Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | intercellular adhesion molecule 1 | Starlite/ChEMBL | References |
Trypanosoma cruzi | trypanothione reductase, putative | Curated by TDR Targets | References |
Homo sapiens | selectin E | Starlite/ChEMBL | References |
Homo sapiens | vascular cell adhesion molecule 1 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Plasmodium falciparum | dihydrolipoyl dehydrogenase, apicoplast | trypanothione reductase, putative | 492 aa | 548 aa | 21.5 % |
Echinococcus granulosus | c4b binding protein beta chain | selectin E | 610 aa | 551 aa | 22.1 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Toxoplasma gondii | thioredoxin reductase | 0.0076 | 1 | 1 |
Plasmodium falciparum | dihydrolipoyl dehydrogenase, mitochondrial | 0.0026 | 0.1979 | 0.1966 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Mycobacterium leprae | DIHYDROLIPOAMIDE DEHYDROGENASE LPD (LIPOAMIDE REDUCTASE (NADH)) (LIPOYL DEHYDROGENASE) (DIHYDROLIPOYL DEHYDROGENASE) (DIAPHORASE | 0.0026 | 0.1979 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.0015 | 0.0128 | 0.0112 |
Brugia malayi | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain containing protein | 0.0019 | 0.085 | 0.0836 |
Wolbachia endosymbiont of Brugia malayi | dihydrolipoamide dehydrogenase E3 component | 0.0026 | 0.1979 | 0.5 |
Echinococcus multilocularis | C type lectin domian containing protein | 0.0014 | 0.0016 | 0.0016 |
Brugia malayi | GCC2 and GCC3 family protein | 0.0022 | 0.1256 | 0.1242 |
Plasmodium vivax | dihydrolipoyl dehydrogenase, apicoplast, putative | 0.0026 | 0.1979 | 0.1966 |
Plasmodium falciparum | thioredoxin reductase | 0.0026 | 0.1979 | 0.1966 |
Echinococcus granulosus | C type lectin domian containing protein | 0.0014 | 0.0016 | 0.0016 |
Echinococcus granulosus | c4b binding protein beta chain | 0.0014 | 0.0016 | 0.0016 |
Plasmodium falciparum | dihydrolipoyl dehydrogenase, apicoplast | 0.0026 | 0.1979 | 0.1966 |
Echinococcus multilocularis | thioredoxin glutathione reductase | 0.0076 | 1 | 1 |
Brugia malayi | Immunoglobulin I-set domain containing protein | 0.0015 | 0.0128 | 0.0112 |
Wolbachia endosymbiont of Brugia malayi | dihydrolipoamide dehydrogenase E3 component | 0.0026 | 0.1979 | 0.5 |
Plasmodium vivax | glutathione reductase, putative | 0.0076 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0018 | 0.0591 | 0.0575 |
Plasmodium falciparum | thioredoxin reductase | 0.0076 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0018 | 0.0591 | 0.0575 |
Echinococcus multilocularis | dihydrolipoamide dehydrogenase | 0.0026 | 0.1979 | 0.1979 |
Schistosoma mansoni | c4b-binding protein beta chain | 0.0014 | 0.0016 | 0.0016 |
Echinococcus multilocularis | roundabout 2 | 0.0018 | 0.0591 | 0.0591 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0022 | 0.1256 | 0.1242 |
Plasmodium vivax | thioredoxin reductase, putative | 0.0076 | 1 | 1 |
Trypanosoma cruzi | trypanothione reductase, putative | 0.0076 | 1 | 1 |
Brugia malayi | alpha keto acid dehydrogenase complex, E3 component, lipoamide dehydrogenase | 0.0019 | 0.085 | 0.0836 |
Trichomonas vaginalis | mercuric reductase, putative | 0.0026 | 0.1979 | 0.5 |
