Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | fucosidase, alpha-L- 1, tissue | Starlite/ChEMBL | References |
Bos taurus | Alpha-L-fucosidase 1 | Starlite/ChEMBL | References |
Rattus norvegicus | Alpha-L-fucosidase I | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target/s | Ortholog Group |
---|---|---|---|
Schistosoma mansoni | alpha-l-fucosidase | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Echinococcus granulosus | fucosidase alpha L 1 tissue | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Echinococcus multilocularis | fucosidase, alpha L 1, tissue | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Schistosoma japonicum | ko:K01206 alpha-L-fucosidase [EC3.2.1.51], putative | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Brugia malayi | Alpha-L-fucosidase family protein | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Mycobacterium ulcerans | alpha-L-fucosidase | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Loa Loa (eye worm) | alpha-L-fucosidase | Get druggable targets OG5_129683 | All targets in OG5_129683 |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Onchocerca volvulus | Alpha-L-fucosidase I | 462 aa | 422 aa | 44.8 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Brugia malayi | Alpha-L-fucosidase family protein | 0.125 | 0 | 0.5 |
Echinococcus multilocularis | fucosidase, alpha L 1, tissue | 0.1455 | 1 | 0.5 |
Schistosoma mansoni | alpha-l-fucosidase | 0.125 | 0 | 0.5 |
Mycobacterium ulcerans | alpha-L-fucosidase | 0.1455 | 1 | 0.5 |
Loa Loa (eye worm) | alpha-L-fucosidase | 0.125 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 0.035 uM | Inhibition of human lysosome alpha-L-fucosidase using 4-methylumbelliferyl-alpha-L-fucopyranoside by spectrophotometry | ChEMBL. | 24026016 |
IC50 (binding) | = 0.042 uM | Inhibition of bovine kidney alpha-L-fucosidase assessed as inhibition of release of p-nitrophenol by spectrophotometry | ChEMBL. | 24026016 |
IC50 (binding) | = 0.35 uM | Inhibition of rat epididymis alpha-L-fucosidase assessed as inhibition of release of p-nitrophenol by spectrophotometry | ChEMBL. | 24026016 |
IC50 (binding) | = 346 uM | Inhibition of bovine liver beta-galactosidase assessed as inhibition of p-nitrophenol release by spectrophotometry | ChEMBL. | 24026016 |
Inhibition (binding) | = 0 % | Inhibition of coffee beans alpha-galactosidase assessed as inhibition of p-nitrophenol release at 1000 uM by spectrophotometry | ChEMBL. | 24026016 |
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.