Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | baculoviral IAP repeat containing 5 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Echinococcus multilocularis | baculoviral IAP repeat containing protein | Get druggable targets OG5_132424 | All targets in OG5_132424 |
Brugia malayi | Inhibitor of Apoptosis domain containing protein | Get druggable targets OG5_132424 | All targets in OG5_132424 |
Loa Loa (eye worm) | hypothetical protein | Get druggable targets OG5_132424 | All targets in OG5_132424 |
Echinococcus granulosus | baculoviral IAP repeat containing protein | Get druggable targets OG5_132424 | All targets in OG5_132424 |
Onchocerca volvulus | Deterin homolog | Get druggable targets OG5_132424 | All targets in OG5_132424 |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | baculoviral IAP repeat containing protein | 0.0357 | 1 | 1 |
Schistosoma mansoni | inhibitor of apoptosis protein | 0.0098 | 0.1359 | 0.5 |
Schistosoma mansoni | inhibitor of apoptosis (iap) domain family member | 0.0098 | 0.1359 | 0.5 |
Echinococcus granulosus | baculoviral IAP repeat containing protein | 0.0357 | 1 | 1 |
Trypanosoma cruzi | cytochrome P450, putative | 0.008 | 0.077 | 0.5 |
Loa Loa (eye worm) | cytochrome P450 family protein | 0.008 | 0.077 | 0.077 |
Loa Loa (eye worm) | hypothetical protein | 0.0098 | 0.1359 | 0.1359 |
Loa Loa (eye worm) | CYP4Cod1 | 0.008 | 0.077 | 0.077 |
Leishmania major | cytochrome p450-like protein | 0.008 | 0.077 | 0.5 |
Loa Loa (eye worm) | cytochrome P450 family protein | 0.008 | 0.077 | 0.077 |
Mycobacterium ulcerans | cytochrome P450 185A4 Cyp185A4 | 0.008 | 0.077 | 0.5 |
Brugia malayi | Inhibitor of Apoptosis domain containing protein | 0.0098 | 0.1359 | 0.0637 |
Trypanosoma brucei | cytochrome P450, putative | 0.008 | 0.077 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0098 | 0.1359 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0357 | 1 | 1 |
Trypanosoma cruzi | cytochrome P450, putative | 0.008 | 0.077 | 0.5 |
Onchocerca volvulus | Deterin homolog | 0.0357 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Kd (binding) | > 4.3 uM | Binding affinity to human survivin expressed in Escherichia coli BL21 cells after 30 mins | ChEMBL. | 17391963 |
Kd (binding) | > 4.3 uM | Binding affinity to human survivin expressed in Escherichia coli BL21 cells after 30 mins | ChEMBL. | 17391963 |
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.