Organism name | Eugenia spp. |
---|---|
Genus | Eugenia |
Family | Myrtaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Eugenia |
---|---|
Linked NCBI taxonomy ID | 119950 |
Linked level | genus |
Family in NCBI taxonomy | Myrtaceae |
---|---|
ID | 3931 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
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 |
![]() |
||
C00002678
![]() |
Nasutin B
/ 3,3',4'-tri-O-methylellagic acid |
CHEMBL451476
|
No. 2068 | No. 81 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00036384 | 1 / 0 |
Q16706 | Alpha-mannosidase 2 | Enzyme | C00036384 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00036384 | 6 / 4 |
P35573 | Glycogen debranching enzyme | Enzyme | C00036384 | 1 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00036384 | 0 / 1 |
Q9UKM7 | Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase | Enzyme | C00036384 | 1 / 0 |
O75496 | Geminin | Unclassified protein | C00036384 | 0 / 0 |
P06737 | Glycogen phosphorylase, liver form | Enzyme | C00036384 | 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 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | 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
|
#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
|
#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)
|
H00069 | Glycogen storage diseases (GSD) |
P06737
(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)
|