| class name | count | 
|---|---|
| Liliopsida | 15 | 
| rosids | 6 | 
| asterids | 2 | 
| class name | count | 
|---|---|
| Hyacinthaceae | 9 | 
| Streptomycetaceae | 7 | 
| Fabaceae | 4 | 
| Araceae | 4 | 
| Euphorbiaceae | 2 | 
| Campanulaceae | 2 | 
| Stemonaceae | 2 | 
 
                  
                | br08003 Category | # of metabolite | 
|---|
| br08003 Category | KEGG ID | KNApSAcK ID | 
|---|
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00002037 C00017836 C00018617 C00018724 C00036713 C00036798 C00036799 C00042067 C00042220 | 0 / 0 | 
| P06280 | Alpha-galactosidase A | Enzyme | C00002037 C00036713 C00036798 C00036799 C00038412 C00038589 C00042067 C00042220 C00045586 | 1 / 1 | 
| P04066 | Tissue alpha-L-fucosidase | Enzyme | C00002037 C00036713 C00036798 C00036799 C00038412 C00038589 C00042067 C00042220 C00045586 | 1 / 2 | 
| P04062 | Glucosylceramidase | Enzyme | C00002037 C00036713 C00036798 C00036799 C00042067 C00042220 | 6 / 4 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002037 C00036713 C00036798 C00036799 C00042067 C00042220 | 1 / 1 | 
| Q8TET4 | Neutral alpha-glucosidase C | Enzyme | C00036713 C00036798 C00036799 C00042220 | 0 / 0 | 
| P35573 | Glycogen debranching enzyme | Enzyme | C00002037 C00042067 C00045536 | 1 / 1 | 
| Q9BTY2 | Plasma alpha-L-fucosidase | Enzyme | C00038412 C00038589 C00045586 | 0 / 0 | 
| Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002037 C00042067 | 0 / 0 | 
| Q9H227 | Cytosolic beta-glucosidase | Enzyme | C00002037 C00042067 | 0 / 0 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #301500 | Fabry disease | P06280 | 
| #230000 | Fucosidosis | P04066 | 
| #608013 | Gaucher disease, perinatal lethal | P04062 | 
| #230800 | Gaucher disease, type i | P04062 | 
| #230900 | Gaucher disease, type ii | P04062 | 
| #231000 | Gaucher disease, type iii | P04062 | 
| #231005 | Gaucher disease, type iiic | P04062 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #232400 | Glycogen storage disease iii | P35573 | 
| #168600 | Parkinson disease, late-onset; pd | P04062 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00066 | Lewy body dementia (LBD) | P04062
                            (related) | 
| H00126 | Gaucher disease | P04062
                            (related) | 
| H00426 | Defects in the degradation of ganglioside | P04062
                            (related) | 
| H00810 | Progressive myoclonic epilepsy (PME) | P04062
                            (related) | 
| H00141 | Fucosidosis | P04066
                            (related) | 
| H00422 | Glycoproteinoses | P04066
                            (related) | 
| H00125 | Fabry disease | P06280
                            (related) | 
| H00069 | Glycogen storage diseases (GSD) | P10253
                            (related) P35573 (related) |