KCF-S cluster No. 2578 (4 metabolites)

Corresponding Phytochemical cluster No. 9


KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Phenylalanine derived alkaloids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Phenylalanine derived alkaloids C08301 C00001406

Metabolite list (4)

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 External link 512 Phenylglyoxal
CHEMBL233632
D010658
5 / 1 / 1 3 / 0
C00001406 External link 512 D-Cathinone
CHEMBL1124
CHEMBL2104047
1 / 0 / 0
C00002685 External link 512 Acetophenone
CHEMBL274467
C038699
2 / 0 / 0 2 / 0
C00042277 External link 512 Benzamide
CHEMBL267373
19 / 19 / 15

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

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

5 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

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 DISEASE (15)

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)