Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Methanobacteriaceae 2
Methanosarcinaceae 2
Axinellidae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (3)

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
C00000761 External link 512 Coenzyme M
CHEMBL1098319
C00000762 External link 512 S-Methyl coenzyme M
C00048188 External link 512 Taurine
CHEMBL239243
D013654
14 / 21 / 19 55 / 38

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00048188 1 / 0
P04062 Glucosylceramidase Enzyme C00048188 6 / 4
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00048188 0 / 0
P02545 Prelamin-A/C Unclassified protein C00048188 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00048188 0 / 1
P54132 Bloom syndrome protein Enzyme C00048188 1 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00048188 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00048188 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00048188 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00048188 0 / 0
Q7Z2H8 Proton-coupled amino acid transporter 1 Unclassified protein C00048188 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00048188 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00048188 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00048188 1 / 0

55 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
27 ABL2, ABLL, ARG c-abl oncogene 2, non-receptor tyrosine kinase (EC:2.7.10.2) C00048188
55803 ADAP2, CENTA2, HSA272195, cent-b ArfGAP with dual PH domains 2 C00048188
135 ADORA2A, A2aR, ADORA2, RDC8 adenosine A2a receptor C00048188
147 ADRA1B, ADRA1, ALPHA1BAR adrenoceptor alpha 1B C00048188
637 BID, FP497 BH3 interacting domain death agonist C00048188
659 BMPR2, BMPR-II, BMPR3, BMR2, BRK-3, PPH1, T-ALK bone morphogenetic protein receptor, type II (serine/threonine kinase) (EC:2.7.11.30) C00048188
10486 CAP2 CAP, adenylate cyclase-associated protein, 2 (yeast) C00048188
1081 CGA, CG-ALPHA, FSHA, GPHA1, GPHa, HCG, LHA, TSHA glycoprotein hormones, alpha polypeptide C00048188
1123 CHN1, ARHGAP2, CHN, DURS2, NC, RHOGAP2 chimerin 1 C00048188
9318 COPS2, ALIEN, CSN2, SGN2, TRIP15 COP9 signalosome subunit 2 C00048188
2833 CXCR3, CD182, CD183, CKR-L2, CMKAR3, GPR9, IP10-R, Mig-R, MigR chemokine (C-X-C motif) receptor 3 C00048188
23576 DDAH1, DDAH dimethylarginine dimethylaminohydrolase 1 (EC:3.5.3.18) C00048188
8525 DGKZ, DAGK5, DAGK6, DGK-ZETA, hDGKzeta diacylglycerol kinase, zeta (EC:2.7.1.107) C00048188
9538 EI24, EPG4, PIG8, TP53I8 etoposide induced 2.4 C00048188
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00048188
2260 FGFR1, BFGFR, CD331, CEK, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 fibroblast growth factor receptor 1 (EC:2.7.10.1) C00048188
2741 GLRA1, HKPX1, STHE glycine receptor, alpha 1 C00048188
2917 GRM7, GLUR7, GPRC1G, MGLU7, MGLUR7 glutamate receptor, metabotropic 7 C00048188
2982 GUCY1A3, GC-SA3, GUC1A3, GUCA3, GUCSA3, GUCY1A1 guanylate cyclase 1, soluble, alpha 3 (EC:4.6.1.2) C00048188
3146 HMGB1, HMG1, HMG3, SBP-1 high mobility group box 1 C00048188
3486 IGFBP3, BP-53, IBP3 insulin-like growth factor binding protein 3 C00048188
889 KRIT1, CAM, CCM1 KRIT1, ankyrin repeat containing C00048188
10314 LANCL1, GPR69A, p40 LanC lantibiotic synthetase component C-like 1 (bacterial) C00048188
4067 LYN, JTK8, p53Lyn, p56Lyn v-yes-1 Yamaguchi sarcoma viral related oncogene homolog (EC:2.7.10.2) C00048188
64231 MS4A6A, 4SPAN3, 4SPAN3.2, CD20L3, MS4A6, MST090, MSTP090 membrane-spanning 4-domains, subfamily A, member 6A C00048188
81285 OR51E2, OR51E3P, OR52A2, PSGR olfactory receptor, family 51, subfamily E, member 2 C00048188
55824 PAG1, CBP, PAG phosphoprotein associated with glycosphingolipid microdomains 1 C00048188
10298 PAK4 p21 protein (Cdc42/Rac)-activated kinase 4 (EC:2.7.11.1) C00048188
5423 POLB polymerase (DNA directed), beta (EC:2.7.7.7) C00048188
5424 POLD1, CDC2, CRCS10, MDPL, POLD polymerase (DNA directed), delta 1, catalytic subunit (EC:2.7.7.7) C00048188
27434 POLM, Pol_Mu, Tdt-N polymerase (DNA directed), mu (EC:2.7.7.7) C00048188
26051 PPP1R16B, ANKRD4, TIMAP protein phosphatase 1, regulatory subunit 16B C00048188
5529 PPP2R5E protein phosphatase 2, regulatory subunit B', epsilon isoform C00048188
5577 PRKAR2B, PRKAR2, RII-BETA protein kinase, cAMP-dependent, regulatory, type II, beta (EC:2.7.11.1) C00048188
5664 PSEN2, AD3L, AD4, CMD1V, PS2, STM2 presenilin 2 (Alzheimer disease 4) C00048188
5796 PTPRK, R-PTP-kappa protein tyrosine phosphatase, receptor type, K (EC:3.1.3.48) C00048188
5868 RAB5A, RAB5 RAB5A, member RAS oncogene family C00048188
5889 RAD51C, BROVCA3, FANCO, R51H3, RAD51L2 RAD51 paralog C C00048188
5883 RAD9A, RAD9 RAD9 homolog A (S. pombe) (EC:3.1.11.2) C00048188
9693 RAPGEF2, CNrasGEF, NRAPGEP, PDZ-GEF1, PDZGEF1, RA-GEF, RA-GEF-1, Rap-GEP, nRap_GEP Rap guanine nucleotide exchange factor (GEF) 2 C00048188
10125 RASGRP1, CALDAG-GEFI, CALDAG-GEFII, RASGRP, V, hRasGRP1 RAS guanyl releasing protein 1 (calcium and DAG-regulated) C00048188
6196 RPS6KA2, HU-2, MAPKAPK1C, RSK, RSK3, S6K-alpha, S6K-alpha2, p90-RSK3, pp90RSK3 ribosomal protein S6 kinase, 90kDa, polypeptide 2 (EC:2.7.11.1) C00048188
6447 SCG5, 7B2, P7B2, SGNE1, SgV secretogranin V (7B2 protein) C00048188
9126 SMC3, BAM, BMH, CDLS3, CSPG6, HCAP, SMC3L1 structural maintenance of chromosomes 3 C00048188
10302 SNAPC5, SNAP19 small nuclear RNA activating complex, polypeptide 5, 19kDa C00048188
10253 SPRY2, hSPRY2 sprouty homolog 2 (Drosophila) C00048188
6729 SRP54 signal recognition particle 54kDa C00048188
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00048188
6869 TACR1, NK1R, NKIR, SPR, TAC1R tachykinin receptor 1 C00048188
7010 TEK, CD202B, TIE-2, TIE2, VMCM, VMCM1 TEK tyrosine kinase, endothelial (EC:2.7.10.1) C00048188
7040 TGFB1, CED, DPD1, LAP, TGFB, TGFbeta transforming growth factor, beta 1 C00048188
9540 TP53I3, PIG3 tumor protein p53 inducible protein 3 C00048188
7297 TYK2, JTK1 tyrosine kinase 2 (EC:2.7.10.2) C00048188
7415 VCP, ALS14, IBMPFD, IBMPFD1, TERA, p97 valosin containing protein (EC:3.6.4.6) C00048188
7518 XRCC4 X-ray repair complementing defective repair in Chinese hamster cells 4 C00048188

