Species

KNApSAcK Entry

Organism name Physalis peruviana
Genus Physalis
Family Solanaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Physalis peruviana
Linked NCBI taxonomy ID 126903
Linked level species

Family

Family in NCBI taxonomy Solanaceae
ID 4070

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (18)

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 External link 512 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 External link 512 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 External link 512 Kaempferol 3-robinobioside
CHEMBL431610
CHEMBL79790
CHEMBL255020
CHEMBL501550
CHEMBL498879
CHEMBL1419228
CHEMBL1875691
22 / 10 / 12 No. 1 No. 15
C00005239 External link 512 Kaempferol 3-rutinoside-7-glucoside
No. 5 No. 15
C00005460 External link 512 Quercetin 3-robinobioside-7-glucoside
No. 5 No. 15
C00005225 External link 512 Kaempferol 3-robinobioside-7-glucoside
No. 5 No. 15
C00039032 External link 512 Dihydrowithanolide E
/ 2,3-Dihydrowithanolide E
No. 176 No. 58
C00040752 External link 512 (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 External link 512 Withaphysanolide
No. 729
C00025557 External link 512 Tigloidin
/ Tigloyl pseudotropine
/ 3beta-Tigloyloxytropane
CHEMBL2107120
CHEMBL2107196
No. 1464 No. 1
C00002304 External link 512 Tigloidine
CHEMBL2107120
CHEMBL2107196
No. 1464 No. 1
C00037123 External link 512 Ethyl 3-hydroxyoctanoate 3-O-beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranoside
No. 2396
C00037557 External link 512 N-Methylpyrrolidinylhygrine
/ N-Methylpyrrolidinylhygrine A
No. 2565 No. 1
C00002034 External link 512 Cuscohygrine
/ meso-Cuscohygrine
C098327
No. 2565 No. 1
C00002306 External link 512 Tropine
CHEMBL113555
CHEMBL1356617
CHEMBL2165231
C005864
6 / 13 / 13 No. 2640 No. 1
C00002046 External link 512 (+)-Hygrine
CHEMBL315140
C015946
No. 3745 No. 1
C00002299 External link 512 Physoperuvine
No. 5790 No. 1
C00036318 External link 512 (+)-Physoperuvine
No. 7451

Human Protein / Gene in interactions

46 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (38)

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 DISEASE (38)

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)