Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | proteasome (prosome, macropain) subunit, beta type, 5 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Plasmodium falciparum | proteasome subunit alpha type-5, putative | proteasome (prosome, macropain) subunit, beta type, 5 | 160 aa | 148 aa | 23.0 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.005 | 0.312 | 0.312 |
Echinococcus granulosus | jumonji domain containing protein | 0.0041 | 0.1721 | 0.1721 |
Echinococcus multilocularis | proteasome (prosome, macropain) | 0.0086 | 0.8503 | 0.8503 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0061 | 0.468 | 0.5504 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.314 | 0.3693 |
Schistosoma mansoni | proteasome catalytic subunit 3 (T01 family) | 0.0086 | 0.8503 | 1 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0036 | 0.0925 | 0.1088 |
Echinococcus multilocularis | lysine specific demethylase 5A | 0.0036 | 0.0925 | 0.0925 |
Giardia lamblia | Proteasome subunit beta type 5 precursor | 0.0086 | 0.8503 | 1 |
Loa Loa (eye worm) | jmjC domain-containing protein | 0.0036 | 0.0925 | 0.1088 |
Plasmodium vivax | proteasome subunit beta type-5, putative | 0.0086 | 0.8503 | 1 |
Entamoeba histolytica | proteasome subunit beta type 5 precursor, putative | 0.0086 | 0.8503 | 0.5 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0086 | 0.8503 | 0.5 |
Trichomonas vaginalis | Family T1, proteasome beta subunit, threonine peptidase | 0.0086 | 0.8503 | 0.5 |
Brugia malayi | latrophilin 2 splice variant baaae | 0.0034 | 0.0742 | 0.0742 |
Echinococcus granulosus | lysine specific demethylase 5A | 0.0036 | 0.0925 | 0.0925 |
Onchocerca volvulus | Alhambra homolog | 0.0029 | 0 | 0.5 |
Toxoplasma gondii | proteasome subunit beta type, putative | 0.0086 | 0.8503 | 1 |
Schistosoma mansoni | jumonji domain containing protein | 0.0076 | 0.7041 | 0.8281 |
Echinococcus granulosus | Transcription factor JmjC domain containing protein | 0.0096 | 1 | 1 |
Schistosoma mansoni | jumonji/arid domain-containing protein | 0.0036 | 0.0925 | 0.1088 |
Leishmania major | proteasome beta 5 subunit, putative | 0.0086 | 0.8503 | 0.5 |
Echinococcus granulosus | proteasome prosome macropain | 0.0086 | 0.8503 | 0.8503 |
Trypanosoma brucei | proteasome subunit beta type-5, putative | 0.0086 | 0.8503 | 0.5 |
Brugia malayi | jmjC domain containing protein | 0.0036 | 0.0925 | 0.0925 |
Loa Loa (eye worm) | proteasome A-type and B-type family protein | 0.0086 | 0.8503 | 1 |
Plasmodium falciparum | proteasome subunit beta type-5 | 0.0086 | 0.8503 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.005 | 0.312 | 0.367 |
Brugia malayi | Proteasome A-type and B-type family protein | 0.0086 | 0.8503 | 0.8503 |
Echinococcus multilocularis | jumonji domain containing protein | 0.0041 | 0.1721 | 0.1721 |
Mycobacterium ulcerans | proteasome PrcB | 0.0086 | 0.8503 | 0.5 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.005 | 0.312 | 0.312 |
Trypanosoma cruzi | proteasome subunit beta type-5, putative | 0.0086 | 0.8503 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0034 | 0.0742 | 0.0873 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.005 | 0.312 | 0.367 |
Mycobacterium tuberculosis | Proteasome beta subunit PrcB; assembles with alpha subunit PrcA. | 0.0086 | 0.8503 | 0.5 |
Echinococcus multilocularis | Transcription factor, JmjC domain containing protein | 0.0096 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0034 | 0.0742 | 0.0873 |
Mycobacterium leprae | proteasome (beta subunit) PrcB | 0.0086 | 0.8503 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
EC50 (binding) | = 332 nM | Inhibition of chymotrypsin like activity of 20S proteasome in HEK293 cells after 24 hrs by microscopic analysis | ChEMBL. | 24269479 |
IC50 (binding) | = 500 nM | Inhibition of chymotrypsin like activity of human 20S proteasome after 1 hr by luminescence assay | ChEMBL. | 24269479 |
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.