class name | count |
---|---|
rosids | 8 |
asterids | 1 |
eudicotyledons | 1 |
class name | count |
---|---|
Celastraceae | 2 |
Cistaceae | 2 |
Salicaceae | 1 |
Euphorbiaceae | 1 |
Cyprinidae | 1 |
Convolvulaceae | 1 |
Proteaceae | 1 |
Urticaceae | 1 |
Apidae | 1 |
Rutaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Phenylalanine derived alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Phenylalanine derived alkaloids | C08301 | C00001406 |
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 |
---|---|---|---|---|---|---|
C00000211
![]() |
Phenylglyoxal
|
CHEMBL233632
|
D010658
|
5 / 1 / 1 | 3 / 0 |
![]() |
C00001406
![]() |
D-Cathinone
|
CHEMBL1124
CHEMBL2104047 |
1 / 0 / 0 |
![]() |
||
C00002685
![]() |
Acetophenone
|
CHEMBL274467
|
C038699
|
2 / 0 / 0 | 2 / 0 |
![]() |
C00042277
![]() |
Benzamide
|
CHEMBL267373
|
19 / 19 / 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000211 C00042277 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00000211 C00042277 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00000211 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00042277 | 3 / 2 |
P54132 | Bloom syndrome protein | Enzyme | C00042277 | 1 / 2 |
Q13464 | Rho-associated protein kinase 1 | Rock | C00002685 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00000211 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00042277 | 0 / 0 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00002685 | 0 / 0 |
P09874 | Poly [ADP-ribose] polymerase 1 | Enzyme | C00042277 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00042277 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00042277 | 0 / 0 |
Q86W56 | Poly(ADP-ribose) glycohydrolase | Enzyme | C00042277 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00042277 | 3 / 3 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00042277 | 5 / 2 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00000211 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00042277 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00042277 | 0 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00042277 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00042277 | 4 / 3 |
Q99549 | M-phase phosphoprotein 8 | Unclassified protein | C00042277 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00042277 | 1 / 1 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00042277 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00042277 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001406 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
217 | ALDH2, ALDH-E2, ALDHI, ALDM | aldehyde dehydrogenase 2 family (mitochondrial) (EC:1.2.1.3) |
C00002685
|
250 | ALPP, ALP, PALP, PLAP, PLAP-1 | alkaline phosphatase, placental (EC:3.1.3.1) |
C00002685
|
10327 | AKR1A1, ALDR1, ALR, ARM, DD3 | aldo-keto reductase family 1, member A1 (aldehyde reductase) (EC:1.1.1.2) |
C00000211
|
231 | AKR1B1, ADR, ALDR1, ALR2, AR | aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) |
C00000211
|
2530 | FUT8 | fucosyltransferase 8 (alpha (1,6) fucosyltransferase) (EC:2.4.1.68) |
C00000211
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#210900 | Bloom syndrome; blm |
P54132
|
#118300 | Charcot-marie-tooth disease and deafness |
Q01453
|
#118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a |
Q01453
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#139393 | Guillain-barre syndrome, familial; gbs |
Q01453
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#145900 | Hypertrophic neuropathy of dejerine-sottas |
Q01453
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
Q01453
(related)
|
H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) |
Q01453
(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)
|