Organism name | Alexa grandiflora |
---|---|
Genus | Alexa |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Alexa grandiflora |
---|---|
Linked NCBI taxonomy ID | 1079071 |
Linked level | species |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
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 |
---|---|---|---|---|---|---|---|---|
C00002028
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Castanospermine
|
CHEMBL67964
CHEMBL311226 CHEMBL421040 CHEMBL464490 CHEMBL1213468 CHEMBL1438313 CHEMBL1980354 |
C037806
|
14 / 13 / 16 | No. 677 | No. 2 |
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|
C00036643
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7a-Epialexaflorine
|
No. 677 | No. 2 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002028 | 1 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00002028 | 6 / 4 |
Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002028 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002028 | 1 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002028 | 0 / 1 |
O75496 | Geminin | Unclassified protein | C00002028 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002028 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002028 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002028 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002028 | 0 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002028 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002028 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002028 | 1 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002028 | 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
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|