| class name | count |
|---|---|
| rosids | 16 |
| class name | count |
|---|---|
| Moraceae | 16 |
| 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 |
|---|---|---|---|---|---|---|
|
C00027960
|
Broussonetine C
|
CHEMBL1373221
|
4 / 7 / 5 |
|
||
|
C00027961
|
Broussonetine D
|
|
||||
|
C00027962
|
Broussonetine E
|
CHEMBL470659
|
|
|||
|
C00027963
|
Broussonetine F
|
CHEMBL470660
|
|
|||
|
C00027970
|
Broussonetinine A
|
CHEMBL1373221
|
4 / 7 / 5 |
|
||
|
C00027971
|
Broussonetinine B
|
|
||||
|
C00032771
|
Broussonetine M
/ (+)-Broussonetine M |
|
||||
|
C00032772
|
Broussonetine M1
/ (+)-Broussonetine M1 |
|
||||
|
C00032773
|
Broussonetine N
/ (+)-Broussonetine N |
|
||||
|
C00032774
|
Broussonetine O
/ (+)-Broussonetine O |
|
||||
|
C00032775
|
Broussonetine P
/ (+)-Broussonetine P |
|
||||
|
C00032778
|
Broussonetine S
/ (+)-Broussonetine S |
|
||||
|
C00032779
|
Broussonetine T
/ (+)-Broussonetine T |
|
||||
|
C00032780
|
Broussonetine U
/ (+)-Broussonetine U |
|
||||
|
C00032781
|
Broussonetine U1
/ (-)-Broussonetine U1 |
|
||||
|
C00032782
|
Broussonetine V
/ (+)-Broussonetine V |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00027960 C00027970 | 6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00027960 C00027970 | 1 / 1 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00027960 C00027970 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00027960 C00027970 | 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
|
| 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)
|