Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | folylpolyglutamate synthase | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | bifunctional protein FolC subfamily protein | 0.012 | 0.2597 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0372 | 1 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0039 | 0.0195 | 0.5 |
Plasmodium falciparum | dihydrofolate synthase/folylpolyglutamate synthase | 0.012 | 0.2597 | 0.5 |
Loa Loa (eye worm) | pre-SET domain-containing protein family protein | 0.0233 | 0.5899 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0039 | 0.0195 | 0.5 |
Echinococcus granulosus | histone lysine methyltransferase setb | 0.0033 | 0.0036 | 0.0036 |
Echinococcus multilocularis | folylpolyglutamate synthase, mitochondrial | 0.012 | 0.2597 | 0.257 |
Entamoeba histolytica | hypothetical protein | 0.0039 | 0.0195 | 0.5 |
Echinococcus multilocularis | Basic leucine zipper (bZIP) transcription | 0.0039 | 0.0195 | 0.016 |
Brugia malayi | Pre-SET motif family protein | 0.0233 | 0.5899 | 1 |
Trichomonas vaginalis | set domain proteins, putative | 0.0265 | 0.6844 | 1 |
Treponema pallidum | folylpolyglutamate synthetase (folC) | 0.012 | 0.2597 | 0.5 |
Echinococcus multilocularis | folylpolyglutamate synthase, mitochondrial | 0.012 | 0.2597 | 0.257 |
Echinococcus granulosus | Basic leucine zipper bZIP transcription | 0.0039 | 0.0195 | 0.0195 |
Brugia malayi | FolC bifunctional protein | 0.012 | 0.2597 | 0.4368 |
Onchocerca volvulus | 0.0169 | 0.4024 | 0.5857 | |
Trypanosoma brucei | folylpolyglutamate synthase, putative | 0.012 | 0.2597 | 0.5 |
Plasmodium vivax | dihydrofolate synthase/folylpolyglutamate synthase, putative | 0.012 | 0.2597 | 1 |
Trypanosoma cruzi | folylpolyglutamate synthase, putative | 0.012 | 0.2597 | 0.5 |
Brugia malayi | hypothetical protein | 0.0039 | 0.0195 | 0.0271 |
Echinococcus granulosus | folylpolyglutamate synthase, mitochondrial | 0.012 | 0.2597 | 0.2597 |
Schistosoma mansoni | hypothetical protein | 0.0372 | 1 | 1 |
Onchocerca volvulus | Putative folylpolyglutamate synthase | 0.012 | 0.2597 | 0.3761 |
Mycobacterium ulcerans | folylpolyglutamate synthase protein FolC | 0.012 | 0.2597 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0039 | 0.0195 | 0.016 |
Schistosoma mansoni | folylpolyglutamate synthase | 0.012 | 0.2597 | 0.257 |
Schistosoma mansoni | transcription factor LCR-F1 | 0.0039 | 0.0195 | 0.016 |
Leishmania major | folylpolyglutamate synthetase | 0.012 | 0.2597 | 0.5 |
Loa Loa (eye worm) | FolC protein | 0.012 | 0.2597 | 0.4368 |
Echinococcus granulosus | folylpolyglutamate synthase mitochondrial | 0.012 | 0.2597 | 0.2597 |
Mycobacterium tuberculosis | Probable folylpolyglutamate synthase protein FolC (folylpoly-gamma-glutamate synthetase) (FPGS) | 0.012 | 0.2597 | 0.5 |
Brugia malayi | hypothetical protein | 0.0169 | 0.4024 | 0.6802 |
Mycobacterium leprae | PROBABLE FOLYLPOLYGLUTAMATE SYNTHASE PROTEIN FOLC (FOLYLPOLY-GAMMA-GLUTAMATE SYNTHETASE) (FPGS) | 0.012 | 0.2597 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0169 | 0.4024 | 0.6802 |
Entamoeba histolytica | hypothetical protein | 0.0039 | 0.0195 | 0.5 |
Onchocerca volvulus | 0.0265 | 0.6844 | 1 | |
Echinococcus multilocularis | geminin | 0.0372 | 1 | 1 |
Trypanosoma cruzi | folylpolyglutamate synthetase | 0.012 | 0.2597 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 0.2 uM | Binding affinity of the compound as Competitive substrate in the presence of 50 gmM aminopterin towards recombinant Human Folyl-polyglutamate synthase (FPGS) | ChEMBL. | 10479284 |
Ki (binding) | = 0.2 uM | Binding affinity of the compound as Competitive substrate in the presence of 50 gmM aminopterin towards recombinant Human Folyl-polyglutamate synthase (FPGS) | ChEMBL. | 10479284 |
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.