Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | mitogen-activated protein kinase 13 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Trypanosoma brucei | mitogen-activated protein kinase 5 | mitogen-activated protein kinase 13 | 365 aa | 366 aa | 30.1 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Echinococcus multilocularis | plexin a4 | 0.0446 | 1 | 1 |
Echinococcus multilocularis | semaphorin 5B | 0.0158 | 0.1954 | 0.0185 |
Echinococcus granulosus | semaphorin 5B | 0.0158 | 0.1954 | 0.0185 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0158 | 0.1954 | 0.0185 |
Trypanosoma cruzi | mitogen-activated protein kinase 3, putative | 0.0152 | 0.1802 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0219 | 0.3682 | 0.2292 |
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Echinococcus granulosus | semaphorin 1A | 0.0158 | 0.1954 | 0.0185 |
Echinococcus granulosus | plexin a4 | 0.0446 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0377 | 0.8075 | 0.7652 |
Brugia malayi | Sema domain containing protein | 0.0158 | 0.1954 | 0.0185 |
Schistosoma mansoni | plexin | 0.0219 | 0.3682 | 0.2822 |
Echinococcus multilocularis | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Loa Loa (eye worm) | plexin A | 0.0446 | 1 | 1 |
Brugia malayi | Sema domain containing protein | 0.0158 | 0.1954 | 0.0185 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0158 | 0.1954 | 0.0185 |
Brugia malayi | Plexin repeat family protein | 0.0377 | 0.8075 | 0.7652 |
Entamoeba histolytica | protein kinase domain containing protein | 0.0087 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Schistosoma mansoni | plexin | 0.0377 | 0.8075 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Leishmania major | mitogen-activated protein kinase 3, putative,map kinase 3, putative | 0.0152 | 0.1802 | 0.5 |
Onchocerca volvulus | 0.0377 | 0.8075 | 1 | |
Loa Loa (eye worm) | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Entamoeba histolytica | tyrosin kinase, putative | 0.0087 | 0 | 0.5 |
Brugia malayi | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Brugia malayi | hypothetical protein | 0.0158 | 0.1954 | 0.0185 |
Trypanosoma brucei | mitogen-activated protein kinase 3, putative | 0.0152 | 0.1802 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0219 | 0.3682 | 0.2822 |
Trypanosoma cruzi | mitogen-activated protein kinase 3, putative | 0.0152 | 0.1802 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | > 17 uM | Compound was tested for inhibition of p38 MAP kinase | ChEMBL. | 9873686 |
IC50 (binding) | > 17 uM | Compound was tested for inhibition of p38 MAP kinase | ChEMBL. | 9873686 |
IC50 (binding) | = 25 uM | In vitro inhibitory concentration against radioligand [3H]-SB-202,190 binding to CSBP kinase in human monocytic cell line, THP-1 | ChEMBL. | 8831759 |
IC50 (binding) | = 25 uM | In vitro inhibitory concentration against radioligand [3H]-SB-202,190 binding to CSBP kinase in human monocytic cell line, THP-1 | ChEMBL. | 8831759 |
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.
2 literature references were collected for this gene.