| 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)
|