Treponema pallidum | NADH oxidase | 0.0026 | 0.1979 | 0.5 |
Leishmania major | trypanothione reductase | 0.0076 | 1 | 1 |
Echinococcus multilocularis | c4b binding protein beta chain | 0.0014 | 0.0016 | 0.0016 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Loa Loa (eye worm) | hypothetical protein | 0.0016 | 0.0273 | 0.0257 |
Toxoplasma gondii | NADPH-glutathione reductase | 0.0026 | 0.1979 | 0.1966 |
Toxoplasma gondii | pyruvate dehydrogenase complex subunit PDH-E3II | 0.0026 | 0.1979 | 0.1966 |
Echinococcus granulosus | roundabout 2 | 0.0018 | 0.0591 | 0.0591 |
Trypanosoma brucei | trypanothione reductase | 0.0076 | 1 | 1 |
Brugia malayi | Thioredoxin reductase | 0.0076 | 1 | 1 |
Brugia malayi | dihydrolipoyl dehydrogenase, mitochondrial precursor, putative | 0.0026 | 0.1979 | 0.1966 |
Echinococcus granulosus | dihydrolipoamide dehydrogenase | 0.0026 | 0.1979 | 0.1979 |
Mycobacterium ulcerans | dihydrolipoamide dehydrogenase | 0.0026 | 0.1979 | 0.5 |
Mycobacterium ulcerans | flavoprotein disulfide reductase | 0.0026 | 0.1979 | 0.5 |
Plasmodium falciparum | glutathione reductase | 0.0026 | 0.1979 | 0.1966 |
Plasmodium vivax | dihydrolipoyl dehydrogenase, mitochondrial, putative | 0.0026 | 0.1979 | 0.1966 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Loa Loa (eye worm) | TK/KIN16 protein kinase | 0.0015 | 0.0128 | 0.0112 |
Giardia lamblia | NADH oxidase lateral transfer candidate | 0.0026 | 0.1979 | 0.5 |
Loa Loa (eye worm) | glutathione reductase | 0.0076 | 1 | 1 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Plasmodium falciparum | glutathione reductase | 0.0076 | 1 | 1 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Echinococcus granulosus | neurotracting:lsamp:neurotrimin:obcam | 0.0015 | 0.0128 | 0.0128 |
Schistosoma mansoni | cell adhesion molecule | 0.0015 | 0.0128 | 0.0128 |
Echinococcus granulosus | thioredoxin glutathione reductase | 0.0076 | 1 | 1 |
Onchocerca volvulus | 0.0014 | 0.0016 | 0.5 | |
Mycobacterium ulcerans | dihydrolipoamide dehydrogenase, LpdB | 0.0026 | 0.1979 | 0.5 |
Chlamydia trachomatis | dihydrolipoyl dehydrogenase | 0.0026 | 0.1979 | 0.5 |
Mycobacterium tuberculosis | NADPH-dependent mycothiol reductase Mtr | 0.0076 | 1 | 1 |
Schistosoma mansoni | dihydrolipoamide dehydrogenase | 0.0026 | 0.1979 | 0.1979 |
Loa Loa (eye worm) | thioredoxin reductase | 0.0076 | 1 | 1 |
Trichomonas vaginalis | glutathione reductase, putative | 0.0026 | 0.1979 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 8 nM | Inhibition of selectin E in human endothelial cells | ChEMBL. | 11585452 |
IC50 (binding) | = 8 nM | Inhibition of selectin E in human endothelial cells | ChEMBL. | 11585452 |
IC50 (binding) | = 10 nM | Inhibition of intercellular adhesion molecule-1 (ICAM1) in human endothelial cells | ChEMBL. | 11585452 |
IC50 (binding) | = 10 nM | Inhibition of intercellular adhesion molecule-1 (ICAM1) in human endothelial cells | ChEMBL. | 11585452 |
IC50 (binding) | > 1000 nM | Inhibition of VCAM-1 in human endothelial cells | ChEMBL. | 11585452 |
IC50 (binding) | > 1000 nM | Inhibition of VCAM-1 in human endothelial cells | ChEMBL. | 11585452 |
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.