EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
3.2.1.45 | AT3375 | - |
Homo sapiens | |
3.2.1.45 | conduritol B epoxide | - |
Homo sapiens |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
3.2.1.45 | lysosome | - |
Homo sapiens | 5764 | - |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
3.2.1.45 | Homo sapiens | P04062 | - |
- |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
3.2.1.45 | fibroblast | - |
Homo sapiens | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.2.1.45 | 3-amido-(Black Hole Quencher 2)-6-methoxytriazolyl-1'-ethyl-3'-amido-(boron-dipyrromethene 576/589) beta-D-glucopyranoside + H2O | - |
Homo sapiens | 6-methoxytriazolyl-1'-ethyl-3'-amido-(boron-dipyrromethene 576/589) beta-D-glucopyranoside + Black Hole Quencher 2-N-(3-hydroxypropyl)butanamide | - |
? | |
3.2.1.45 | 3-amido-[4-[[4-(dimethylamino)phenyl]azo]-benzoic acid]-L-6-methoxytriazol-5-[(2-azidoethyl)amino]naphthalene-1-sulfonic acid beta-D-glucopyranoside + H2O | - |
Homo sapiens | 6-O-[(1-[2-[(5-sulfonaphthalen-1-yl)amino]ethyl]-1H-1,2,3-triazol-4-yl)methyl]-beta-D-glucopyranose + 4-[(Z)-[4-(dimethylamino)phenyl]diazenyl]-N-(3-hydroxypropyl)benzamide | - |
? | |
3.2.1.45 | 4-methylumbelliferyl beta-D-glucoside + H2O | - |
Homo sapiens | 4-methylumbelliferone + beta-D-glucose | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
3.2.1.45 | acid beta-glucosidase | - |
Homo sapiens |
3.2.1.45 | GBA1 | - |
Homo sapiens |
3.2.1.45 | Gcase | - |
Homo sapiens |
3.2.1.45 | glucocerebrosidase | - |
Homo sapiens |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
3.2.1.45 | 5.5 | - |
- |
Homo sapiens |
EC Number | General Information | Comment | Organism |
---|---|---|---|
3.2.1.45 | malfunction | enzyme deficiency leads to abnormal accumulation of glucosyl ceramide in lysosomes and the development of the lysosomal storage disease known as Gauchers disease | Homo sapiens |