Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Giardia lamblia | Hypothetical protein | 0.352 | 0.2852 | 0.5 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.5965 | 1 | 1 |
Mycobacterium ulcerans | hypothetical protein | 0.352 | 0.2852 | 0.5 |
Mycobacterium ulcerans | fructose-2,6-bisphosphatase GpmB | 0.352 | 0.2852 | 0.5 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase 1 | 0.5864 | 0.9706 | 0.9706 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.5965 | 1 | 1 |
Wolbachia endosymbiont of Brugia malayi | Na+/H+-dicarboxylate symporter | 0.3409 | 0.2525 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.5864 | 0.9706 | 0.9606 |
Mycobacterium tuberculosis | Probable C4-dicarboxylate-transport transmembrane protein DctA | 0.3409 | 0.2525 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.5965 | 1 | 1 |
Schistosoma mansoni | 6-phosphofructokinase | 0.5965 | 1 | 1 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase 1 | 0.5864 | 0.9706 | 0.9706 |
Trypanosoma brucei | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.5965 | 1 | 1 |
Chlamydia trachomatis | glutamate symporter | 0.3409 | 0.2525 | 0.5 |
Leishmania major | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.5864 | 0.9706 | 0.9706 |
Loa Loa (eye worm) | hypothetical protein | 0.342 | 0.2557 | 0.0043 |
Brugia malayi | Excitatory amino acid transporter | 0.3409 | 0.2525 | 0.5 |
Trypanosoma brucei | 6-phosphofructo-2-kinase 2 | 0.5864 | 0.9706 | 0.9706 |
Onchocerca volvulus | 0.5965 | 1 | 1 | |
Echinococcus multilocularis | 6 phosphofructo 2 kinase:fructose 2 | 0.5965 | 1 | 1 |
Entamoeba histolytica | phosphoglycerate mutase family protein, putative | 0.352 | 0.2852 | 0.5 |
Giardia lamblia | Hypothetical protein | 0.352 | 0.2852 | 0.5 |
Leishmania major | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.5965 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
CC50 (ADMET) | > 250 uM | Cytotoxicity against human MT4 cells by MTT assay | ChEMBL. | 24900718 |
IC50 (binding) | = 79 uM | Inhibition of strand transfer activity of HIV1 integrase using pre-cleaved oligonucleotide as substrate after 1 hr by ELISA | ChEMBL. | 24900718 |
IC50 (binding) | = 199 uM | Inhibition of HIV1 integrase overall inhibition using 5'-digoxigenin-labeled 5'-GACCCTTTTAGTCAGTGTGGAAAATCTCTAGCAGT-3' as substrate after 1 hr by ELISA | ChEMBL. | 24900718 |
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.