| 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) |