine peptidase | 0.0356 | 0.3462 | 1 |
Trichomonas vaginalis | valacyclovir hydrolase, putative | 0.0356 | 0.3462 | 1 |
Echinococcus multilocularis | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.031 |
Mycobacterium ulcerans | lysophospholipase | 0.0356 | 0.3462 | 0.3483 |
Mycobacterium leprae | POSSIBLE LYSOPHOSPHOLIPASE | 0.0356 | 0.3462 | 1 |
Leishmania major | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0897 |
Loa Loa (eye worm) | polyprenyl synthetase | 0.0124 | 0.031 | 0.031 |
Trypanosoma cruzi | farnesyl pyrophosphate synthase, putative | 0.0124 | 0.031 | 0.0897 |
Trichomonas vaginalis | Clan SC, family S33, methylesterase-like serine peptidase | 0.0356 | 0.3462 | 1 |
Plasmodium falciparum | lysophospholipase, putative | 0.0356 | 0.3462 | 1 |
Schistosoma mansoni | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.031 |
Echinococcus granulosus | farnesyl pyrophosphate synthase | 0.0124 | 0.031 | 0.031 |
Toxoplasma gondii | polyprenyl synthetase superfamily protein | 0.0124 | 0.031 | 0.5 |
Mycobacterium ulcerans | 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate hydrolase BphD | 0.0833 | 0.9941 | 1 |
Mycobacterium tuberculosis | Possible lysophospholipase | 0.0356 | 0.3462 | 0.3548 |
Trypanosoma brucei | monoglyceride lipase, putative | 0.0356 | 0.3462 | 1 |
Mycobacterium ulcerans | hypothetical protein | 0.0356 | 0.3462 | 0.3483 |
Plasmodium falciparum | geranylgeranyl pyrophosphate synthase, putative | 0.0124 | 0.031 | 0.0897 |
Trypanosoma brucei | monoglyceride lipase, putative | 0.0356 | 0.3462 | 1 |
Trichomonas vaginalis | Clan SC, family S33, methylesterase-like serine peptidase | 0.0356 | 0.3462 | 1 |
Mycobacterium ulcerans | geranylgeranyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0312 |
Mycobacterium tuberculosis | Probable geranylgeranyl pyrophosphate synthetase IdsA2 (ggppsase) (GGPP synthetase) (geranylgeranyl diphosphate synthase) | 0.0124 | 0.031 | 0.0318 |
Plasmodium vivax | PST-A protein | 0.0356 | 0.3462 | 1 |
Entamoeba histolytica | hydrolase, alpha/beta fold family domain containing protein | 0.0356 | 0.3462 | 0.5 |
Brugia malayi | Polyprenyl synthetase family protein | 0.0124 | 0.031 | 0.031 |
Plasmodium falciparum | esterase, putative | 0.0356 | 0.3462 | 1 |
Entamoeba histolytica | hydrolase, alpha/beta fold family domain containing protein | 0.0356 | 0.3462 | 0.5 |
Mycobacterium ulcerans | geranylgeranyl pyrophosphate synthase | 0.0124 | 0.031 | 0.0312 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.11 uM | Inhibition of His6-tagged human truncated FPPS (6-353) expressed in Escherichia coli BL21(DE3) cells using geranyl diphosphate and isopentenyl diphosphate as substrate preincubated with enzyme for 30 mins by spectrophotometric analysis | ChEMBL. | 23610597 |
IC50 (binding) | = 0.2 uM | Binding affinity to human FPPS at 1 mM by X-ray crystallographic analysis | ChEMBL. | 23610597 |
IC50 (functional) | = 22 uM | Inhibition of Plasmodium falciparum growth after 72 hrs by LDH assay | ChEMBL. | 23610597 |
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.