Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | macrophage migration inhibitory factor (glycosylation-inhibiting factor) | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | Tolloid protein 1 | 0.014 | 0 | 0.5 |
Plasmodium falciparum | macrophage migration inhibitory factor | 0.0205 | 1 | 0.5 |
Entamoeba histolytica | macrophage migration inhibitory factor-like protein | 0.0205 | 1 | 0.5 |
Toxoplasma gondii | macrophage migration inhibitory factor, putative | 0.0205 | 1 | 1 |
Schistosoma mansoni | subfamily M12A unassigned peptidase (M12 family) | 0.014 | 0 | 0.5 |
Loa Loa (eye worm) | macrophage migration inhibitory factor | 0.0205 | 1 | 1 |
Leishmania major | macrophage migration inhibitory factor-like protein | 0.0205 | 1 | 0.5 |
Echinococcus multilocularis | fibrillin 1 | 0.014 | 0 | 0.5 |
Echinococcus granulosus | laminin | 0.014 | 0 | 0.5 |
Schistosoma mansoni | egf-like domain protein | 0.014 | 0 | 0.5 |
Leishmania major | macrophage migration inhibitory factor-like protein | 0.0205 | 1 | 0.5 |
Echinococcus multilocularis | Tolloid protein 1 | 0.014 | 0 | 0.5 |
Giardia lamblia | Macrophage migration inhibitory factor | 0.0205 | 1 | 0.5 |
Trichomonas vaginalis | macrophage migration inhibitory factor, mif, putative | 0.0205 | 1 | 0.5 |
Echinococcus multilocularis | laminin | 0.014 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0205 | 1 | 0.5 |
Plasmodium vivax | macrophage migration inhibitory factor, putative | 0.0205 | 1 | 0.5 |
Onchocerca volvulus | Arrow homolog | 0.014 | 0 | 0.5 |
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.