Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Putative carbonic anhydrase 5 precursor | 0.0726 | 0 | 0.5 |
Leishmania major | carbonic anhydrase family protein, putative | 0.3216 | 1 | 1 |
Mycobacterium ulcerans | carbonic anhydrase | 0.3216 | 1 | 1 |
Echinococcus granulosus | carbonic anhydrase II | 0.0726 | 0 | 0.5 |
Mycobacterium tuberculosis | Beta-carbonic anhydrase CanB | 0.1795 | 0.4294 | 1 |
Trypanosoma brucei | carbonic anhydrase-like protein | 0.0726 | 0 | 0.5 |
Trypanosoma cruzi | carbonic anhydrase-like protein, putative | 0.0726 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.109 | 0.1461 | 1 |
Trichomonas vaginalis | conserved hypothetical protein | 0.2453 | 0.6936 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.2453 | 0.6936 | 0.5 |
Trypanosoma cruzi | carbonic anhydrase-like protein, putative | 0.0726 | 0 | 0.5 |
Mycobacterium leprae | CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) | 0.3216 | 1 | 0.5 |
Echinococcus multilocularis | carbonic anhydrase II | 0.0726 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable transmembrane carbonic anhydrase (carbonate dehydratase) (carbonic dehydratase) | 0.1671 | 0.3793 | 0.8365 |
Schistosoma mansoni | carbonic anhydrase | 0.3216 | 1 | 1 |
Brugia malayi | Eukaryotic-type carbonic anhydrase family protein | 0.0726 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
NOHA (functional) | = 5 % | Nitric oxide (NO) formation during oxidation of NADPH and O2, catalyzed by NOS II detected spectrophotometrically using hemoglobin assay. | ChEMBL. | 11831907 |
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.