Plant Species


Cumulative plant class count

class name count
rosids 2

Cumulative family count

class name count
Brassicaceae 2
Enterobacteriaceae 2

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (2)

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 External link 512 S-Adenosyl-L-homocysteine
CHEMBL418052
CHEMBL45041
CHEMBL142828
CHEMBL597532
CHEMBL2092997
D012435
10 / 7 / 4 4 / 2
C00007347 External link 512 S-Adenosyl-L-methionine
CHEMBL224120
CHEMBL1088977
CHEMBL2220241
D012436
4 / 0 / 0 19 / 32

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

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

20 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

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

KEGG DISEASE (4)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00087 Other humoral immunodeficiencies Q9UBC3 (related)

Diseases related to CTD interactions

33 disease in interactions with metabolites

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