Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Mycobacterium tuberculosis | Probable 1-deoxy-D-xylulose 5-phosphate reductoisomerase Dxr (DXP reductoisomerase) (1-deoxyxylulose-5-phosphate reductoisomeras | References | |
Escherichia coli | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Wolbachia endosymbiont of Brugia malayi | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | 0.101974 | 0.5 | 0.5 |
Treponema pallidum | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | 0.101974 | 0.5 | 0.5 |
Mycobacterium leprae | PROBABLE 1-DEOXY-D-XYLULOSE 5-PHOSPHATE REDUCTOISOMERASE DXR (DXP REDUCTOISOMERASE) (1-DEOXYXYLULOSE-5-PHOSPHATE REDUCTOISOMERAS | 0.101974 | 0.5 | 0.5 |
Plasmodium vivax | 1-deoxy-D-xylulose 5-phosphate reductoisomerase, putative | 0.101974 | 0.5 | 0.5 |
Toxoplasma gondii | 1-deoxy-D-xylulose 5-phosphate reductoisomerase, putative | 0.101974 | 0.5 | 0.5 |
Plasmodium falciparum | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | 0.101974 | 0.5 | 0.5 |
Mycobacterium ulcerans | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | 0.101974 | 0.5 | 0.5 |
Chlamydia trachomatis | 1-deoxy-D-xylulose 5-phosphate reductoisomerase | 0.101974 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 0.028 uM | Antimalarial activity against Plasmodium falciparum Dd2 | ChEMBL. | 16439126 |
IC50 (functional) | = 0.028 uM | Antimalarial activity against Plasmodium falciparum Dd2 | ChEMBL. | 16439126 |
IC50 (binding) | = 0.059 uM | Inhibition of recombinant Escherichia coli DXR | ChEMBL. | 16439126 |
IC50 (binding) | = 0.059 uM | Inhibition of Escherichia coli DXR | ChEMBL. | 17583502 |
IC50 (binding) | = 0.059 uM | Inhibition of recombinant Escherichia coli DXR | ChEMBL. | 16439126 |
IC50 (binding) | = 0.059 uM | Inhibition of Escherichia coli DXR | ChEMBL. | 21379374 |
IC50 (functional) | = 0.09 uM | Antimalarial activity against Plasmodium falciparum 3D7 | ChEMBL. | 16439126 |
IC50 (functional) | = 0.09 uM | Antimalarial activity against Plasmodium falciparum 3D7 | ChEMBL. | 16439126 |
IC50 (functional) | = 0.6 uM | Antiplasmodial activity against Plasmodium falciparum Ghana by micro dilution assay | ChEMBL. | 20568776 |
Inhibition (functional) | = 46 % | Antiplasmodial activity against Plasmodium berghei ANKA infected in mice (Mus musculus) assessed as suppression of parasitaemia at 50 mg/kg, intraperitoneal for 5 consecutive days measured on day 4 post parasitic infection | ChEMBL. | 20568776 |
Kd (binding) | = 0.12 uM | Binding affinity to Mycobacterium tuberculosis DXR assessed as dissociation constant by spectrofluorimetric analysis in presence of NADPH and MnCl2 | ChEMBL. | 23819803 |
Ki (binding) | = 1.2 uM | Inhibition of Mycobacterium tuberculosis recombinant DXR expressed in Escherichia coli BL21 (DE3) using DXP as substrate and MgCl2 as cofactor preincubated for 10 mins | ChEMBL. | 21561155 |
MST (functional) | = 7 day | Antiplasmodial activity against Plasmodium berghei ANKA infected in mice (Mus musculus) assessed as mean survival time at 50 mg/kg, intraperitoneal for 5 consecutive days | ChEMBL. | 20568776 |
Species name | Source | Reference | Is orphan |
---|---|---|---|
Plasmodium falciparum | ChEMBL23 | 16439126 |
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.
5 literature references were collected for this gene.