Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | adhesion regulating molecule region protein, putative | 0.01 | 1 | 0.5 |
Schistosoma mansoni | adhesion regulating molecule 1 (110 kD cell membrane glycoprotein) | 0.01 | 1 | 0.5 |
Onchocerca volvulus | Proteasomal ubiquitin receptor ADRM1 homolog | 0.0064 | 0.238 | 0.5 |
Echinococcus multilocularis | adhesion regulating molecule 1 | 0.01 | 1 | 0.5 |
Plasmodium falciparum | 26S proteasome regulatory subunit RPN13, putative | 0.0052 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.01 | 1 | 0.5 |
Leishmania major | hypothetical protein, conserved | 0.0052 | 0 | 0.5 |
Echinococcus granulosus | adhesion regulating molecule 1 | 0.01 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 25.63 % | Inhibition of chymotrypsin-like enzyme activity of purified human 20S proteasome using Suc-Leu-Leu-Val-Tyr-AMC as substrate at 1 ug/ml by fluorescence method | ChEMBL. | 24767818 |
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.