Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | v-akt murine thymoma viral oncogene homolog 1 | Starlite/ChEMBL | No references |
Homo sapiens | v-akt murine thymoma viral oncogene homolog 2 | Starlite/ChEMBL | No references |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | peptidase family M13 containing protein | 0.0143 | 0.6863 | 0.655 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Schistosoma mansoni | family M13 unassigned peptidase (M13 family) | 0.0098 | 0.4046 | 0.345 |
Loa Loa (eye worm) | hypothetical protein | 0.0143 | 0.6863 | 0.655 |
Trypanosoma cruzi | rac serine-threonine kinase, putative | 0.0061 | 0.1752 | 1 |
Schistosoma mansoni | neprilysin | 0.0051 | 0.1119 | 0.023 |
Entamoeba histolytica | protein kinase, putative | 0.009 | 0.3576 | 1 |
Trypanosoma brucei | rac serine-threonine kinase, putative | 0.009 | 0.3576 | 0.5 |
Toxoplasma gondii | peptidase family M13 protein | 0.0194 | 1 | 1 |
Echinococcus granulosus | calcium:calmodulin dependent protein kinase | 0.0058 | 0.1599 | 0.0048 |
Loa Loa (eye worm) | hypothetical protein | 0.0143 | 0.6863 | 0.655 |
Entamoeba histolytica | PH domain containing protein kinase, putative | 0.0061 | 0.1752 | 0.0776 |
Loa Loa (eye worm) | peptidase family M13 containing protein | 0.0143 | 0.6863 | 0.655 |
Schistosoma mansoni | serine/threonine-protein kinase | 0.0061 | 0.1752 | 0.0927 |
Mycobacterium tuberculosis | Probable zinc metalloprotease Zmp1 | 0.0194 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Brugia malayi | Protein kinase domain containing protein | 0.009 | 0.3576 | 0.2934 |
Plasmodium falciparum | RAC-beta serine/threonine protein kinase | 0.0058 | 0.1599 | 0.5 |
Schistosoma mansoni | family M13 unassigned peptidase (M13 family) | 0.0051 | 0.1119 | 0.023 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Loa Loa (eye worm) | hypothetical protein | 0.0194 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Schistosoma mansoni | family M13 non-peptidase homologue (M13 family) | 0.0098 | 0.4046 | 0.345 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Echinococcus granulosus | serine threonine protein kinase nrc | 0.0058 | 0.1599 | 0.0048 |
Brugia malayi | p70 ribosomal S6 kinase beta | 0.0088 | 0.3423 | 0.2765 |
Onchocerca volvulus | 0.0096 | 0.3936 | 0.5 | |
Loa Loa (eye worm) | AGC/RSK/P70 protein kinase | 0.0088 | 0.3423 | 0.2765 |
Schistosoma mansoni | neprilysin-2 (M13 family) | 0.0098 | 0.4046 | 0.345 |
Loa Loa (eye worm) | AGC/AKT protein kinase | 0.009 | 0.3576 | 0.2934 |
Echinococcus granulosus | endothelin converting enzyme 1 | 0.0194 | 1 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Giardia lamblia | Kinase, AGC PKA | 0.0058 | 0.1599 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0194 | 1 | 1 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Entamoeba histolytica | protein kinase, putative | 0.0088 | 0.3423 | 0.9224 |
Loa Loa (eye worm) | hypothetical protein | 0.0096 | 0.3936 | 0.3329 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Echinococcus multilocularis | endothelin converting enzyme 1 | 0.0194 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Entamoeba histolytica | PH domain containing protein kinase, putative | 0.0061 | 0.1752 | 0.0776 |
Schistosoma mansoni | hypothetical protein | 0.0051 | 0.1119 | 0.023 |
Schistosoma mansoni | family M13 unassigned peptidase (M13 family) | 0.0194 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0194 | 1 | 1 |
Brugia malayi | Hypothetical zinc metalloproteinase T16A9.4 | 0.0194 | 1 | 1 |
Echinococcus multilocularis | serine threonine protein kinase nrc serine threonine protein kinase gad | 0.0058 | 0.1599 | 0.0048 |
Echinococcus multilocularis | rac serine:threonine kinase | 0.0061 | 0.1752 | 0.0229 |
Plasmodium vivax | rac-beta serine/threonine protein kinase, putative | 0.0058 | 0.1599 | 0.5 |
Trichomonas vaginalis | AGC family protein kinase | 0.009 | 0.3576 | 1 |
Echinococcus granulosus | serine/threonine protein kinase | 0.0061 | 0.1752 | 0.0229 |
Mycobacterium leprae | probable zinc metalloprotease | 0.0194 | 1 | 0.5 |
Schistosoma mansoni | family M13 unassigned peptidase (M13 family) | 0.0098 | 0.4046 | 0.345 |
Trypanosoma cruzi | Protein kinase B | 0.0061 | 0.1752 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0147 | 0.7073 | 0.678 |
Loa Loa (eye worm) | hypothetical protein | 0.0143 | 0.6863 | 0.655 |
