class name | count |
---|---|
rosids | 8 |
asterids | 5 |
class name | count |
---|---|
Nitrariaceae | 5 |
Acanthaceae | 3 |
Plantaginaceae | 1 |
Brassicaceae | 1 |
Apiaceae | 1 |
Biebersteiniaceae | 1 |
Malvaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Quinazoline alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Quinazoline alkaloids | C10744 | C00002202 |
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 |
---|---|---|---|---|---|---|
C00002150
![]() |
Deoxyvasicinone
|
CHEMBL456881
|
C025696
|
25 / 13 / 9 |
![]() |
|
C00002202
![]() |
Vasicinone
|
CHEMBL1864065
|
C052548
|
1 / 0 / 0 |
![]() |
|
C00026253
![]() |
Vasicinolone
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UNA4 | DNA polymerase iota | Enzyme | C00002150 C00002202 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002150 | 3 / 3 |
Q99700 | Ataxin-2 | Unclassified protein | C00002150 | 1 / 1 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00002150 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002150 | 0 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002150 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002150 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00002150 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002150 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002150 | 0 / 0 |
P06276 | Cholinesterase | Hydrolase | C00002150 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002150 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002150 | 0 / 0 |
P22303 | Acetylcholinesterase | Hydrolase | C00002150 | 1 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002150 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002150 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002150 | 0 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002150 | 1 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002150 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002150 | 0 / 0 |
Q2TB90 | Putative hexokinase HKDC1 | Enzyme | C00002150 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002150 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002150 | 1 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002150 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00002150 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#114500 | Colorectal cancer; crc |
Q14191
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|