KCF-S cluster No. 1523 (7 metabolites)

Corresponding Phytochemical cluster No. 1


Plant Species


Cumulative plant class count

class name count
rosids 8
Liliopsida 5
eudicotyledons 1

Cumulative family count

class name count
Fabaceae 6
Araceae 2
Asparagaceae 2
Brassicaceae 2
Hyacinthaceae 1
Amaranthaceae 1
Enterobacteriaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Piperidine alkaloids 1

metabolites link (2)

br08003 Category KEGG ID KNApSAcK ID
Piperidine alkaloids C00408 C00000210
Piperidine alkaloids C00408 C00001387

Metabolite list (7)

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
C00000210 External link 512 L-Pepecolic acid
CHEMBL308408
CHEMBL322883
CHEMBL1231898
3 / 0 / 3
C00001343 External link 512 L-Azetidine 2-carboxylic acid
CHEMBL33592
CHEMBL1165239
CHEMBL1599178
C089382
8 / 14 / 15
C00001370 External link 512 trans-4-Hydroxy-L-proline
CHEMBL352418
CHEMBL1213475
CHEMBL1229563
CHEMBL1233477
2 / 1 / 1
C00001387 External link 512 L-Pipecolic acid
CHEMBL308408
CHEMBL322883
CHEMBL1231898
C031345
3 / 0 / 3 1 / 1
C00001388 External link 512 L-Proline
CHEMBL54922
CHEMBL72275
CHEMBL80257
10 / 14 / 17
C00037000 External link 512 trans-5-Hydroxypipecolic acid
C00037104 External link 512 cis-5-Hydroxypipecolic acid

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q7Z2H8 Proton-coupled amino acid transporter 1 Unclassified protein C00000210 C00001343 C00001370 C00001387 C00001388 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001343 C00001388 1 / 0
P02545 Prelamin-A/C Unclassified protein C00001343 C00001388 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001343 C00001388 0 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000210 C00001387 0 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001343 C00001388 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001343 C00001388 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001343 C00001388 1 / 1
Q9P0Z9 Peroxisomal sarcosine oxidase Enzyme C00000210 C00001387 0 / 0
P54132 Bloom syndrome protein Enzyme C00001343 1 / 2
Q9GZT9 Egl nine homolog 1 Enzyme C00001370 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00001388 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00001388 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001388 1 / 4

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
51268 PIPOX, LPIPOX pipecolic acid oxidase (EC:1.5.3.1 1.5.3.7) C00001387

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

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
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#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
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (23)

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)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00236 Congenital polycythemia Q9GZT9 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D018901 Peroxisomal Disorders C00001387