class name | count |
---|---|
rosids | 47 |
asterids | 36 |
Liliopsida | 14 |
Magnoliophyta | 10 |
eudicotyledons | 7 |
Spermatophyta | 5 |
Euphyllophyta | 1 |
Embryophyta | 1 |
class name | count |
---|---|
Rutaceae
![]() |
9 |
Asteraceae
![]() |
8 |
Malvaceae
![]() |
6 |
Plantaginaceae
![]() |
6 |
Fabaceae
![]() |
5 |
Lamiaceae
![]() |
4 |
Bignoniaceae
![]() |
4 |
Piperaceae
![]() |
4 |
Rosaceae
![]() |
4 |
Apiaceae
![]() |
3 |
Rhamnaceae
![]() |
3 |
Pinaceae
![]() |
3 |
Aristolochiaceae
![]() |
3 |
Celastraceae
![]() |
3 |
Hypoxidaceae
![]() |
2 |
Lauraceae
![]() |
2 |
Euphorbiaceae
![]() |
2 |
Rubiaceae
![]() |
2 |
Posidoniaceae
![]() |
2 |
Asparagaceae
![]() |
2 |
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 |
---|---|---|---|---|---|---|
C00002674
![]() |
Syringic acid
/ 4-Hydroxy-3,5-dimethoxybenzoic acid |
CHEMBL1414
|
C001945
|
12 / 3 / 5 |
![]() |
|
C00002682
![]() |
Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid |
CHEMBL120568
|
D014641
|
5 / 3 / 3 | 5 / 0 |
![]() |
C00029476
![]() |
Eudesmic acid
/ Trimethylgallic acid / 3,4,5-Trimethoxybenzoic acid |
CHEMBL377172
|
C005854
|
3 / 2 / 2 |
![]() |
|
C00029479
![]() |
Veratric acid
/ 3,4-dimethoxybenzoic acid |
CHEMBL118903
|
C009333
|
10 / 6 / 6 |
![]() |
|
C00029502
![]() |
3-Hydroxy-4-methoxybenzoic acid
|
CHEMBL88700
|
C045317
|
2 / 1 / 4 |
![]() |
|
C00034769
![]() |
4-Hydroxy-2-methoxybenzoic acid
|
![]() |
||||
C00035926
![]() |
3,4-dimethoxybenzoic acid
|
CHEMBL118903
|
C009333
|
10 / 6 / 6 |
![]() |
|
C00035948
![]() |
4-Ethoxy-3-methoxybenzoic acid
|
CHEMBL1363623
|
7 / 12 / 8 |
![]() |
||
C00040794
![]() |
2,6-Dimethoxy-benzoic acid
|
CHEMBL488609
|
C472445
|
6 / 2 / 4 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00002674 C00029479 C00035926 C00040794 | 0 / 0 |
P51580 | Thiopurine S-methyltransferase | Enzyme | C00002682 C00029479 C00029502 C00035926 | 1 / 1 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00002674 C00029479 C00035926 C00040794 | 0 / 1 |
P00915 | Carbonic anhydrase 1 | Lyase | C00002674 C00029479 C00035926 C00040794 | 0 / 0 |
P43166 | Carbonic anhydrase 7 | Lyase | C00002674 C00029479 C00035926 C00040794 | 0 / 0 |
P00918 | Carbonic anhydrase 2 | Lyase | C00002674 C00029479 C00035926 C00040794 | 1 / 2 |
O43570 | Carbonic anhydrase 12 | Lyase | C00002674 C00029479 C00035926 C00040794 | 1 / 2 |
P22748 | Carbonic anhydrase 4 | Lyase | C00002674 C00029479 C00035926 | 1 / 1 |
P23280 | Carbonic anhydrase 6 | Lyase | C00002674 C00029479 C00035926 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00029479 C00035926 | 2 / 0 |
P15121 | Aldose reductase | Enzyme | C00002674 C00002682 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00002682 | 1 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00035948 | 0 / 1 |
O75496 | Geminin | Unclassified protein | C00029476 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00035948 | 3 / 2 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00002674 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00035948 | 7 / 3 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00029476 | 0 / 0 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00029476 | 2 / 2 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00035948 | 0 / 0 |
Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00002674 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00002682 | 1 / 1 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00029502 | 0 / 3 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00035948 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00035948 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002682 | 0 / 0 |
P07451 | Carbonic anhydrase 3 | Lyase | C00002674 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00035948 | 1 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
4846 | NOS3, ECNOS, eNOS | nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) |
C00002682
|
54575 | UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J | UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) |
C00002682
|
54659 | UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C | UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) |
C00002682
|
54577 | UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G | UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) |
C00002682
|
54576 | UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H | UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) |
C00002682
|
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#114500 | Colorectal cancer; crc |
P84022
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#615363 | Estrogen resistance; estrr |
P03372
|
#143100 | Huntington disease; hd |
P42858
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
#610460 | Thiopurine s-methyltransferase deficiency |
P51580
|
KEGG | name | UniProt |
---|---|---|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00964 | Thiopurine S-methyltransferase deficiency (TPMT deficiency) |
P51580
(related)
|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|