Species

KNApSAcK Entry

Organism name Araucaria angustifolia
Genus Araucaria
Family Araucariaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Araucaria angustifolia
Linked NCBI taxonomy ID 56992
Linked level species

Family

Family in NCBI taxonomy Araucariaceae
ID 25664

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

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
C00002540 External link 512 Irisolidone
/ 4'-O-Methyltectorigenin
/ 5,7-Dihydroxy-6,4'-dimethoxyisoflavone
CHEMBL265945
1 / 0 / 0 No. 3 No. 15
C00006499 External link 512 4',7,7''-Tri-O-methylamentoflavone
/ 7,4',7''-Tri-O-methylamentoflavone
CHEMBL208578
1 / 0 / 0 No. 34 No. 18
C00009405 External link 512 Cabreuvin
/ 7,3',4'-Trimethoxyisoflavone
CHEMBL273891
7 / 10 / 6 No. 35 No. 15
C00000640 External link 512 (+)-Eudesmin
CHEMBL519099
CHEMBL512865
CHEMBL523743
CHEMBL464352
CHEMBL1726879
C105875
2 / 0 / 0 No. 38 No. 21
C00007190 External link 512 (+)-Pinoresinol
CHEMBL267963
CHEMBL487611
CHEMBL460862
C103298
7 / 5 / 6 No. 38 No. 21
C00036233 External link 512 trans-Communic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8 No. 143
C00000604 External link 512 (-)-Secoisolariciresinol
CHEMBL368347
C060283
2 / 1 / 1 1 / 0 No. 282 No. 21
C00007204 External link 512 Isolariciresinol
/ (+)-Isolariciresinol
CHEMBL399512
CHEMBL1760593
C060284
2 / 1 / 1 No. 406
C00037574 External link 512 Octadecyl (E)-p-coumarate
No. 447
C00037573 External link 512 Octadecyl (E)-ferulate
CHEMBL1669148
No. 447
C00037575 External link 512 Octadecyl (Z)-p-coumarate
No. 447
C00002591 External link 512 (-)-Cubebin
/ beta-Cubebin
/ (-)-beta-Cubebin
/ (8R,8'R,9S)-Cubebin
CHEMBL182001
CHEMBL399831
C433065
2 / 1 / 1 0 / 2 No. 629 No. 21
C00000603 External link 512 (-)-Lariciresinol
CHEMBL518421
C060282
2 / 1 / 1 No. 700 No. 21
C00000602 External link 512 (+)-Lariciresinol
CHEMBL518421
2 / 1 / 1 No. 700 No. 21
C00000722 External link 512 cis-Hinokiresinol
CHEMBL198245
CHEMBL199799
CHEMBL371547
CHEMBL451713
C119821
No. 922 No. 24
C00000869 External link 512 Abietal
/ 7,13-Abietadien-18-al
/ Abieta-7,13-diene-18-al
CHEMBL563793
No. 1536 No. 40
C00000871 External link 512 Abietic acid
/ 7,13-Abietadien-18-oic acid
CHEMBL71893
CHEMBL1336124
CHEMBL1357151
CHEMBL1514489
CHEMBL1552001
C023710
18 / 22 / 25 No. 1536 No. 40
C00022482 External link 512 8,14-Labdadien-13beta,19-diol
No. 8408

Human Protein / Gene in interactions

43 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000602 C00000603 C00000604 C00000871 C00002591 C00007204 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000602 C00000603 C00000604 C00002591 C00007204 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000871 C00009405 C00036233 4 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00007190 C00009405 C00036233 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000640 C00036233 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000871 C00036233 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000871 C00007190 0 / 3
O15118 Niemann-Pick C1 protein Unclassified protein C00009405 1 / 1
P11473 Vitamin D3 receptor NR1I1 C00000871 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00000871 0 / 0
P39748 Flap endonuclease 1 Enzyme C00036233 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00000640 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00009405 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00009405 4 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00009405 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00036233 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00036233 1 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000871 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007190 5 / 3
P56817 Beta-secretase 1 A1A C00006499 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000871 3 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000871 0 / 1
P02545 Prelamin-A/C Unclassified protein C00000871 11 / 10
P16050 Arachidonate 15-lipoxygenase Enzyme C00000871 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000871 1 / 1
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00007190 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00036233 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00036233 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00036233 0 / 0
P06746 DNA polymerase beta Enzyme C00036233 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00007190 0 / 0
P05412 Transcription factor AP-1 Transcription Factor C00002540 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00007190 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000871 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000871 0 / 0
Q15118 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial Pdhk C00000871 0 / 0
Q16654 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 4, mitochondrial Pdhk C00000871 0 / 0
Q15119 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 2, mitochondrial Pdhk C00000871 0 / 0
Q15120 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 3, mitochondrial Pdhk C00000871 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00036233 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00007190 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00036233 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00009405 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00000604

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (44)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
%606641 Body mass index; bmi P37231
#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
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#300905 Charcot-marie-tooth disease, x-linked dominant, 6; cmtx6 Q15120
#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
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#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
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (35)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (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)
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)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (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)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00296 Defects in RecQ helicases Q14191 (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)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D004487 Edema C00002591
D010146 Pain C00002591