Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Pneumocystis carinii | Dihydrofolate reductase | Starlite/ChEMBL | References |
Toxoplasma gondii | bifunctional dihydrofolate reductase-thymidylate synthase | Starlite/ChEMBL | References |
Rattus norvegicus | Dihydrofolate reductase | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | DEAH box polypeptide 35 | 0.0168 | 0.0953 | 0.0953 |
Chlamydia trachomatis | dihydrofolate reductase | 0.0468 | 0.596 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0323 | 0.3542 | 0.5723 |
Giardia lamblia | Rrm3p helicase | 0.0323 | 0.3542 | 0.5 |
Mycobacterium tuberculosis | Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) | 0.0468 | 0.596 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0162 | 0.0837 | 0.0837 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0323 | 0.3542 | 0.5 |
Brugia malayi | thymidylate synthase | 0.013 | 0.0306 | 0.0306 |
Schistosoma mansoni | dihydrofolate reductase | 0.0468 | 0.596 | 1 |
Schistosoma mansoni | subfamily M12A unassigned peptidase (M12 family) | 0.0162 | 0.0837 | 0.0939 |
Brugia malayi | Probable ATP-dependent helicase DHX35 | 0.0168 | 0.0953 | 0.0953 |
Onchocerca volvulus | 0.0135 | 0.0386 | 0.1505 | |
Brugia malayi | Dihydrofolate reductase | 0.0468 | 0.596 | 0.596 |
Toxoplasma gondii | bifunctional dihydrofolate reductase-thymidylate synthase | 0.0341 | 0.3843 | 1 |
Plasmodium falciparum | bifunctional dihydrofolate reductase-thymidylate synthase | 0.0341 | 0.3843 | 0.5 |
Onchocerca volvulus | Arrow homolog | 0.0162 | 0.0837 | 1 |
Brugia malayi | Calcium binding EGF domain containing protein | 0.0162 | 0.0837 | 0.0837 |
Brugia malayi | Low-density lipoprotein receptor repeat class B containing protein | 0.0162 | 0.0837 | 0.0837 |
Loa Loa (eye worm) | multiple epidermal growth factor-like domains 6 | 0.0162 | 0.0837 | 0.0837 |
Echinococcus granulosus | dihydrofolate reductase | 0.0468 | 0.596 | 0.8676 |
Echinococcus multilocularis | laminin | 0.0162 | 0.0837 | 0.0815 |
Plasmodium vivax | bifunctional dihydrofolate reductase-thymidylate synthase, putative | 0.0341 | 0.3843 | 0.5 |
Loa Loa (eye worm) | low-density lipoprotein receptor repeat class B containing protein | 0.0162 | 0.0837 | 0.0837 |
Echinococcus multilocularis | fibrillin 1 | 0.0162 | 0.0837 | 0.0815 |
Echinococcus granulosus | laminin | 0.0162 | 0.0837 | 0.0815 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0135 | 0.0386 | 0.0141 |
Echinococcus granulosus | ATP dependent DNA helicase PIF1 | 0.0323 | 0.3542 | 0.4965 |
Loa Loa (eye worm) | integrin beta-2 | 0.071 | 1 | 1 |
Echinococcus multilocularis | Tolloid protein 1 | 0.0162 | 0.0837 | 0.0815 |
Brugia malayi | Fibulin-1 precursor | 0.0162 | 0.0837 | 0.0837 |
Trypanosoma brucei | dihydrofolate reductase-thymidylate synthase | 0.0341 | 0.3843 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0162 | 0.0837 | 0.0837 |
Loa Loa (eye worm) | bone morphogenetic protein 1b | 0.0162 | 0.0837 | 0.0837 |
Loa Loa (eye worm) | hypothetical protein | 0.0135 | 0.0386 | 0.0386 |
Brugia malayi | dihydrofolate reductase family protein | 0.0468 | 0.596 | 0.596 |
Loa Loa (eye worm) | hypothetical protein | 0.0162 | 0.0837 | 0.0837 |
Trypanosoma cruzi | dihydrofolate reductase-thymidylate synthase | 0.0341 | 0.3843 | 1 |
Mycobacterium leprae | DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) | 0.0468 | 0.596 | 1 |
Entamoeba histolytica | DNA repair and recombination protein, putative | 0.0323 | 0.3542 | 0.5 |
Echinococcus granulosus | integrin beta 2 | 0.052 | 0.6823 | 1 |
Brugia malayi | Trypsin family protein | 0.0135 | 0.0386 | 0.0386 |
Echinococcus granulosus | Tolloid protein 1 | 0.0162 | 0.0837 | 0.0815 |
Schistosoma mansoni | integrin beta subunit | 0.0408 | 0.496 | 0.8232 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.0135 | 0.0386 | 0.0141 |
Loa Loa (eye worm) | dihydrofolate reductase | 0.0468 | 0.596 | 0.596 |
Loa Loa (eye worm) | hypothetical protein | 0.0168 | 0.0953 | 0.0953 |
Echinococcus multilocularis | ATP dependent DNA helicase PIF1 | 0.0323 | 0.3542 | 0.4965 |
Loa Loa (eye worm) | hypothetical protein | 0.0162 | 0.0837 | 0.0837 |
Entamoeba histolytica | hypothetical protein, conserved | 0.0323 | 0.3542 | 0.5 |
Leishmania major | dihydrofolate reductase-thymidylate synthase | 0.0341 | 0.3843 | 1 |
Echinococcus multilocularis | integrin beta 2 | 0.052 | 0.6823 | 1 |
Loa Loa (eye worm) | thymidylate synthase | 0.013 | 0.0306 | 0.0306 |
Echinococcus multilocularis | dihydrofolate reductase | 0.0468 | 0.596 | 0.8676 |
Loa Loa (eye worm) | hypothetical protein | 0.0135 | 0.0386 | 0.0386 |
Mycobacterium ulcerans | dihydrofolate reductase DfrA | 0.0468 | 0.596 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0162 | 0.0837 | 0.0837 |
Schistosoma mansoni | egf-like domain protein | 0.0162 | 0.0837 | 0.0939 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 78 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from Toxoplasma gondii. | ChEMBL. | 7658454 |
IC50 (binding) | = 78 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from Toxoplasma gondii. | ChEMBL. | 7658454 |
IC50 (binding) | = 128 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from rat | ChEMBL. | 7658454 |
IC50 (binding) | = 128 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from rat | ChEMBL. | 7658454 |
IC50 (binding) | = 940 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from Pneumocystis carinii. | ChEMBL. | 7658454 |
IC50 (binding) | = 940 nM | Inhibitory activity against purified DHFR (Dihydrofolate reductase) from Pneumocystis carinii. | ChEMBL. | 7658454 |
Selectivity (binding) | = 0.14 | Ratio of IC50 evaluated towards DHFR of rat liver to P. cainii | ChEMBL. | 7658454 |
Selectivity (binding) | = 1.64 | Ratio of IC50 evaluated towards DHFR of rat liver to T. gondii | ChEMBL. | 7658454 |
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.