class name | count |
---|---|
rosids | 3 |
Liliopsida | 1 |
class name | count |
---|---|
Enterobacteriaceae | 4 |
Brassicaceae | 3 |
Poaceae | 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 |
---|---|---|---|---|---|---|
C00000123
![]() |
2-phosphoglycerate
/ D-2-Phosphoglyceric acid |
![]() |
||||
C00007286
![]() |
3-Phosphoglycerate
|
CHEMBL87788
CHEMBL1160563 |
C005156
|
2 / 1 / 1 |
![]() |
|
C00007287
![]() |
3-Phosphoserine
|
CHEMBL284377
CHEMBL1418244 |
C046162
|
20 / 11 / 11 |
![]() |
|
C00007385
![]() |
O-Phospho-L-homoserine
|
![]() |
||||
C00019551
![]() |
D-3-Phosphoglyceric acid
|
CHEMBL87788
CHEMBL1160563 |
2 / 1 / 1 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P00558 | Phosphoglycerate kinase 1 | Enzyme | C00007286 C00019551 | 1 / 1 |
P07205 | Phosphoglycerate kinase 2 | Enzyme | C00007286 C00019551 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00007287 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00007287 | 3 / 1 |
P00918 | Carbonic anhydrase 2 | Lyase | C00007287 | 1 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00007287 | 0 / 1 |
Q14831 | Metabotropic glutamate receptor 7 | Metabotropic glutamate receptor | C00007287 | 0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | C00007287 | 1 / 2 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00007287 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00007287 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00007287 | 0 / 0 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00007287 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00007287 | 0 / 1 |
Q04609 | Glutamate carboxypeptidase 2 | M28B | C00007287 | 0 / 0 |
Q14833 | Metabotropic glutamate receptor 4 | Metabotropic glutamate receptor | C00007287 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00007287 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00007287 | 0 / 1 |
P22748 | Carbonic anhydrase 4 | Lyase | C00007287 | 1 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00007287 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00007287 | 1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00007287 | 2 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00007287 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#210900 | Bloom syndrome; blm |
P54132
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#300653 | Phosphoglycerate kinase 1 deficiency |
P00558
|
#600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
KEGG | name | UniProt |
---|---|---|
H00664 | Anemia due to disorders of glycolytic enzymes |
P00558
(related)
|
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00021 | Renal cell carcinoma |
Q16790
(marker)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|