Organism name | Physalis peruviana |
---|---|
Genus | Physalis |
Family | Solanaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Physalis peruviana |
---|---|
Linked NCBI taxonomy ID | 126903 |
Linked level | species |
Family in NCBI taxonomy | Solanaceae |
---|---|
ID | 4070 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00005401
![]() |
Quercetin 3-robinoside
/ Quercetin 3-O-robinoside / Quercetin 3-O-robinobioside / Quercetin 3-O-rhamnosyl-(1->6)-galactoside |
CHEMBL32579
CHEMBL310754 CHEMBL182108 CHEMBL226335 CHEMBL502782 CHEMBL1436093 CHEMBL1532989 |
25 / 18 / 16 | No. 1 | No. 15 |
![]() |
||
C00005169
![]() |
Nicotiflorin
/ Nicotifloroside / Kaempferol 3-O-rutinoside / Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside / (-)-Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside |
CHEMBL431610
CHEMBL79790 CHEMBL255020 CHEMBL501550 CHEMBL498879 CHEMBL1419228 CHEMBL1875691 |
22 / 10 / 12 | No. 1 | No. 15 |
![]() |
||
C00005160
![]() |
Kaempferol 3-robinobioside
|
CHEMBL431610
CHEMBL79790 CHEMBL255020 CHEMBL501550 CHEMBL498879 CHEMBL1419228 CHEMBL1875691 |
22 / 10 / 12 | No. 1 | No. 15 |
![]() |
||
C00005239
![]() |
Kaempferol 3-rutinoside-7-glucoside
|
No. 5 | No. 15 |
![]() |
||||
C00005460
![]() |
Quercetin 3-robinobioside-7-glucoside
|
No. 5 | No. 15 |
![]() |
||||
C00005225
![]() |
Kaempferol 3-robinobioside-7-glucoside
|
No. 5 | No. 15 |
![]() |
||||
C00039032
![]() |
Dihydrowithanolide E
/ 2,3-Dihydrowithanolide E |
No. 176 | No. 58 |
![]() |
||||
C00040752
![]() |
(20S,22R)-5beta,6beta-Epoxy-4beta,14beta,15alpha-trihydroxy-1-oxowith-2,24-dienolide
/ (+)-(20S,22R)-5beta,6beta-Epoxy-4beta,14beta,15alpha-trihydroxy-1-oxowith-2,24-dienolide |
No. 176 | No. 58 |
![]() |
||||
C00041219
![]() |
Withaphysanolide
|
No. 729 |
![]() |
|||||
C00025557
![]() |
Tigloidin
/ Tigloyl pseudotropine / 3beta-Tigloyloxytropane |
CHEMBL2107120
CHEMBL2107196 |
No. 1464 | No. 1 |
![]() |
|||
C00002304
![]() |
Tigloidine
|
CHEMBL2107120
CHEMBL2107196 |
No. 1464 | No. 1 |
![]() |
|||
C00037123
![]() |
Ethyl 3-hydroxyoctanoate 3-O-beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranoside
|
No. 2396 |
![]() |
|||||
C00037557
![]() |
N-Methylpyrrolidinylhygrine
/ N-Methylpyrrolidinylhygrine A |
No. 2565 | No. 1 |
![]() |
||||
C00002034
![]() |
Cuscohygrine
/ meso-Cuscohygrine |
C098327
|
No. 2565 | No. 1 |
![]() |
|||
C00002306
![]() |
Tropine
|
CHEMBL113555
CHEMBL1356617 CHEMBL2165231 |
C005864
|
6 / 13 / 13 | No. 2640 | No. 1 |
![]() |
|
C00002046
![]() |
(+)-Hygrine
|
CHEMBL315140
|
C015946
|
No. 3745 | No. 1 |
![]() |
||
C00002299
![]() |
Physoperuvine
|
No. 5790 | No. 1 |
![]() |
||||
C00036318
![]() |
(+)-Physoperuvine
|
No. 7451 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UBT6 | DNA polymerase kappa | Enzyme | C00005160 C00005169 C00005401 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005160 C00005169 C00005401 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005160 C00005169 C00005401 | 1 / 0 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00005160 C00005169 C00005401 | 1 / 1 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005160 C00005169 C00005401 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00005160 C00005169 C00005401 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00005160 C00005169 | 2 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005160 C00005169 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00005160 C00005169 | 0 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00005160 C00005169 | 1 / 1 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00005160 C00005169 | 0 / 0 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00005160 C00005169 | 1 / 4 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005160 C00005169 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005160 C00005169 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005160 C00005169 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00005160 C00005169 | 2 / 3 |
P39748 | Flap endonuclease 1 | Enzyme | C00005160 C00005169 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00005160 C00005169 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00005160 C00005169 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005160 C00005169 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005160 C00005169 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00005160 C00005169 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002306 C00005401 | 0 / 1 |
P14679 | Tyrosinase | Oxidoreductase | C00005401 | 4 / 2 |
P06276 | Cholinesterase | Hydrolase | C00005401 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00005401 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002306 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00005401 | 3 / 3 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00005401 | 2 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00005401 | 1 / 1 |
P22303 | Acetylcholinesterase | Hydrolase | C00005401 | 1 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002306 | 1 / 1 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00005401 | 0 / 0 |
P27487 | Dipeptidyl peptidase 4 | S9B | C00005401 | 0 / 1 |
P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00005401 | 0 / 0 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00005401 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00005401 | 4 / 3 |
P48147 | Prolyl endopeptidase | S9A | C00005401 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002306 | 0 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005401 | 0 / 0 |
P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00005401 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00005401 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00002306 | 11 / 10 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00005401 | 0 / 3 |
P33527 | Multidrug resistance-associated protein 1 | drugs | C00005401 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002306 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#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 |
Q14191
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#615363 | Estrogen resistance; estrr |
P03372
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#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
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
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)
|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00032 | Thyroid cancer |
P27487
(marker)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(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)
|