Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | jmjC domain containing protein | 0.0202 | 0.0263 | 0.0263 |
Toxoplasma gondii | PHD-finger domain-containing protein | 0.0062 | 0 | 0.5 |
Echinococcus granulosus | Transcription factor JmjC domain containing protein | 0.0202 | 0.0263 | 0.0263 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0075 | 0.0024 | 0.0024 |
Echinococcus multilocularis | jumonji domain containing protein | 0.0086 | 0.0045 | 0.0045 |
Giardia lamblia | PHD finger protein 15 | 0.0062 | 0 | 0.5 |
Loa Loa (eye worm) | indoleamine 2,3-dioxygenase | 0.5405 | 1 | 1 |
Plasmodium falciparum | phd finger protein, putative | 0.0062 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.5405 | 1 | 1 |
Echinococcus granulosus | jumonji domain containing protein | 0.0086 | 0.0045 | 0.0045 |
Schistosoma mansoni | jumonji domain containing protein | 0.0161 | 0.0185 | 0.0185 |
Brugia malayi | jmjC domain containing protein | 0.0075 | 0.0024 | 0.0024 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0127 | 0.0123 | 0.0123 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0075 | 0.0024 | 0.0024 |
Echinococcus granulosus | lysine specific demethylase 5A | 0.0075 | 0.0024 | 0.0024 |
Plasmodium vivax | hypothetical protein, conserved | 0.0062 | 0 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.5405 | 1 | 1 |
Echinococcus multilocularis | Transcription factor, JmjC domain containing protein | 0.0202 | 0.0263 | 0.0263 |
Toxoplasma gondii | PHD-finger domain-containing protein | 0.0062 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0106 | 0.0083 | 0.0083 |
Onchocerca volvulus | Alhambra homolog | 0.0062 | 0 | 0.5 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0075 | 0.0024 | 0.0024 |
Echinococcus multilocularis | indoleamine 2,3 dioxygenase 2 | 0.5405 | 1 | 1 |
Echinococcus granulosus | indoleamine 23 dioxygenase 2 | 0.5405 | 1 | 1 |
Echinococcus multilocularis | lysine specific demethylase 5A | 0.0075 | 0.0024 | 0.0024 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Potency (functional) | 35.4813 uM | PubChem BioAssay. qHTS of alpha-syn Inhibitors. (Class of assay: confirmatory) | ChEMBL. | No reference |
Potency (functional) | 35.4813 uM | PubChem BioAssay. qHTS of TDP-43 Inhibitors. (Class of assay: confirmatory) | ChEMBL. | No reference |
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.