class name | count |
---|---|
rosids | 40 |
asterids | 9 |
Spermatophyta | 6 |
Euphyllophyta | 2 |
eudicotyledons | 2 |
Liliopsida | 1 |
class name | count |
---|---|
Fabaceae
![]() |
21 |
Solanaceae
![]() |
5 |
Brassicaceae
![]() |
5 |
Pinaceae
![]() |
5 |
Rosaceae
![]() |
3 |
Hominidae
![]() |
2 |
Fagaceae
![]() |
2 |
Euphorbiaceae
![]() |
2 |
Rutaceae
![]() |
2 |
Poaceae
![]() |
1 |
Anacardiaceae
![]() |
1 |
Saccharomycetaceae
![]() |
1 |
Vitaceae
![]() |
1 |
Ebenaceae
![]() |
1 |
Rhizopodaceae
![]() |
1 |
Betulaceae
![]() |
1 |
Cupressaceae
![]() |
1 |
Lygodiaceae
![]() |
1 |
Araliaceae
![]() |
1 |
Cucurbitaceae
![]() |
1 |
br08003 Category | # of metabolite |
---|---|
Indole alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Indole alkaloids | C00954 | C00000100 |
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
![]() |
IAA
/ Indole-3-acetic acid |
CHEMBL82411
|
C030737
|
3 / 0 / 0 | 2 / 1 |
![]() |
C00000115
![]() |
Indol-3-propionic acid
/ 1H-Indole-3-propanoic acid |
CHEMBL207225
|
C015292
|
1 / 0 / 0 |
![]() |
|
C00000116
![]() |
IBA
/ Indole-3-butyric acid / 1H-Indole-3-butanoic acid |
CHEMBL582878
|
C014612
|
6 / 9 / 8 |
![]() |
|
C00001331
![]() |
L-Abrine
|
CHEMBL552941
CHEMBL2360657 |
2 / 0 / 0 |
![]() |
||
C00001396
![]() |
L-Tryptophan
|
CHEMBL54976
CHEMBL292303 CHEMBL484901 |
49 / 41 / 39 |
![]() |
||
C00001740
![]() |
Hypaphorine
|
CHEMBL503867
CHEMBL448328 |
C001529
|
3 / 1 / 1 |
![]() |
|
C00007571
![]() |
IPA
/ Indolepyruvate |
CHEMBL485012
|
16 / 20 / 16 |
![]() |
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 |
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
|
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 | 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)
|