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)
|