class name | count |
---|---|
rosids | 3 |
class name | count |
---|---|
Enterobacteriaceae | 4 |
Brassicaceae | 3 |
br08003 Category | # of metabolite |
---|---|
Pyridine alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Pyridine alkaloids | C13051 | C00007537 |
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
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NAD
/ Nicotinamide adenine dinucleotide |
CHEMBL234870
CHEMBL1234613 CHEMBL1402028 CHEMBL1454168 CHEMBL1517480 |
D009243
|
18 / 25 / 24 | 23 / 3 |
![]() |
C00007537
![]() |
Nicotinic acid adenine dinucleotide
|
C024376
|
1 / 0 |
![]() |
||
C00007538
![]() |
2'-O-Acetyl-ADP-ribose
|
![]() |
||||
C00019343
![]() |
NADH
/ Dihydronicotinamide adenine dinucleotide |
CHEMBL1161866
|
2 / 0 / 0 |
![]() |
||
C00019545
![]() |
TPNH
/ NADPH |
CHEMBL407009
CHEMBL1594246 CHEMBL1619387 CHEMBL1623059 |
7 / 3 / 1 |
![]() |
||
C00019568
![]() |
Nicotinic acid dinucleotide
|
C018348
|
1 / 0 |
![]() |
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 |
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
|
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 | 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)
|