KCF-S cluster No. 1656 (6 metabolites)

Corresponding Phytochemical cluster No. 1


Plant Species


Cumulative plant class count

class name count
rosids 3

Cumulative family count

class name count
Enterobacteriaceae 4
Brassicaceae 3

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Pyridine alkaloids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Pyridine alkaloids C13051 C00007537

Metabolite list (6)

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
C00007256 External link 512 NAD
/ Nicotinamide adenine dinucleotide
CHEMBL234870
CHEMBL1234613
CHEMBL1402028
CHEMBL1454168
CHEMBL1517480
D009243
18 / 25 / 24 23 / 3
C00007537 External link 512 Nicotinic acid adenine dinucleotide
C024376
1 / 0
C00007538 External link 512 2'-O-Acetyl-ADP-ribose
C00019343 External link 512 NADH
/ Dihydronicotinamide adenine dinucleotide
CHEMBL1161866
2 / 0 / 0
C00019545 External link 512 TPNH
/ NADPH
CHEMBL407009
CHEMBL1594246
CHEMBL1619387
CHEMBL1623059
7 / 3 / 1
C00019568 External link 512 Nicotinic acid dinucleotide
C018348
1 / 0

Human Protein / Gene in interactions

23 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P49798 Regulator of G-protein signaling 4 Unclassified protein C00007256 C00019545 2 / 0
P07327 Alcohol dehydrogenase 1A Oxidoreductase C00007256 C00019343 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00007256 C00019545 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00007256 C00019545 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00019545 0 / 0
P02545 Prelamin-A/C Unclassified protein C00007256 11 / 10
P37840 Alpha-synuclein Unclassified protein C00007256 4 / 2
P12268 Inosine-5'-monophosphate dehydrogenase 2 Oxidoreductase C00007256 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00007256 2 / 3
P17405 Sphingomyelin phosphodiesterase Enzyme C00007256 2 / 2
Q92830 Histone acetyltransferase KAT2A Enzyme C00007256 0 / 0
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00019343 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00019545 0 / 0
P00338 L-lactate dehydrogenase A chain Enzyme C00007256 1 / 5
Q99700 Ataxin-2 Unclassified protein C00019545 1 / 1
P34981 Thyrotropin-releasing hormone receptor Neuropeptide receptor C00007256 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00007256 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00007256 0 / 0
P28329 Choline O-acetyltransferase Enzyme C00007256 1 / 1
O95544 NAD kinase Enzyme C00007256 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00019545 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007256 1 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007256 1 / 1

24 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
55191 NADSYN1 NAD synthetase 1 (EC:6.3.5.1) C00007256 C00019568
10495 ENOX2, APK1, COVA1, tNOX ecto-NOX disulfide-thiol exchanger 2 C00007256
10327 AKR1A1, ALDR1, ALR, ARM, DD3 aldo-keto reductase family 1, member A1 (aldehyde reductase) (EC:1.1.1.2) C00007256
216 ALDH1A1, ALDC, ALDH-E1, ALDH1, ALDH11, PUMB1, RALDH1 aldehyde dehydrogenase 1 family, member A1 (EC:1.2.1.36) C00007256
219 ALDH1B1, ALDH5, ALDHX aldehyde dehydrogenase 1 family, member B1 (EC:1.2.1.3) C00007256
217 ALDH2, ALDH-E2, ALDHI, ALDM aldehyde dehydrogenase 2 family (mitochondrial) (EC:1.2.1.3) C00007256
218 ALDH3A1, ALDH3, ALDHIII aldehyde dehydrogenase 3 family, member A1 (EC:1.2.1.5) C00007256
581 BAX, BCL2L4 BCL2-associated X protein C00007256
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00007256
847 CAT catalase (EC:1.11.1.6) C00007256
1050 CEBPA, C/EBP-alpha, CEBP CCAAT/enhancer binding protein (C/EBP), alpha C00007256
1727 CYB5R3, B5R, DIA1 cytochrome b5 reductase 3 (EC:1.6.2.2) C00007256
57192 MCOLN1, MG-2, ML4, MLIV, MST080, TRP-ML1, TRPM-L1, TRPML1 mucolipin 1 C00007537
2597 GAPDH, G3PD, GAPD glyceraldehyde-3-phosphate dehydrogenase (EC:1.2.1.12) C00007256
3033 HADH, HAD, HADH1, HADHSC, HCDH, HHF4, MSCHAD, SCHAD hydroxyacyl-CoA dehydrogenase (EC:1.1.1.35) C00007256
15461 C00007256
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00007256
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00007256
195814 SDR16C5, RDH#2, RDH-E2, RDHE2 short chain dehydrogenase/reductase family 16C, member 5 (EC:1.1.1.105) C00007256
23411 SIRT1, SIR2L1 sirtuin 1 C00007256
6610 SMPD2, ISC1, NSMASE, NSMASE1 sphingomyelin phosphodiesterase 2, neutral membrane (neutral sphingomyelinase) (EC:3.1.4.12) C00007256
8877 SPHK1, SPHK sphingosine kinase 1 (EC:2.7.1.91) C00007256
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00007256
7299 TYR, ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3 tyrosinase (EC:1.14.18.1) C00007256

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (26)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#127750 Dementia, lewy body; dlb P37840
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#612933 Glycogen storage disease xi; gsd11 P00338
#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
#254210 Myasthenic syndrome, congenital, associated with episodic apnea P28329
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (25)

KEGG name UniProt
H00069 Glycogen storage diseases (GSD) P00338 (related)
H00010 Multiple myeloma P00338 (marker)
H00023 Testicular cancer P00338 (marker)
H00035 Ewing's sarcoma P00338 (marker)
H00043 Neuroblastoma P00338 (marker)
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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00770 Congenital myasthenic syndrome P28329 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
C537948 Ceroid lipofuscinosis, neuronal 1, infantile C00007256
D056486 Drug-Induced Liver Injury C00007256
D009336 Necrosis C00007256