Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Plasmodium falciparum | dipeptidyl aminopeptidase 1 | 0.1077 | 1 | 1 |
Trichomonas vaginalis | Clan CA, family C1, cathepsin B-like cysteine peptidase | 0.0668 | 0.5757 | 0.5 |
Brugia malayi | SET domain containing protein | 0.0114 | 0 | 0.5 |
Echinococcus granulosus | histone lysine N methyltransferase Ez | 0.0114 | 0 | 0.5 |
Echinococcus multilocularis | histone lysine N methyltransferase E(z) | 0.0114 | 0 | 0.5 |
Plasmodium falciparum | dipeptidyl aminopeptidase 2 | 0.1077 | 1 | 1 |
Toxoplasma gondii | preprocathepsin c precursor, putative | 0.1077 | 1 | 1 |
Toxoplasma gondii | cathepsin CPC1 | 0.1077 | 1 | 1 |
Loa Loa (eye worm) | SET domain-containing protein | 0.0114 | 0 | 0.5 |
Schistosoma mansoni | dipeptidyl-peptidase I (C01 family) | 0.1077 | 1 | 1 |
Plasmodium vivax | dipeptidyl aminopeptidase 2, putative | 0.1077 | 1 | 1 |
Plasmodium vivax | dipeptidyl aminopeptidase 1, putative | 0.1077 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 24 uM | Inhibition of N-terminally FLAG-tagged wild type EZH2 in EZH2/SUZ12/EED/RbAp48 complex (unknown origin) expressed in baculovirus infected in SF9 cells assessed as inhibition of methylation of nucleosomes at H3K27 by scintillation counting in presence of [3H]SAM | ChEMBL. | 25746813 |
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.