Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Plasmodium vivax | proteasome subunit beta type-5, putative | 0.0076 | 0.5 | 0.5 |
Mycobacterium leprae | proteasome (beta subunit) PrcB | 0.0076 | 0.5 | 0.5 |
Toxoplasma gondii | proteasome subunit beta type, putative | 0.0076 | 0.5 | 0.5 |
Plasmodium falciparum | proteasome subunit beta type-5 | 0.0076 | 0.5 | 0.5 |
Trypanosoma brucei | proteasome subunit beta type-5, putative | 0.0076 | 0.5 | 0.5 |
Giardia lamblia | Proteasome subunit beta type 5 precursor | 0.0076 | 0.5 | 0.5 |
Leishmania major | proteasome beta 5 subunit, putative | 0.0076 | 0.5 | 0.5 |
Loa Loa (eye worm) | proteasome A-type and B-type family protein | 0.0076 | 0.5 | 0.5 |
Mycobacterium tuberculosis | Proteasome beta subunit PrcB; assembles with alpha subunit PrcA. | 0.0076 | 0.5 | 0.5 |
Trichomonas vaginalis | Family T1, proteasome beta subunit, threonine peptidase | 0.0076 | 0.5 | 0.5 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0076 | 0.5 | 0.5 |
Echinococcus granulosus | proteasome prosome macropain | 0.0076 | 0.5 | 0.5 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0076 | 0.5 | 0.5 |
Echinococcus multilocularis | proteasome (prosome, macropain) | 0.0076 | 0.5 | 0.5 |
Schistosoma mansoni | proteasome catalytic subunit 3 (T01 family) | 0.0076 | 0.5 | 0.5 |
Entamoeba histolytica | proteasome subunit beta type 5 precursor, putative | 0.0076 | 0.5 | 0.5 |
Mycobacterium ulcerans | proteasome PrcB | 0.0076 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | = 20 % | In vitro percent inhibition against 5-lipoxygenase in RBL-1 cells at 10 uM concentration | ChEMBL. | 11277534 |
Inhibition (binding) | = 20 % | In vitro percent inhibition against 5-lipoxygenase in RBL-1 cells at 10 uM concentration | ChEMBL. | 11277534 |
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.