Schistosoma mansoni | Nep2 peptidase (M13 family) | 0.0098 | 0.4046 | 0.345 |
Mycobacterium ulcerans | zinc metalloprotease | 0.0194 | 1 | 0.5 |
Schistosoma mansoni | serine/threonine-protein kinase | 0.0061 | 0.1752 | 0.0927 |
Entamoeba histolytica | protein kinase, putative | 0.009 | 0.3576 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0143 | 0.6863 | 0.655 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 46 nM | BindingDB_Patents: TR-FRET Assay. For the assay 50 nl of a 100 fold concentrated solution of the test compound in DMSO was pipetted into a black low volume 384 well microtiter plate (Greiner Bio-One, Frickenhausen, Germany), 2 ul of a solution of Akt2 in assay buffer [50 mM TRIS/HCl pH 7.5, 5 mM MgCl2, 1 mM dithiothreitol, 0.02% (v/v) Triton X-100 (Sigma)] were added and the mixture was incubated for 15 min at 22 C. to allow prebinding of the test compounds to the enzyme before the start of the kinase reaction. Then the kinase reaction was started by the addition of 3 ul of a solution of adenosine-tri-phosphate (ATP, 16.7 uM=>final conc. in the 5 ul assay volume is 10 uM) and substrate (1.67 uM=>final conc. in the 5 ul assay volume is 1 uM) in assay buffer and the resulting mixture was incubated for a reaction time of 60 min at 22 C. The concentration of Akt2 in the assay was adjusted depending of the activity of the enzyme lot. | ChEMBL. | No reference |
IC50 (binding) | = 46 nM | BindingDB_Patents: TR-FRET Assay. For the assay 50 nl of a 100 fold concentrated solution of the test compound in DMSO was pipetted into a black low volume 384 well microtiter plate (Greiner Bio-One, Frickenhausen, Germany), 2 ul of a solution of Akt2 in assay buffer [50 mM TRIS/HCl pH 7.5, 5 mM MgCl2, 1 mM dithiothreitol, 0.02% (v/v) Triton X-100 (Sigma)] were added and the mixture was incubated for 15 min at 22 C. to allow prebinding of the test compounds to the enzyme before the start of the kinase reaction. Then the kinase reaction was started by the addition of 3 ul of a solution of adenosine-tri-phosphate (ATP, 16.7 uM=>final conc. in the 5 ul assay volume is 10 uM) and substrate (1.67 uM=>final conc. in the 5 ul assay volume is 1 uM) in assay buffer and the resulting mixture was incubated for a reaction time of 60 min at 22 C. The concentration of Akt2 in the assay was adjusted depending of the activity of the enzyme lot. | ChEMBL. | No reference |
IC50 (binding) | = 601 nM | BindingDB_Patents: TR-FRET Assay. For the assay 50 nl of a 100 fold concentrated solution of the test compound in DMSO was pipetted into a black low volume 384 well microtiter plate (Greiner Bio-One, Frickenhausen, Germany), 2 ul of a solution of Akt1 in assay buffer [50 mM TRIS/HCl pH 7.5, 5 mM MgCl2, 1 mM dithiothreitol, 0.02% (v/v) Triton X-100 (Sigma)] were added and the mixture was incubated for 15 min at 22 C. to allow prebinding of the test compounds to the enzyme before the start of the kinase reaction. Then the kinase reaction was started by the addition of 3 ul of a solution of adenosine-tri-phosphate (ATP, 16.7 uM=>final conc. in the 5 ul assay volume is 10 uM) and substrate (1.67 uM=>final conc. in the 5 ul assay volume is 1 uM) in assay buffer and the resulting mixture was incubated for a reaction time of 60 min at 22 C. The concentration of Akt1 in the assay was adjusted depending of the activity of the enzyme lot. | ChEMBL. | No reference |
IC50 (binding) | = 601 nM | BindingDB_Patents: TR-FRET Assay. For the assay 50 nl of a 100 fold concentrated solution of the test compound in DMSO was pipetted into a black low volume 384 well microtiter plate (Greiner Bio-One, Frickenhausen, Germany), 2 ul of a solution of Akt1 in assay buffer [50 mM TRIS/HCl pH 7.5, 5 mM MgCl2, 1 mM dithiothreitol, 0.02% (v/v) Triton X-100 (Sigma)] were added and the mixture was incubated for 15 min at 22 C. to allow prebinding of the test compounds to the enzyme before the start of the kinase reaction. Then the kinase reaction was started by the addition of 3 ul of a solution of adenosine-tri-phosphate (ATP, 16.7 uM=>final conc. in the 5 ul assay volume is 10 uM) and substrate (1.67 uM=>final conc. in the 5 ul assay volume is 1 uM) in assay buffer and the resulting mixture was incubated for a reaction time of 60 min at 22 C. The concentration of Akt1 in the assay was adjusted depending of the activity of the enzyme lot. | ChEMBL. | No reference |
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.