class name | count |
---|---|
rosids | 15 |
Liliopsida | 2 |
eudicotyledons | 2 |
Magnoliophyta | 1 |
class name | count |
---|---|
Anacardiaceae | 3 |
Aceraceae | 2 |
Combretaceae | 2 |
Euphorbiaceae | 2 |
Geraniaceae | 2 |
Crassulaceae | 1 |
Paeoniaceae | 1 |
Nymphaeaceae | 1 |
Dictyotaceae | 1 |
Lythraceae | 1 |
Betulaceae | 1 |
Begoniaceae | 1 |
Iridaceae | 1 |
Meliaceae | 1 |
Hypoxidaceae | 1 |
Rhodomelaceae | 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 |
---|---|---|---|---|---|---|
C00030222
![]() |
Progallin A
/ Ethyl gallate |
CHEMBL453196
|
C048734
|
![]() |
||
C00030754
![]() |
Methyl gallate
/ Methyl 3,4,5-trihydroxybenzoate |
CHEMBL65675
|
C052082
|
16 / 15 / 13 |
![]() |
|
C00031089
![]() |
Protocatechuic acid methyl ester
|
CHEMBL486027
|
7 / 3 / 5 |
![]() |
||
C00032950
![]() |
Ethyl protocatechuate
/ Ethyl 3,4-dihydroxybenzoate |
CHEMBL486216
|
C018063
|
7 / 3 / 5 |
![]() |
|
C00044447
![]() |
3-Bromo-4,5-dihydroxybenzoic acid methyl ester
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00031089 C00032950 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00031089 C00032950 | 0 / 1 |
P00915 | Carbonic anhydrase 1 | Lyase | C00031089 C00032950 | 0 / 0 |
P43166 | Carbonic anhydrase 7 | Lyase | C00031089 C00032950 | 0 / 0 |
O43570 | Carbonic anhydrase 12 | Lyase | C00031089 C00032950 | 1 / 2 |
P00918 | Carbonic anhydrase 2 | Lyase | C00031089 C00032950 | 1 / 2 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00030754 C00031089 | 1 / 1 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00030754 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00030754 | 11 / 10 |
P02768 | Serum albumin | Secreted protein | C00030754 | 0 / 0 |
Q9GZT9 | Egl nine homolog 1 | Enzyme | C00032950 | 1 / 1 |
P55789 | FAD-linked sulfhydryl oxidase ALR | Enzyme | C00030754 | 1 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00030754 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00030754 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00030754 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00030754 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00030754 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00030754 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00030754 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00030754 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00030754 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00030754 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00030754 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#609820 | Erythrocytosis, familial, 3; ecyt3 |
Q9GZT9
|
#232300 | Glycogen storage disease ii |
P10253
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#613076 | Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay |
P55789
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#278300 | Xanthinuria, type i |
P47989
|
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)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00236 | Congenital polycythemia |
Q9GZT9
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|