class name | count |
---|---|
rosids | 2 |
class name | count |
---|---|
Brassicaceae | 2 |
Enterobacteriaceae | 2 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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 |
---|---|---|---|---|---|---|
C00007230
![]() |
S-Adenosyl-L-homocysteine
|
CHEMBL418052
CHEMBL45041 CHEMBL142828 CHEMBL597532 CHEMBL2092997 |
D012435
|
10 / 7 / 4 | 4 / 2 |
![]() |
C00007347
![]() |
S-Adenosyl-L-methionine
|
CHEMBL224120
CHEMBL1088977 CHEMBL2220241 |
D012436
|
4 / 0 / 0 | 19 / 32 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99873 | Protein arginine N-methyltransferase 1 | Enzyme | C00007230 C00007347 | 0 / 0 |
P50135 | Histamine N-methyltransferase | Enzyme | C00007230 | 0 / 0 |
P49327 | Fatty acid synthase | Transferase | C00007230 | 0 / 0 |
O43463 | Histone-lysine N-methyltransferase SUV39H1 | Enzyme | C00007230 | 0 / 0 |
Q9UBC3 | DNA (cytosine-5)-methyltransferase 3B | Enzyme | C00007230 | 1 / 1 |
P22061 | Protein-L-isoaspartate(D-aspartate) O-methyltransferase | Enzyme | C00007347 | 0 / 0 |
Q8TEK3 | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Enzyme | C00007230 | 0 / 0 |
Q86X55 | Histone-arginine methyltransferase CARM1 | Enzyme | C00007230 | 0 / 0 |
P26358 | DNA (cytosine-5)-methyltransferase 1 | Transferase | C00007230 | 2 / 0 |
O95050 | Indolethylamine N-methyltransferase | Enzyme | C00007230 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00007230 | 4 / 3 |
P11086 | Phenylethanolamine N-methyltransferase | Enzyme | C00007347 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00007347 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1277 | COL1A1, OI4 | collagen, type I, alpha 1 |
C00007230
C00007347
|
1278 | COL1A2, OI4 | collagen, type I, alpha 2 |
C00007230
C00007347
|
1786 | DNMT1, ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT | DNA (cytosine-5-)-methyltransferase 1 (EC:2.1.1.37) |
C00007230
C00007347
|
2099 | ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 | estrogen receptor 1 |
C00007347
|
23743 | BHMT2 | betaine--homocysteine S-methyltransferase 2 (EC:2.1.1.10) |
C00007347
|
836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00007347
|
1312 | COMT | catechol-O-methyltransferase (EC:2.1.1.6) |
C00007347
|
1571 | CYP2E1, CPE1, CYP2E, P450-J, P450C2E | cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) |
C00007347
|
1644 | DDC, AADC | dopa decarboxylase (aromatic L-amino acid decarboxylase) (EC:4.1.1.28) |
C00007347
|
1788 | DNMT3A, DNMT3A2, M.HsaIIIA | DNA (cytosine-5-)-methyltransferase 3 alpha (EC:2.1.1.37) |
C00007347
|
10891 | PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 | peroxisome proliferator-activated receptor gamma, coactivator 1 alpha |
C00007230
|
9687 | GREB1 | growth regulation by estrogen in breast cancer 1 |
C00007347
|
3952 | LEP, LEPD, OB, OBS | leptin |
C00007347
|
5594 | MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk | mitogen-activated protein kinase 1 (EC:2.7.11.24) |
C00007347
|
5595 | MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK | mitogen-activated protein kinase 3 (EC:2.7.11.24) |
C00007347
|
8932 | MBD2, DMTase, NY-CO-41 | methyl-CpG binding domain protein 2 |
C00007347
|
4548 | MTR, HMAG, MS, cblG | 5-methyltetrahydrofolate-homocysteine methyltransferase (EC:2.1.1.13) |
C00007347
|
6667 | SP1 | Sp1 transcription factor |
C00007347
|
7031 | TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 | trefoil factor 1 |
C00007347
|
7040 | TGFB1, CED, DPD1, LAP, TGFB, TGFbeta | transforming growth factor, beta 1 |
C00007347
|
OMIM | preferred title | UniProt |
---|---|---|
#604121 | Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant; adcadn |
P26358
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#242860 | Immunodeficiency-centromeric instability-facial anomalies syndrome 1; icf1 |
Q9UBC3
|
#614116 | Neuropathy, hereditary sensory, type ie; hsn1e |
P26358
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
MESH or OMIM | name |
KNApSAcK
metabolite |
---|---|---|
D001321 | Autistic Disorder |
C00007230
C00007347 |
D007037 | Hypothyroidism |
C00007347
|
D001714 | Bipolar Disorder |
C00007347
|
D002779 | Cholestasis |
C00007347
|
D003072 | Cognition Disorders |
C00007347
|
D003645 | Death, Sudden |
C00007347
|
D003704 | Dementia |
C00007347
|
D003711 | Demyelinating Diseases |
C00007347
|
D003866 | Depressive Disorder |
C00007347
|
D056486 | Drug-Induced Liver Injury |
C00007347
|
D004409 | Dyskinesia, Drug-Induced |
C00007347
|
D005494 | Folic Acid Deficiency |
C00007347
|
D005705 | Gallbladder Diseases |
C00007347
|
D006529 | Hepatomegaly |
C00007347
|
D006948 | Hyperkinesis |
C00007347
|
D018476 | Hypokinesia |
C00007347
|
D009361 | Neoplasm Invasiveness |
C00007230
|
D007565 | Jaundice |
C00007347
|
D008103 | Liver Cirrhosis |
C00007347
|
D008106 | Liver Cirrhosis, Experimental |
C00007347
|
D008107 | Liver Diseases |
C00007347
|
D008113 | Liver Neoplasms |
C00007347
|
D008661 | Metabolism, Inborn Errors |
C00007347
|
D009078 | Mucocele |
C00007347
|
D009127 | Muscle Rigidity |
C00007347
|
D009336 | Necrosis |
C00007347
|
D009410 | Nerve Degeneration |
C00007347
|
D020335 | Paraparesis |
C00007347
|
D051437 | Renal Insufficiency |
C00007347
|
D012559 | Schizophrenia |
C00007347
|
D013118 | Spinal Cord Diseases |
C00007347
|
D014202 | Tremor |
C00007347
|
D014806 | Vitamin B 12 Deficiency |
C00007347
|