Organism name | Hyacinthoides non-scripta |
---|---|
Genus | Hyacinthoides |
Family | Hyacinthaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Hyacinthoides non-scripta |
---|---|
Linked NCBI taxonomy ID | 81762 |
Linked level | species |
Family in NCBI taxonomy | Hyacinthaceae |
---|---|
ID | 44985 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Liliopsida |
---|---|
ID | 4447 |
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
![]() |
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
![]() |
Hyacinthacine B1
/ (+)-Hyacinthacine B1 / (1S,2R,3R,5R,7aR)-1,2-Dihydroxy-3,5-dihydroxymethylpyrrolizidine |
No. 753 |
![]() |
|||||
C00036384
![]() |
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
![]() |
Homo-DMDP 7-O-beta-D-xylopyranoside
/ 2,5-Dideoxy-2,5-imino-DL-glycero-D-manno-heptitol 7-beta-D-xylopyranoside |
No. 2052 |
![]() |
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 |
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 | 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)
|