class name | count |
---|---|
asterids | 9 |
eudicotyledons | 4 |
rosids | 2 |
Liliopsida | 1 |
class name | count |
---|---|
Rubiaceae | 7 |
Polygonaceae | 4 |
Fabaceae | 2 |
Xanthorrhoeaceae | 1 |
Asteraceae | 1 |
Scrophulariaceae | 1 |
Aspergillaceae | 1 |
Phaeosphaeriaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Anthraquinone type | 2 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Anthraquinone type | C10394 | C00002856 |
Anthraquinone type | C10401 | C00002861 |
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 |
---|---|---|---|---|---|---|
C00002856
![]() |
Pseudopurpurin
|
![]() |
||||
C00002861
![]() |
Rhein
|
CHEMBL418068
|
C020491
|
60 / 65 / 46 | 8 / 1 |
![]() |
C00016317
![]() |
NSC 624610
/ Emodic acid / 9,10-Dihydro-4,5,7-trihydroxy-9,10-dioxo-2-anthroic acid |
CHEMBL290914
|
32 / 18 / 20 |
![]() |
||
C00018257
![]() |
Endocrocin
|
C023523
|
![]() |
|||
C00032095
![]() |
Ophiohayatone C
|
![]() |
||||
C00033228
![]() |
Munjistin
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00002861 C00016317 | 2 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002861 C00016317 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002861 C00016317 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002861 C00016317 | 1 / 2 |
O00255 | Menin | Unclassified protein | C00002861 C00016317 | 2 / 5 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002861 C00016317 | 1 / 1 |
P08246 | Neutrophil elastase | S1A | C00002861 C00016317 | 2 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00002861 C00016317 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00002861 C00016317 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002861 C00016317 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002861 C00016317 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002861 C00016317 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002861 C00016317 | 4 / 3 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002861 C00016317 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002861 C00016317 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002861 C00016317 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002861 C00016317 | 1 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002861 C00016317 | 0 / 1 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002861 C00016317 | 2 / 2 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002861 C00016317 | 1 / 1 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002861 C00016317 | 0 / 0 |
P08311 | Cathepsin G | S1A | C00002861 C00016317 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00002861 C00016317 | 0 / 0 |
P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00002861 | 5 / 3 |
O75496 | Geminin | Unclassified protein | C00002861 | 0 / 0 |
P10145 | Interleukin-8 | Secreted protein | C00002861 | 0 / 0 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00002861 | 0 / 0 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002861 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00016317 | 0 / 0 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00002861 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002861 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00016317 | 0 / 0 |
Q99816 | Tumor susceptibility gene 101 protein | Unclassified protein | C00002861 | 0 / 0 |
P04150 | Glucocorticoid receptor | NR3C1 | C00002861 | 0 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002861 | 2 / 0 |
P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00002861 | 2 / 0 |
Q96RI1 | Bile acid receptor | NR1H4 | C00002861 | 0 / 0 |
P35236 | Tyrosine-protein phosphatase non-receptor type 7 | Tyr | C00002861 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00016317 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002861 | 3 / 3 |
Q15149 | Plectin | Unclassified protein | C00002861 | 4 / 3 |
Q9Y3R4 | Sialidase-2 | Enzyme | C00002861 | 0 / 0 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00002861 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00002861 | 1 / 1 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002861 | 0 / 0 |
P55210 | Caspase-7 | C14 | C00002861 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00002861 | 2 / 3 |
P54132 | Bloom syndrome protein | Enzyme | C00002861 | 1 / 2 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002861 | 3 / 1 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00002861 | 3 / 2 |
P02545 | Prelamin-A/C | Unclassified protein | C00002861 | 11 / 10 |
Q13547 | Histone deacetylase 1 | Hydrolase | C00016317 | 0 / 0 |
Q03181 | Peroxisome proliferator-activated receptor delta | NR1C2 | C00002861 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002861 | 0 / 0 |
P29466 | Caspase-1 | C14 | C00002861 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002861 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00016317 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002861 | 1 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00002861 | 2 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00016317 | 1 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00016317 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00016317 | 1 / 4 |
Q92731 | Estrogen receptor beta | NR3A2 | C00002861 | 0 / 1 |
P07900 | Heat shock protein HSP 90-alpha | Other cytosolic protein | C00002861 | 0 / 0 |
P08238 | Heat shock protein HSP 90-beta | Other cytosolic protein | C00002861 | 0 / 0 |
P09619 | Platelet-derived growth factor receptor beta | Pdgfr | C00002861 | 5 / 1 |
P16234 | Platelet-derived growth factor receptor alpha | Pdgfr | C00002861 | 2 / 1 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00002861 | 4 / 1 |
Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00016317 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
196 | AHR, bHLHe76 | aryl hydrocarbon receptor |
C00002861
|
1950 | EGF, HOMG4, URG | epidermal growth factor |
C00002861
|
2064 | ERBB2, CD340, HER-2, HER-2/neu, HER2, MLN_19, NEU, NGL, TKR1 | v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 (EC:2.7.10.1) |
C00002861
|
3091 | HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 | hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) |
C00002861
|
4790 | NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 | nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 |
C00002861
|
5743 | PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 | prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) |
C00002861
|
5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A |
C00002861
|
7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A |
C00002861
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#615007 | Basal ganglia calcification, idiopathic, 4; ibgc4 |
P09619
|
#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
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P18054
P84022 Q14191 |
#162800 | Cyclic neutropenia |
P08246
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#226670 | Epidermolysis bullosa simplex with muscular dystrophy |
Q15149
|
#612138 | Epidermolysis bullosa simplex with pyloric atresia |
Q15149
|
#131950 | Epidermolysis bullosa simplex, ogna type |
Q15149
|
#133239 | Esophageal cancer |
P18054
|
#615363 | Estrogen resistance; estrr |
P03372
|
#612219 | Ewing sarcoma; es |
P11308
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#606764 | Gastrointestinal stromal tumor; gist |
P16234
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
P37231 |
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#607685 | Hypereosinophilic syndrome, idiopathic; hes |
P16234
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#607785 | Juvenile myelomonocytic leukemia; jmml |
P09619
|
#601626 | Leukemia, acute myeloid; aml |
P09619
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#613723 | Muscular dystrophy, limb-girdle, type 2q; lgmd2q |
Q15149
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#131440 | Myeloproliferative disorder, chronic, with eosinophilia |
P09619
|
#228550 | Myofibromatosis, infantile, 1; imf1 |
P09619
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#202700 | Neutropenia, severe congenital, 1, autosomal dominant; scn1 |
P08246
|
#601665 | Obesity |
P37231
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#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
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#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
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(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)
Q15149 (related) |
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
Q15149 (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)
Q92731 (marker) |
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00100 | Neutropenic disorders |
P08246
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00042 | Glioma |
P09619
(related)
P16234 (related) |
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(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)
|
H00032 | Thyroid cancer |
P37231
(related)
|
H00409 | Type II diabetes mellitus |
P37231
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (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)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00585 | Epidermolysis bullosa, hemidesmosomal |
Q15149
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|