class name | count |
---|---|
rosids | 9 |
asterids | 1 |
class name | count |
---|---|
Fabaceae | 8 |
Solanaceae | 1 |
Enterobacteriaceae | 1 |
Brassicaceae | 1 |
Bacillaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00001340
![]() |
L-Arginine
|
CHEMBL212301
CHEMBL1485 |
22 / 12 / 16 |
![]() |
||
C00001364
![]() |
L-Homoarginine
|
CHEMBL589752
|
3 / 3 / 1 |
![]() |
||
C00001368
![]() |
gamma-Hydroxy-L-arginine
|
![]() |
||||
C00001369
![]() |
(+)-gamma-Hydroxy-L-homoarginine
|
![]() |
||||
C00017959
![]() |
N5-Hydroxy-L-arginine
/ delta-N-Hydroxy-L-arginine |
![]() |
||||
C00040829
![]() |
4-Hydroxyarginine
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P29475 | Nitric oxide synthase, brain | Enzyme | C00001340 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001340 | 1 / 0 |
Q9Y263 | Phospholipase A-2-activating protein | Unclassified protein | C00001364 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001340 | 3 / 2 |
Q15661 | Tryptase alpha/beta-1 | S1A | C00001340 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001340 | 0 / 1 |
O94760 | N(G),N(G)-dimethylarginine dimethylaminohydrolase 1 | Enzyme | C00001340 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00001340 | 0 / 0 |
P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00001364 | 0 / 0 |
P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00001364 | 3 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001340 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00001340 | 1 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001340 | 0 / 0 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00001340 | 0 / 0 |
P29474 | Nitric oxide synthase, endothelial | Enzyme | C00001340 | 0 / 0 |
P35228 | Nitric oxide synthase, inducible | Enzyme | C00001340 | 1 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001340 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001340 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001340 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001340 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001340 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00001340 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001340 | 1 / 2 |
Q9H015 | Solute carrier family 22 member 4 | Unclassified protein | C00001340 | 1 / 1 |
O76082 | Solute carrier family 22 member 5 | Unclassified protein | C00001340 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#212140 | Carnitine deficiency, systemic primary; cdsp |
O76082
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#301500 | Fabry disease |
P06280
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#146300 | Hypophosphatasia, adult |
P05186
|
#241510 | Hypophosphatasia, childhood |
P05186
|
#241500 | Hypophosphatasia, infantile |
P05186
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#611162 | Malaria, susceptibility to |
P35228
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#180300 | Rheumatoid arthritis; ra |
Q9H015
|
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)
|
H00286 | Crohn's disease |
O76082
(related)
Q9H015 (related) |
H00525 | Disorders of fatty-acid oxidation |
O76082
(related)
|
H00213 | Hypophosphatasia |
P05186
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00017 | Esophageal cancer |
P35228
(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)
|