Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | coagulation factor II (thrombin) | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | RNA recognition domain-containing protein domain-containing protein | 0.0133 | 0.3684 | 0.3684 |
Schistosoma mansoni | hypothetical protein | 0.0173 | 0.5281 | 0.5281 |
Schistosoma mansoni | hypothetical protein | 0.0043 | 0.0172 | 0.0172 |
Brugia malayi | hypothetical protein | 0.0039 | 0.0006 | 0.0006 |
Echinococcus multilocularis | expressed protein | 0.0051 | 0.0477 | 0.0343 |
Brugia malayi | TAR-binding protein | 0.0133 | 0.3684 | 0.3684 |
Trichomonas vaginalis | glutaminase, putative | 0.0293 | 1 | 0.5 |
Leishmania major | hypothetical protein, conserved | 0.0098 | 0.2309 | 0.5 |
Loa Loa (eye worm) | pigment dispersing factor receptor c | 0.0057 | 0.0712 | 0.0712 |
Schistosoma mansoni | tar DNA-binding protein | 0.0133 | 0.3684 | 0.3684 |
Echinococcus multilocularis | geminin | 0.0173 | 0.5281 | 0.5751 |
Brugia malayi | RNA binding protein | 0.0133 | 0.3684 | 0.3684 |
Loa Loa (eye worm) | glutaminase | 0.0293 | 1 | 1 |
Mycobacterium ulcerans | glutaminase | 0.0293 | 1 | 0.5 |
Brugia malayi | Mitochondrial import inner membrane translocase subunit Tim17 family protein | 0.0043 | 0.0172 | 0.0172 |
Toxoplasma gondii | mitochondrial import inner membrane translocase subunit TIM10, putative | 0.0051 | 0.0477 | 1 |
Echinococcus granulosus | geminin | 0.0173 | 0.5281 | 0.56 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0094 | 0.2167 | 0.5 |
Brugia malayi | Mitochondrial import inner membrane translocase subunit Tim17 family protein | 0.0043 | 0.0172 | 0.0172 |
Schistosoma mansoni | mitochondrial import inner membrane translocase subunit tim10 | 0.0051 | 0.0477 | 0.0477 |
Loa Loa (eye worm) | TAR-binding protein | 0.0133 | 0.3684 | 0.3684 |
Loa Loa (eye worm) | glutaminase 2 | 0.0293 | 1 | 1 |
Brugia malayi | hypothetical protein | 0.0039 | 0.0006 | 0.0006 |
Echinococcus multilocularis | tar DNA binding protein | 0.0133 | 0.3684 | 0.3954 |
Loa Loa (eye worm) | RNA binding protein | 0.0133 | 0.3684 | 0.3684 |
Schistosoma mansoni | tar DNA-binding protein | 0.0133 | 0.3684 | 0.3684 |
Schistosoma mansoni | tar DNA-binding protein | 0.0133 | 0.3684 | 0.3684 |
Toxoplasma gondii | TIM10 family protein, putative | 0.0051 | 0.0477 | 1 |
Schistosoma mansoni | tar DNA-binding protein | 0.0133 | 0.3684 | 0.3684 |
Schistosoma mansoni | tar DNA-binding protein | 0.0133 | 0.3684 | 0.3684 |
Plasmodium vivax | mitochondrial import inner membrane translocase subunit TIM10, putative | 0.0051 | 0.0477 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0173 | 0.5281 | 0.5281 |
Schistosoma mansoni | glutaminase | 0.0293 | 1 | 1 |
Echinococcus multilocularis | DNA dependent protein kinase catalytic subunit | 0.0269 | 0.9055 | 1 |
Brugia malayi | Calcitonin receptor-like protein seb-1 | 0.0057 | 0.0712 | 0.0712 |
Brugia malayi | Mitochondrial import inner membrane translocase subunit TIM10 | 0.0051 | 0.0477 | 0.0477 |
Brugia malayi | RNA recognition motif domain containing protein | 0.0133 | 0.3684 | 0.3684 |
Plasmodium falciparum | mitochondrial import inner membrane translocase subunit TIM10, putative | 0.0051 | 0.0477 | 1 |
Loa Loa (eye worm) | transport to inner mitochondrial membrane family member | 0.0051 | 0.0477 | 0.0477 |
Brugia malayi | Corticotropin releasing factor receptor 2 precursor, putative | 0.0057 | 0.0712 | 0.0712 |
Echinococcus granulosus | tar DNA binding protein | 0.0133 | 0.3684 | 0.3739 |
Loa Loa (eye worm) | hypothetical protein | 0.0043 | 0.0172 | 0.0172 |
Echinococcus granulosus | DNA dependent protein kinase catalytic subunit | 0.0269 | 0.9055 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0057 | 0.0712 | 0.0712 |
Brugia malayi | Mitochondrial import inner membrane translocase subunit Tim17 family protein | 0.0043 | 0.0172 | 0.0172 |
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.