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (21)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#137800 Glioma susceptibility 1; glm1 O75874
#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
#168600 Parkinson disease, late-onset; pd P04062
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (19)

KEGG name UniProt
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)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)

Diseases related to CTD interactions

38 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D055371 Acute Lung Injury C00048188
D000860 Anoxia C00048188
D001145 Arrhythmias, Cardiac C00048188
D001919 Bradycardia C00048188
D009202 Cardiomyopathies C00048188
D003329 Coronary Vasospasm C00048188
D003921 Diabetes Mellitus, Experimental C00048188
D003922 Diabetes Mellitus, Type 1 C00048188
D058065 Diabetic Cardiomyopathies C00048188
D003928 Diabetic Nephropathies C00048188
D056486 Drug-Induced Liver Injury C00048188
D050171 Dyslipidemias C00048188
D004487 Edema C00048188
D019446 Endotoxemia C00048188
D005198 Fanconi Syndrome C00048188
D005355 Fibrosis C00048188
D005923 Glomerulosclerosis, Focal Segmental C00048188
D006323 Heart Arrest C00048188
D006331 Heart Diseases C00048188
D006470 Hemorrhage C00048188
D006943 Hyperglycemia C00048188
D017495 Hyperpigmentation C00048188
D006973 Hypertension C00048188
D006984 Hypertrophy C00048188
D007022 Hypotension C00048188
D007249 Inflammation C00048188
D007674 Kidney Diseases C00048188
D007859 Learning Disorders C00048188
D008106 Liver Cirrhosis, Experimental C00048188
D009069 Movement Disorders C00048188
D009133 Muscular Atrophy C00048188
D009203 Myocardial Infarction C00048188
D009336 Necrosis C00048188
D009845 Oligospermia C00048188
D011014 Pneumonia C00048188
D011507 Proteinuria C00048188
D012640 Seizures C00048188
D013733 Testicular Diseases C00048188