PCIDB

KCF-S cluster No. 4351 (2 metabolites)

Plant Species

Cumulative plant class count

class name count
rosids 3
Embryophyta 1
asterids 1

Cumulative family count

class name count
Fabaceae 2
Brassicaceae 1
Marchantiaceae 1
Ericaceae 1

KEGG BRITE br08003 External link 512

Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (2)

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
C00001120 External link 512 D-Galacturonic acid
CHEMBL496672
CHEMBL1159524
CHEMBL2068684
13 / 14 / 14
C00001123 External link 512 beta-D-glucuronic acid
CHEMBL496672
CHEMBL1159524
CHEMBL2068684
13 / 14 / 14

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 C00001120 C00001123 1 / 0
P02545 Prelamin-A/C Unclassified protein C00001120 C00001123 11 / 10
P02768 Serum albumin Secreted protein C00001120 C00001123 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001120 C00001123 0 / 1
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001120 C00001123 0 / 0
O75496 Geminin Unclassified protein C00001120 C00001123 0 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter C00001120 C00001123 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001120 C00001123 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001120 C00001123 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001120 C00001123 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00001120 C00001123 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001120 C00001123 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001120 C00001123 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#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
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (14)

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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)