Plant Species


Cumulative plant class count

class name count
rosids 4

Cumulative family count

class name count
Fabaceae 2
Brassicaceae 2
Enterobacteriaceae 2

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (3)

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
C00001346 External link 512 L-Canaline
CHEMBL1231652
C001926
C00001366 External link 512 L-Homoserine
CHEMBL11722
C00001393 External link 512 L-Serine
CHEMBL11298
CHEMBL285123
13 / 18 / 17

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001393 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001393 2 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001393 2 / 2
P02545 Prelamin-A/C Unclassified protein C00001393 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001393 0 / 1
P54132 Bloom syndrome protein Enzyme C00001393 1 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001393 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001393 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001393 0 / 1
Q7Z2H8 Proton-coupled amino acid transporter 1 Unclassified protein C00001393 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001393 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001393 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001393 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809

KEGG DISEASE (17)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (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)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)