class name | count |
---|---|
rosids | 2 |
Liliopsida | 2 |
eudicotyledons | 1 |
class name | count |
---|---|
Streptomycetaceae | 3 |
Enterobacteriaceae | 2 |
Phyllanthaceae | 1 |
Hymenochaetaceae | 1 |
Euphorbiaceae | 1 |
Agaricaceae | 1 |
Crassulaceae | 1 |
Subergorgiidae | 1 |
Poaceae | 1 |
Amaryllidaceae | 1 |
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 |
---|---|---|---|---|---|---|
C00001496
![]() |
Crotonoside
|
CHEMBL296017
CHEMBL609077 CHEMBL1688963 CHEMBL1741830 |
C008184
|
10 / 2 / 3 |
![]() |
|
C00018365
![]() |
Oxanosine
/ NSC 359452 |
CHEMBL1969011
|
C032886
|
![]() |
||
C00018670
![]() |
U 10071
/ Tubercidine / Sparsamycin A / 7-Deazaadenosine / Antibiotic XK 101-1 |
CHEMBL267099
CHEMBL599189 CHEMBL2093914 CHEMBL2311082 |
D014372
|
12 / 13 / 5 |
![]() |
|
C00018685
![]() |
Nebularine
/ Purinosine / Ribosylpurine / Purine riboside / Purine-9-beta-D-ribofuranoside / 9-beta-D-Ribofuranosyl-9H-purine |
CHEMBL1399702
CHEMBL1476759 |
C005248
|
15 / 30 / 55 |
![]() |
|
C00019679
![]() |
Guanosine
/ 9-beta-D-Ribofuranosylguanine |
CHEMBL278434
CHEMBL375655 CHEMBL240933 CHEMBL607672 CHEMBL2021379 CHEMBL2093064 |
D006151
|
5 / 4 / 4 | 3 / 0 |
![]() |
C00019692
![]() |
Inosine
|
CHEMBL9850
CHEMBL1556 CHEMBL1213651 CHEMBL2092757 |
D007288
|
13 / 14 / 5 | 2 / 2 |
![]() |
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 |
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
|
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 | 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)
|