Angylocalyx pynaertii
Species
KNApSAcK Entry
| Organism name | Angylocalyx pynaertii |
|---|---|
| Genus | Angylocalyx |
| Family | Fabaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Angylocalyx pynaertii |
|---|---|
| Linked NCBI taxonomy ID | 149630 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | rosids |
|---|---|
| ID | 71275 |
Metabolite list (5)
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
C00038589
|
beta-L-Homofuconojirimycin
|
CHEMBL69294
CHEMBL87474 CHEMBL503021 |
3 / 2 / 3 | No. 667 |
|
|||
|
C00002038
|
Fagomine
|
CHEMBL303545
CHEMBL108084 CHEMBL456583 CHEMBL505237 CHEMBL1818435 CHEMBL1818436 CHEMBL1818437 CHEMBL1818438 CHEMBL1818439 |
C105643
|
5 / 9 / 7 | No. 786 | No. 1 |
|
|
|
C00045174
|
2-O-beta-D-glucopyranosyl 1,4-Dideoxy-1,4-imino-D-arabinitol
/ 1,4-Dideoxy-1,4-imino-(2-O-beta-D-glucopyranosyl)-D-arabinitol |
CHEMBL470268
|
No. 2052 |
|
||||
|
C00045359
|
N-Methyl 1,4-Dideoxy-1,4-imino-D-arabinitol
|
CHEMBL80148
|
1 / 0 / 0 | No. 4946 |
|
|||
|
C00045360
|
N-Methyl 1-Deoxymannojirimycin
|
CHEMBL418746
CHEMBL75971 |
4 / 4 / 3 | No. 4946 |
|
Human Protein / Gene in interactions
9 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04066 | Tissue alpha-L-fucosidase | Enzyme | C00002038 C00038589 C00045360 | 1 / 2 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00045359 C00045360 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002038 C00045360 | 1 / 1 |
| Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002038 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00002038 | 6 / 4 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00045360 | 2 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00038589 | 1 / 1 |
| Q9HCG7 | Non-lysosomal glucosylceramidase | Enzyme | C00002038 | 1 / 0 |
| Q9BTY2 | Plasma alpha-L-fucosidase | Enzyme | C00038589 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (12)
| 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
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #614409 | Spastic paraplegia 46, autosomal recessive; spg46 |
Q9HCG7
|
KEGG DISEASE (8)
| 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)
|