class name | count |
---|
class name | count |
---|---|
Enterobacteriaceae | 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 |
---|---|---|---|---|---|---|
C00019561
![]() |
PPi
/ Diphosphoric acid / Pyrophosphoric acid |
CHEMBL1160571
|
C107241
|
10 / 5 / 7 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00019561 | 1 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00019561 | 0 / 1 |
P54132 | Bloom syndrome protein | Enzyme | C00019561 | 1 / 2 |
P00480 | Ornithine carbamoyltransferase, mitochondrial | Enzyme | C00019561 | 1 / 1 |
P14324 | Farnesyl pyrophosphate synthase | Transferase | C00019561 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00019561 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00019561 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00019561 | 0 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00019561 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00019561 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#210900 | Bloom syndrome; blm |
P54132
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#311250 | Ornithine transcarbamylase deficiency, hyperammonemia due to |
P00480
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
KEGG | name | UniProt |
---|---|---|
H00187 | Ornithine transcarbamylase deficiency |
P00480
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|