Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium tuberculosis | Probable glutamine synthetase GlnA3 (glutamine synthase) (GS-I) | 0.0677796 | 0.23692 | 0.466911 |
Echinococcus granulosus | hypothetical protein | 0.13831 | 1 | 1 |
Echinococcus multilocularis | conserved hypothetical protein | 0.137363 | 0.989762 | 1 |
Trypanosoma cruzi | glutamine synthetase, putative | 0.0468997 | 0.0110157 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | glutamine synthetase | 0.0677796 | 0.23692 | 0.5 |
Toxoplasma gondii | glutamine synthetase, type I, putative | 0.0927813 | 0.507419 | 0.5 |
Trypanosoma cruzi | glutamine synthetase, putative | 0.0468997 | 0.0110157 | 0.5 |
Loa Loa (eye worm) | Gln-2 protein | 0.0468997 | 0.0110157 | 0.5 |
Schistosoma mansoni | glutamine synthetase bacteria | 0.0677796 | 0.23692 | 1 |
Mycobacterium tuberculosis | Probable glutamine synthetase GlnA2 (glutamine synthase) (GS-II) | 0.0927813 | 0.507419 | 1 |
Plasmodium vivax | glutamine synthetase, putative | 0.0927813 | 0.507419 | 0.5 |
Leishmania major | glutamine synthetase, putative | 0.0468997 | 0.0110157 | 0.5 |
Mycobacterium ulcerans | glutamine synthetase GlnA1 | 0.0927813 | 0.507419 | 1 |
Trypanosoma brucei | glutamine synthetase, putative | 0.0468997 | 0.0110157 | 0.5 |
Mycobacterium ulcerans | glutamine synthetase | 0.0927813 | 0.507419 | 1 |
Mycobacterium leprae | PROBABLE GLUTAMINE SYNTHETASE GLNA2 (GLUTAMINE SYNTHASE) (GS-II) | 0.0927813 | 0.507419 | 1 |
Brugia malayi | Serotonin receptor | 0.0925218 | 0.504612 | 0.5 |
Onchocerca volvulus | Glutamine synthetase homolog | 0.0468997 | 0.0110157 | 0.5 |
Schistosoma mansoni | glutamine synthetase bacteria | 0.0677796 | 0.23692 | 1 |
Plasmodium falciparum | glutamine synthetase, putative | 0.0927813 | 0.507419 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 0.17 uM | Antileishmanial activity against Leishmania braziliensis MHOM/IT/2006/ISS2848 promastigotes assessed as inhibition of parasite growth after 72 hrs by MTT assay | ChEMBL. | 25497962 |
IC50 (functional) | = 0.21 uM | Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D10 assessed as inhibition of parasite growth after 72 hrs by parasite lactate dehydrogenase assay | ChEMBL. | 25497962 |
IC50 (functional) | = 0.37 uM | Antileishmanial activity against Leishmania infantum MHOM/TN/80/IPT1 promastigotes assessed as inhibition of parasite growth after 72 hrs by MTT assay | ChEMBL. | 25497962 |
Ratio IC50 (functional) | = 1.3 | Resistance index, ratio of IC50 for chloroquine-resistant Plasmodium falciparum W2 to IC50 for chloroquine-sensitive Plasmodium falciparum D10 | ChEMBL. | 25497962 |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Leishmania braziliensis | ChEMBL23 | 25497962 | |
Leishmania infantum | ChEMBL23 | 25497962 | |
Plasmodium falciparum | ChEMBL23 | 25497962 |
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.