Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | tissue type plasminogen activator | 0.0089 | 0.1612 | 0.5 |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.0156 | 0.8318 | 0.8318 |
Schistosoma mansoni | hypothetical protein | 0.0089 | 0.1612 | 0.1138 |
Onchocerca volvulus | 0.0089 | 0.1612 | 0.1612 | |
Loa Loa (eye worm) | hypothetical protein | 0.0089 | 0.1612 | 0.1612 |
Onchocerca volvulus | 0.0156 | 0.8318 | 0.8318 | |
Loa Loa (eye worm) | hypothetical protein | 0.0086 | 0.1289 | 0.1289 |
Brugia malayi | SEA domain containing protein | 0.0156 | 0.8318 | 0.8318 |
Onchocerca volvulus | 0.0156 | 0.8318 | 0.8318 | |
Brugia malayi | Protein kinase domain containing protein | 0.0089 | 0.1612 | 0.1612 |
Schistosoma mansoni | hypothetical protein | 0.0156 | 0.8318 | 1 |
Trypanosoma cruzi | hypothetical protein, conserved | 0.0089 | 0.1612 | 0.5 |
Echinococcus multilocularis | tissue type plasminogen activator | 0.0089 | 0.1612 | 0.5 |
Leishmania major | hypothetical protein, conserved | 0.0089 | 0.1612 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0173 | 1 | 1 |
Onchocerca volvulus | 0.0156 | 0.8318 | 0.8318 | |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.0089 | 0.1612 | 0.5 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.0089 | 0.1612 | 0.5 |
Toxoplasma gondii | kringle domain-containing protein | 0.0089 | 0.1612 | 0.5 |
Brugia malayi | Kringle domain containing protein | 0.0089 | 0.1612 | 0.1612 |
Onchocerca volvulus | 0.0156 | 0.8318 | 0.8318 | |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.0089 | 0.1612 | 0.1612 |
Loa Loa (eye worm) | hypothetical protein | 0.0156 | 0.8318 | 0.8318 |
Onchocerca volvulus | 0.0173 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (binding) | Inhibition of RRM1 in human U2OS cells assessed as gammaH2AX induction at 0.5 to 125 uM after 2 hrs by FITC/propidium iodide-staining based flow cytometry in presence of SCH900776 | ChEMBL. | 24588962 | |
Inhibition (binding) | Inhibition of RRM1 in human U2OS cells assessed as gammaH2AX induction at 0.5 to 125 uM after 2 hrs by FITC/propidium iodide-staining based flow cytometry in absence of SCH900776 | ChEMBL. | 24588962 | |
Inhibition (binding) | Inhibition of RRM1 in human U2OS cells assessed as gammaH2AX induction after 2 hrs by FITC/propidium iodide-staining based flow cytometry in presence of SCH900776 | ChEMBL. | 24588962 |
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.