| 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
|
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)
|