class name | count |
---|
class name | count |
---|---|
Streptomycetaceae | 3 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00017739
![]() |
1-epi-Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
4 / 8 / 6 |
![]() |
||
C00017740
![]() |
2-epi-Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
4 / 8 / 6 |
![]() |
||
C00018608
![]() |
Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
C043270
|
4 / 8 / 6 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P04062 | Glucosylceramidase | Enzyme | C00017739 C00017740 C00018608 | 6 / 4 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00017739 C00017740 C00018608 | 1 / 1 |
P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00017739 C00017740 C00018608 | 1 / 1 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00017739 C00017740 C00018608 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#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
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|