Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | Dipeptidyl-peptidase 8-like, putative | 0.1544 | 0.9002 | 1 |
Toxoplasma gondii | dipeptidyl peptidase iv (dpp iv) n-terminal region domain-containing protein | 0.0971 | 0.4664 | 1 |
Echinococcus granulosus | dipeptidyl aminopeptidaseprotein | 0.1676 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0732 | 0.2855 | 0.2855 |
Brugia malayi | prolyl oligopeptidase family protein | 0.1544 | 0.9002 | 0.9002 |
Echinococcus multilocularis | Lysosomal Pro X carboxypeptidase | 0.0371 | 0.0128 | 0.0128 |
Schistosoma mansoni | family S28 unassigned peptidase (S28 family) | 0.0371 | 0.0128 | 0.0128 |
Echinococcus granulosus | Dipeptidyl peptidase 9 | 0.1544 | 0.9002 | 0.9002 |
Loa Loa (eye worm) | hypothetical protein | 0.0813 | 0.3467 | 0.3467 |
Trypanosoma cruzi | serine peptidase, Clan SC, Family S9B | 0.1544 | 0.9002 | 1 |
Brugia malayi | hypothetical protein | 0.0732 | 0.2855 | 0.2855 |
Trypanosoma brucei | serine peptidase, Clan SC, Family S9B | 0.1544 | 0.9002 | 1 |
Schistosoma mansoni | dipeptidyl-peptidase 9 (S09 family) | 0.1544 | 0.9002 | 0.9002 |
Loa Loa (eye worm) | prolyl oligopeptidase | 0.1676 | 1 | 1 |
Onchocerca volvulus | Dipeptidyl peptidase family member 1 homolog | 0.1676 | 1 | 1 |
Echinococcus granulosus | Lysosomal Pro X carboxypeptidase | 0.0371 | 0.0128 | 0.0128 |
Leishmania major | dipeptidyl-peptidase 8-like serine peptidase, putative,serine peptidase, Clan SC, Family S9B | 0.1544 | 0.9002 | 1 |
Echinococcus multilocularis | dipeptidyl aminopeptidaseprotein | 0.1676 | 1 | 1 |
Trypanosoma cruzi | dipeptidyl-peptidase 8-like serine peptidase | 0.1544 | 0.9002 | 1 |
Echinococcus multilocularis | Dipeptidyl peptidase 9 | 0.1544 | 0.9002 | 0.9002 |
Schistosoma mansoni | subfamily S9B unassigned peptidase (S09 family) | 0.1676 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
S | = 0.047 mg ml-1 | Solubility | ChEMBL. | 12873502 |
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.