Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Entamoeba histolytica | Niemann-Pick C1 protein, putative | 0.0099 | 0.2568 | 0.5 |
Mycobacterium tuberculosis | Probable bifunctional purine biosynthesis protein PurH: phosphoribosylaminoimidazolecarboxamide formyltransferase (AICAR transfo | 0.0245 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0099 | 0.2568 | 1 |
Echinococcus granulosus | Niemann Pick C1 protein | 0.0099 | 0.2568 | 0.1238 |
Brugia malayi | Niemann-Pick C1 protein precursor | 0.0099 | 0.2568 | 0.5 |
Echinococcus multilocularis | expressed conserved protein | 0.0093 | 0.2263 | 0.4786 |
Echinococcus multilocularis | Niemann Pick C1 protein | 0.0099 | 0.2568 | 0.5432 |
Wolbachia endosymbiont of Brugia malayi | AICAR transformylase/IMP cyclohydrolase PurH | 0.0245 | 1 | 0.5 |
Schistosoma mansoni | niemann-pick C1 (NPC1) | 0.0101 | 0.2646 | 0.5 |
Echinococcus granulosus | Niemann Pick C1 protein | 0.0142 | 0.4729 | 1 |
Echinococcus multilocularis | Niemann Pick C1 protein | 0.0142 | 0.4729 | 1 |
Mycobacterium ulcerans | bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase | 0.0245 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Ki (binding) | = 0.15 uM | Inhibitory activity of compound against inosine-uridine nucleoside hydrolase (IU-NH) from crithidia fasciculata | ChEMBL. | 12502369 |
Ki (binding) | = 14 uM | Inhibitory activity of compound against perine-specific inosine-adenosine-guanosine nucleoside hydrolase (IAG-NH) from trypanosoma brucei | ChEMBL. | 12502369 |
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.