Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Cavia porcellus | Platelet activating factor receptor | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Leishmania major | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.2628 | 0.9791 | 0.9706 |
Loa Loa (eye worm) | hypothetical protein | 0.1532 | 0.4715 | 0.4715 |
Trypanosoma brucei | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.2673 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.2628 | 0.9791 | 0.9791 |
Echinococcus multilocularis | 6 phosphofructo 2 kinase:fructose 2 | 0.2673 | 1 | 1 |
Entamoeba histolytica | phosphoglycerate mutase family protein, putative | 0.1577 | 0.4924 | 0.5 |
Mycobacterium ulcerans | hypothetical protein | 0.1577 | 0.4924 | 1 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.2673 | 1 | 1 |
Mycobacterium ulcerans | fructose-2,6-bisphosphatase GpmB | 0.1577 | 0.4924 | 1 |
Giardia lamblia | Hypothetical protein | 0.1577 | 0.4924 | 0.5 |
Schistosoma mansoni | 6-phosphofructokinase | 0.2673 | 1 | 1 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase 1 | 0.2628 | 0.9791 | 0.9706 |
Giardia lamblia | Hypothetical protein | 0.1577 | 0.4924 | 0.5 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.2673 | 1 | 1 |
Trypanosoma cruzi | 6-phosphofructo-2-kinase 1 | 0.2628 | 0.9791 | 0.9706 |
Loa Loa (eye worm) | hypothetical protein | 0.2673 | 1 | 1 |
Onchocerca volvulus | 0.2673 | 1 | 1 | |
Brugia malayi | TspO/MBR family protein | 0.0515 | 0 | 0.5 |
Trypanosoma brucei | 6-phosphofructo-2-kinase 2 | 0.2628 | 0.9791 | 0.9706 |
Leishmania major | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative | 0.2673 | 1 | 1 |
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.