Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | fructose 16 bisphosphatase 1 | 0.6616 | 1 | 0.5 |
Mycobacterium tuberculosis | Halimadienyl diphosphate synthase | 0.0144 | 0 | 0.5 |
Leishmania major | 0.6616 | 1 | 1 | |
Trypanosoma cruzi | sedoheptulose-1,7-bisphosphatase, putative | 0.246 | 0.3579 | 0.3506 |
Schistosoma mansoni | fructose-16-bisphosphatase-related | 0.6616 | 1 | 1 |
Trypanosoma cruzi | fructose-1,6-bisphosphatase, cytosolic, putative | 0.6616 | 1 | 1 |
Toxoplasma gondii | fructose-bisphospatase II | 0.6616 | 1 | 1 |
Trypanosoma brucei | sedoheptulose-1,7-bisphosphatase | 0.246 | 0.3579 | 0.3506 |
Loa Loa (eye worm) | fructose-1,6-bisphosphatase | 0.6616 | 1 | 0.5 |
Trypanosoma cruzi | fructose-1,6-bisphosphatase, cytosolic, putative | 0.6616 | 1 | 1 |
Trypanosoma cruzi | sedoheptulose-1,7-bisphosphatase, putative | 0.246 | 0.3579 | 0.3506 |
Trypanosoma brucei | fructose-1,6-bisphosphatase | 0.6616 | 1 | 1 |
Echinococcus multilocularis | fructose 1,6 bisphosphatase 1 | 0.6616 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | > 100 uM | Inhibitory activity against tetracycline uptake in everted membrane vesicles derived from Tc-resistant Escherichia coli bearing class B tetracycline resistance efflux protein (Tet) | ChEMBL. | 8176712 |
IC50 (functional) | > 100 uM | Inhibitory activity against tetracycline uptake in everted membrane vesicles derived from Tc-resistant Escherichia coli bearing class B tetracycline resistance efflux protein (Tet) | ChEMBL. | 8176712 |
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.