class name | count |
---|---|
rosids | 25 |
asterids | 5 |
Liliopsida | 5 |
eudicotyledons | 1 |
Euphyllophyta | 1 |
class name | count |
---|---|
Fabaceae | 12 |
Connaraceae | 4 |
Moraceae | 4 |
Euphorbiaceae | 4 |
Hyacinthaceae | 4 |
Campanulaceae | 3 |
Bacillaceae | 2 |
Streptomycetaceae | 2 |
Solanaceae | 2 |
Commelinaceae | 1 |
Polygonaceae | 1 |
Paenibacillaceae | 1 |
Dryopteridaceae | 1 |
Myrtaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Piperidine alkaloids | 2 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Piperidine alkaloids | C10141 | C00002035 |
Piperidine alkaloids | C10144 | C00002038 |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P04062 | Glucosylceramidase | Enzyme | C00002035 C00002038 C00029420 C00036384 C00049941 C00049947 | 6 / 4 |
P04066 | Tissue alpha-L-fucosidase | Enzyme | C00002035 C00002038 C00029420 C00049941 C00049947 | 1 / 2 |
Q9HCG7 | Non-lysosomal glucosylceramidase | Enzyme | C00002035 C00002038 C00029420 C00049941 C00049947 | 1 / 0 |
Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002035 C00002038 C00029420 C00049941 C00049947 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002035 C00002038 C00029420 C00049941 C00049947 | 1 / 1 |
P35573 | Glycogen debranching enzyme | Enzyme | C00002035 C00029420 C00036384 C00036506 | 1 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002035 C00029420 C00036384 | 1 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002035 C00029420 C00036384 | 1 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002035 C00029420 C00036384 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002035 C00029420 C00036384 | 0 / 1 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00002035 C00029420 C00036384 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002035 C00029420 C00036384 | 0 / 1 |
Q6P4F1 | Alpha-(1,3)-fucosyltransferase 10 | Enzyme | C00002035 C00029420 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002035 C00029420 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002035 C00029420 | 2 / 5 |
Q9Y2E5 | Epididymis-specific alpha-mannosidase | Enzyme | C00002035 C00029420 | 0 / 0 |
P23458 | Tyrosine-protein kinase JAK1 | Jakb | C00002035 C00029420 | 0 / 0 |
P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00002035 C00029420 | 1 / 1 |
P06280 | Alpha-galactosidase A | Enzyme | C00002035 C00029420 | 1 / 1 |
O00754 | Lysosomal alpha-mannosidase | Enzyme | C00002035 C00029420 | 1 / 2 |
O00462 | Beta-mannosidase | Enzyme | C00002035 C00029420 | 1 / 2 |
P16278 | Beta-galactosidase | Enzyme | C00002035 C00029420 | 4 / 6 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002035 C00029420 | 3 / 1 |
P55055 | Oxysterols receptor LXR-beta | NR1H3 | C00002035 C00029420 | 0 / 0 |
P09848 | Lactase-phlorizin hydrolase | Enzyme | C00002035 C00029420 | 1 / 1 |
Q16739 | Ceramide glucosyltransferase | Transferase | C00002035 C00029420 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002035 C00029420 | 0 / 0 |
Q9H227 | Cytosolic beta-glucosidase | Enzyme | C00002035 C00029420 | 0 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00002035 C00029420 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002035 C00029420 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002035 C00029420 | 1 / 2 |
O43280 | Trehalase | Enzyme | C00002035 C00029420 | 0 / 0 |
Q13133 | Oxysterols receptor LXR-alpha | NR1H3 | C00002035 C00029420 | 0 / 0 |
P06737 | Glycogen phosphorylase, liver form | Enzyme | C00036384 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00036384 | 0 / 0 |
Q9UKM7 | Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase | Enzyme | C00036384 | 1 / 0 |
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
|
#230500 | Gm1-gangliosidosis, type i |
P16278
|
#230600 | Gm1-gangliosidosis, type ii |
P16278
|
#230650 | Gm1-gangliosidosis, type iii |
P16278
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#223000 | Lactase deficiency, congenital |
P09848
|
#248500 | Mannosidosis, alpha b, lysosomal; mansa |
O00754
|
#248510 | Mannosidosis, beta a, lysosomal; mansb |
O00462
|
#614202 | Mental retardation, autosomal recessive 15; mrt15 |
Q9UKM7
|
#253010 | Mucopolysaccharidosis type ivb |
P16278
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#614409 | Spastic paraplegia 46, autosomal recessive; spg46 |
Q9HCG7
|
#222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
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)
|
H00140 | beta-Mannosidosis |
O00462
(related)
|
H00422 | Glycoproteinoses |
O00462
(related)
O00754 (related) P04066 (related) P16278 (related) |
H00139 | alpha-Mannosidosis |
O00754
(related)
|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
P16278 (related) |
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00141 | Fucosidosis |
P04066
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P06737
(related)
P10253 (related) P35573 (related) |
H00036 | Osteosarcoma |
P08684
(marker)
|
H00116 | Congenital lactase deficiency |
P09848
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|
H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
H00276 | Galactosialidosis |
P16278
(related)
|
H00281 | GM1 gangliosidosis |
P16278
(related)
|
H00421 | Mucopolysaccharidosis (MPS) |
P16278
(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)
|