KCF-S cluster No. 1432 (7 metabolites)

Corresponding Phytochemical cluster No. 4



Metabolite list (7)

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
C00000100 External link 512 IAA
/ Indole-3-acetic acid
CHEMBL82411
C030737
3 / 0 / 0 2 / 1
C00000115 External link 512 Indol-3-propionic acid
/ 1H-Indole-3-propanoic acid
CHEMBL207225
C015292
1 / 0 / 0
C00000116 External link 512 IBA
/ Indole-3-butyric acid
/ 1H-Indole-3-butanoic acid
CHEMBL582878
C014612
6 / 9 / 8
C00001331 External link 512 L-Abrine
CHEMBL552941
CHEMBL2360657
2 / 0 / 0
C00001396 External link 512 L-Tryptophan
CHEMBL54976
CHEMBL292303
CHEMBL484901
49 / 41 / 39
C00001740 External link 512 Hypaphorine
CHEMBL503867
CHEMBL448328
C001529
3 / 1 / 1
C00007571 External link 512 IPA
/ Indolepyruvate
CHEMBL485012
16 / 20 / 16

Human Protein / Gene in interactions

65 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16773 Kynurenine--oxoglutarate transaminase 1 Enzyme C00000100 C00000115 C00001396 C00007571 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001331 C00001396 C00007571 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001396 C00001740 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001396 C00007571 0 / 0
Q05BR4 SLC16A10 protein Unclassified protein C00001331 C00001396 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001396 C00007571 4 / 3
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001396 C00007571 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001396 C00007571 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001396 C00007571 1 / 2
O75496 Geminin Unclassified protein C00001396 C00007571 0 / 0
O00255 Menin Unclassified protein C00001396 C00007571 2 / 5
P02768 Serum albumin Secreted protein C00000100 C00001396 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001396 0 / 1
P02545 Prelamin-A/C Unclassified protein C00001396 11 / 10
Q9Y263 Phospholipase A-2-activating protein Unclassified protein C00001396 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00001396 3 / 2
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00000116 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00001396 1 / 2
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00000116 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001396 0 / 1
P54132 Bloom syndrome protein Enzyme C00001396 1 / 2
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00001396 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00001396 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00001396 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00007571 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00001396 1 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001396 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001396 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001396 0 / 0
P42858 Huntingtin Unclassified protein C00001396 1 / 1
P43166 Carbonic anhydrase 7 Lyase C00001396 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00001396 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00007571 7 / 3
P09923 Intestinal-type alkaline phosphatase Enzyme C00001396 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00001396 3 / 1
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00001396 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00007571 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00000116 5 / 3
Q9HBH1 Peptide deformylase, mitochondrial Enzyme C00000100 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001396 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00001396 0 / 1
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00001396 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00007571 2 / 2
Q01453 Peripheral myelin protein 22 Unclassified protein C00001396 5 / 2
P03372 Estrogen receptor NR3A1 C00000116 1 / 1
P48775 Tryptophan 2,3-dioxygenase Enzyme C00001396 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00001396 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001396 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00007571 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00001396 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00007571 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00001740 1 / 1
P06746 DNA polymerase beta Enzyme C00001740 0 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00001396 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000116 0 / 0
P10275 Androgen receptor NR3C4 C00000116 3 / 4
P07451 Carbonic anhydrase 3 Lyase C00001396 0 / 0
P08254 Stromelysin-1 M10A C00001396 1 / 0
P22748 Carbonic anhydrase 4 Lyase C00001396 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001396 2 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001396 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00007571 4 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00001396 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001396 1 / 4
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001396 1 / 0

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000100
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00000100

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (64)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#232300 Glycogen storage disease ii P10253
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (53)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
H00026 Endometrial Cancer P03372 (marker)
H00213 Hypophosphatasia P05186 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00059 Huntington's disease (HD) P42858 (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)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00208 Hyperbilirubinemia Q92887 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00000100