Species

KNApSAcK Entry

Organism name Agloonema treubii
Genus
Family
Kingdom

Metabolite list (1)

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
C00036798 External link 512 beta-Homomannojirimycin
CHEMBL87169
CHEMBL320116
CHEMBL327137
CHEMBL501355
CHEMBL1169500
CHEMBL2093079
CHEMBL2093897
CHEMBL2111688
CHEMBL2114210
CHEMBL2115215
6 / 9 / 8 No. 667

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00036798 6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase C00036798 1 / 1
P04066 Tissue alpha-L-fucosidase Enzyme C00036798 1 / 2
Q8TET4 Neutral alpha-glucosidase C Enzyme C00036798 0 / 0
P06280 Alpha-galactosidase A Enzyme C00036798 1 / 1
O43451 Maltase-glucoamylase, intestinal Hydrolase C00036798 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

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

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)