Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | mitochondrial DNA polymerase beta | 0.0299 | 0.9829 | 1 |
Echinococcus multilocularis | DNA dependent protein kinase catalytic subunit | 0.0303 | 1 | 0.5 |
Mycobacterium tuberculosis | Conserved hypothetical protein | 0.0157 | 0.4416 | 0.5 |
Trypanosoma cruzi | mitochondrial DNA polymerase beta-PAK, putative | 0.0051 | 0.0352 | 0.0358 |
Leishmania major | mitochondrial DNA polymerase beta | 0.0299 | 0.9829 | 1 |
Mycobacterium ulcerans | hypothetical protein | 0.0157 | 0.4416 | 0.5 |
Trypanosoma brucei | mitochondrial DNA polymerase beta-PAK | 0.0142 | 0.3805 | 0.3871 |
Toxoplasma gondii | hypothetical protein | 0.0048 | 0.0236 | 0.5 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0106 | 0.2452 | 0.2495 |
Trypanosoma cruzi | mitochondrial DNA polymerase beta-PAK, putative | 0.0142 | 0.3805 | 0.3871 |
Trypanosoma cruzi | mitochondrial DNA polymerase beta, putative | 0.0299 | 0.9829 | 1 |
Trypanosoma cruzi | mitochondrial DNA polymerase beta, putative | 0.0299 | 0.9829 | 1 |
Leishmania major | mitochondrial DNA polymerase beta-PAK, putative | 0.0142 | 0.3805 | 0.1658 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 25 uM | Inhibition of Staphylococcus aureus 7,8-dihydroneopterin aldolase | ChEMBL. | 15027862 |
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.