Species

KNApSAcK Entry

Organism name Hyacinthoides non-scripta
Genus Hyacinthoides
Family Hyacinthaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Hyacinthoides non-scripta
Linked NCBI taxonomy ID 81762
Linked level species

Family

Family in NCBI taxonomy Hyacinthaceae
ID 44985

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

Metabolite list (4)

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
C00002037 External link 512 DMDP
/ (+)-2,5-Dideoxy-2,5-imino-D-mannitol
/ 2R,5R-Dihydroxymethyl-3R,4R-dihydroxy-pyrrolidine
CHEMBL10437
CHEMBL312653
CHEMBL121093
CHEMBL259905
CHEMBL405957
CHEMBL469844
CHEMBL2008021
C043121
8 / 10 / 8 No. 667
C00037284 External link 512 Hyacinthacine B1
/ (+)-Hyacinthacine B1
/ (1S,2R,3R,5R,7aR)-1,2-Dihydroxy-3,5-dihydroxymethylpyrrolizidine
No. 753
C00036384 External link 512 D-AB1
/ 1,4-Dideoxy-1,4-imino-D-arabinitol
CHEMBL305131
CHEMBL80254
CHEMBL374349
CHEMBL261634
CHEMBL406973
CHEMBL1289018
CHEMBL1531321
13 / 12 / 9 No. 786 No. 1
C00036462 External link 512 Homo-DMDP 7-O-beta-D-xylopyranoside
/ 2,5-Dideoxy-2,5-imino-DL-glycero-D-manno-heptitol 7-beta-D-xylopyranoside
No. 2052

Human Protein / Gene in interactions

18 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00002037 C00036384 6 / 4
O43451 Maltase-glucoamylase, intestinal Hydrolase C00002037 C00036384 0 / 0
P35573 Glycogen debranching enzyme Enzyme C00002037 C00036384 1 / 1
Q9UKM7 Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase Enzyme C00036384 1 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002037 1 / 1
Q9H227 Cytosolic beta-glucosidase Enzyme C00002037 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00036384 1 / 0
P04066 Tissue alpha-L-fucosidase Enzyme C00002037 1 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00036384 0 / 1
Q14697 Neutral alpha-glucosidase AB Enzyme C00002037 0 / 0
O75496 Geminin Unclassified protein C00036384 0 / 0
P06737 Glycogen phosphorylase, liver form Enzyme C00036384 1 / 1
P06280 Alpha-galactosidase A Enzyme C00002037 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00036384 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00036384 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00036384 0 / 1
Q16706 Alpha-mannosidase 2 Enzyme C00036384 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00036384 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#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
#232400 Glycogen storage disease iii P35573
#232700 Glycogen storage disease vi P06737
#614202 Mental retardation, autosomal recessive 15; mrt15 Q9UKM7
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (12)

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) P06737 (related)
P10253 (related)
P35573 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)