class name | count |
---|---|
asterids | 42 |
rosids | 42 |
eudicotyledons | 9 |
Spermatophyta | 7 |
Magnoliophyta | 2 |
class name | count |
---|---|
Acanthaceae | 35 |
Rutaceae | 22 |
Phyllanthaceae | 13 |
Berberidaceae | 9 |
Cupressaceae | 7 |
Polygalaceae | 2 |
Araliaceae | 2 |
Apiaceae | 2 |
Asteraceae | 2 |
Salicaceae | 1 |
Hernandiaceae | 1 |
Lamiaceae | 1 |
Fabaceae | 1 |
Lauraceae | 1 |
Linaceae | 1 |
Clusiaceae | 1 |
Burseraceae | 1 |
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 |
---|---|---|---|---|---|---|
C00000611
![]() |
Justicidin E
|
CHEMBL304236
|
1 / 0 / 0 |
![]() |
||
C00000700
![]() |
Justicidin A
|
CHEMBL508532
|
C049719
|
![]() |
||
C00000701
![]() |
Justicidin B
|
![]() |
||||
C00000711
![]() |
Retrojusticidin B
|
CHEMBL292540
|
1 / 0 / 0 |
![]() |
||
C00000720
![]() |
Neojusticin A
|
CHEMBL455369
|
![]() |
|||
C00000721
![]() |
Taiwanin E
|
CHEMBL468453
|
![]() |
|||
C00000727
![]() |
Prostalidin A
|
![]() |
||||
C00000728
![]() |
Prostalidin B
|
![]() |
||||
C00000729
![]() |
Prostalidin C
|
![]() |
||||
C00002600
![]() |
Diphyllin
|
CHEMBL221190
|
C010130
|
24 / 43 / 38 |
![]() |
|
C00007210
![]() |
Dehydropodophyllotoxin
/ Tetradehydropodophyllotoxin |
CHEMBL487214
|
![]() |
|||
C00007211
![]() |
Helioxanthin
|
CHEMBL436474
|
![]() |
|||
C00030455
![]() |
Haplomyrtin
|
![]() |
||||
C00031016
![]() |
Phyllanthusmin A
|
![]() |
||||
C00031681
![]() |
Cleistanone
/ (+)-Cleistanone |
![]() |
||||
C00036091
![]() |
Chaihunaphthone
|
![]() |
||||
C00036092
![]() |
Chinensinaphthol
|
CHEMBL495476
|
![]() |
|||
C00037881
![]() |
Taiwanin C
|
CHEMBL65755
|
1 / 0 / 0 |
![]() |
||
C00049571
![]() |
Cilinaphthalide A
|
CHEMBL491523
|
![]() |
|||
C00049572
![]() |
Cilinaphthalide B
|
CHEMBL521623
|
![]() |
|||
C00049574
![]() |
Chinensinaphthol methyl ether
|
CHEMBL510411
|
![]() |
|||
C00049575
![]() |
Neojusticin B
|
CHEMBL455623
|
![]() |
|||
C00049576
![]() |
Taiwanin E methyl ether
|
CHEMBL495475
|
![]() |
|||
C00049959
![]() |
5-Methoxyjusticidin A
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00000611 C00000711 C00037881 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002600 | 0 / 0 |
Q9Y5X4 | Photoreceptor-specific nuclear receptor | NR2E3 | C00002600 | 2 / 2 |
P02545 | Prelamin-A/C | Unclassified protein | C00002600 | 11 / 10 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00002600 | 0 / 0 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002600 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002600 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002600 | 2 / 2 |
P42858 | Huntingtin | Unclassified protein | C00002600 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002600 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00002600 | 0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00002600 | 4 / 2 |
Q99700 | Ataxin-2 | Unclassified protein | C00002600 | 1 / 1 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002600 | 7 / 3 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00002600 | 2 / 2 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002600 | 2 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002600 | 0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00002600 | 1 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002600 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002600 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002600 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002600 | 1 / 0 |
O00255 | Menin | Unclassified protein | C00002600 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002600 | 1 / 2 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00002600 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#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
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#268100 | Enhanced s-cone syndrome; escs |
Q9Y5X4
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#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
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#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
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#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
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#611131 | Retinitis pigmentosa 37; rp37 |
Q9Y5X4
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#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)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00027 | Ovarian cancer |
P38398
(related)
|
H00031 | Breast cancer |
P38398
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(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) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00527 | Retinitis pigmentosa (RP) |
Q9Y5X4
(related)
|
H00805 | Vitreoretinal degeneration |
Q9Y5X4
(related)
|