KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (6)

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
C00001496 External link 512 Crotonoside
CHEMBL296017
CHEMBL609077
CHEMBL1688963
CHEMBL1741830
C008184
10 / 2 / 3
C00018365 External link 512 Oxanosine
/ NSC 359452
CHEMBL1969011
C032886
C00018670 External link 512 U 10071
/ Tubercidine
/ Sparsamycin A
/ 7-Deazaadenosine
/ Antibiotic XK 101-1
CHEMBL267099
CHEMBL599189
CHEMBL2093914
CHEMBL2311082
D014372
12 / 13 / 5
C00018685 External link 512 Nebularine
/ Purinosine
/ Ribosylpurine
/ Purine riboside
/ Purine-9-beta-D-ribofuranoside
/ 9-beta-D-Ribofuranosyl-9H-purine
CHEMBL1399702
CHEMBL1476759
C005248
15 / 30 / 55
C00019679 External link 512 Guanosine
/ 9-beta-D-Ribofuranosylguanine
CHEMBL278434
CHEMBL375655
CHEMBL240933
CHEMBL607672
CHEMBL2021379
CHEMBL2093064
D006151
5 / 4 / 4 3 / 0
C00019692 External link 512 Inosine
CHEMBL9850
CHEMBL1556
CHEMBL1213651
CHEMBL2092757
D007288
13 / 14 / 5 2 / 2

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001496 C00018685 1 / 0
P23526 Adenosylhomocysteinase Enzyme C00019679 C00019692 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00018670 C00019692 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00018685 C00019692 4 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018670 C00019692 0 / 0
Q99700 Ataxin-2 Unclassified protein C00018670 C00019692 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00001496 C00018670 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001496 C00018685 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001496 C00018685 1 / 1
P00491 Purine nucleoside phosphorylase Enzyme C00018670 C00019692 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001496 C00018685 0 / 0
O75496 Geminin Unclassified protein C00018670 C00019692 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001496 C00018685 0 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018670 C00019692 2 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00018670 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00019692 0 / 0
P68871 Hemoglobin subunit beta Secreted protein C00018685 4 / 4
P54132 Bloom syndrome protein Enzyme C00018685 1 / 2
P04183 Thymidine kinase, cytosolic Enzyme C00019679 0 / 1
P35348 Alpha-1A adrenergic receptor Adrenergic receptor C00018685 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00019692 1 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00018670 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00018670 0 / 0
P55263 Adenosine kinase Enzyme C00018670 1 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00019692 3 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00018685 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00018685 0 / 0
P00813 Adenosine deaminase Hydrolase C00018685 1 / 1
P02545 Prelamin-A/C Unclassified protein C00018685 11 / 10
O15245 Solute carrier family 22 member 1 Drug uniporter C00019692 0 / 0
O00142 Thymidine kinase 2, mitochondrial Enzyme C00019679 1 / 1
P00492 Hypoxanthine-guanine phosphoribosyltransferase Enzyme C00019679 2 / 1
Q6DHV7 Adenosine deaminase-like protein Enzyme C00001496 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00019692 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00019679 0 / 0
Q53EL6 Programmed cell death protein 4 Unclassified protein C00018670 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00018685 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00018685 7 / 37
P29274 Adenosine receptor A2a Adenosine receptor C00001496 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00001496 0 / 0
P29275 Adenosine receptor A2b Adenosine receptor C00001496 0 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00019679
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) C00019679
55315 SLC29A3, ENT3, HCLAP, HJCD, PHID solute carrier family 29 (equilibrative nucleoside transporter), member 3 C00019679
100 ADA adenosine deaminase (EC:3.5.4.4) C00019692
356 FASLG, ALPS1B, APT1LG1, APTL, CD178, CD95-L, CD95L, FASL, TNFSF6 Fas ligand (TNF superfamily, member 6) C00019692

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (51)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#613985 Beta-thalassemia P68871
#603902 Beta-thalassemia, dominant inclusion body type P68871
#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
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#140700 Heinz body anemias P68871
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#614300 Hypermethioninemia due to adenosine kinase deficiency P55263
#613752 Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency P23526
#300323 Kelley-seegmiller syndrome P00492
#300322 Lesch-nyhan syndrome; lns P00492
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#609560 Mitochondrial dna depletion syndrome 2 (myopathic type); mtdps2 O00142
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#613179 Purine nucleoside phosphorylase deficiency P00491
#275210 Restrictive dermopathy, lethal P02545
#102700 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency P00813
#603903 Sickle cell anemia P68871
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828

KEGG DISEASE (64)

KEGG name UniProt
H00469 Mitochondrial DNA depletion syndrome (MDS) O00142 (related)
H00093 Combined immunodeficiencies (CIDs) P00491 (related)
H00194 Lesch-Nyhan syndrome P00492 (related)
H00092 T-B-Severe combined immunodeficiencies (SCIDs) P00813 (related)
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)
H00005 Chronic lymphocytic leukemia (CLL) P04183 (marker)
P04637 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
P68871 (marker)
H00022 Bladder cancer P04637 (related)
P68871 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H00184 Hypermethioninemia P23526 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00228 Thalassemia P68871 (related)
H00229 Sickle cell anemia (SCA) P68871 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009202 Cardiomyopathies C00019692
D007970 Leukopenia C00019692