| 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)
|