Species

KNApSAcK Entry

Organism name Juniperus spp.
Genus Juniperus
Family Cupressaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Juniperus
Linked NCBI taxonomy ID 13100
Linked level genus

Family

Family in NCBI taxonomy Cupressaceae
ID 3367

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Metabolite list (27)

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
C00005408 External link 512 Quercetin 3-galactosyl-(1->6)-glucoside
CHEMBL1097317
No. 1 No. 15
C00005404 External link 512 Quercetin 3-vicianoside
CHEMBL451224
No. 1 No. 15
C00001015 External link 512 Amentoflavone
CHEMBL63354
C011164
50 / 39 / 29 5 / 0 No. 34 No. 18
C00001034 External link 512 Cupressuflavone
CHEMBL1208973
6 / 1 / 1 No. 34 No. 18
C00001049 External link 512 Hinokiflavone
CHEMBL291426
C060299
2 / 1 / 2 No. 34 No. 18
C00006535 External link 512 Isocryptomerin
No. 34 No. 18
C00006490 External link 512 Podocarpusflavone A
CHEMBL220745
C094150
2 / 1 / 2 No. 34 No. 18
C00001094 External link 512 Robustaflavone
CHEMBL63677
2 / 1 / 3 No. 34 No. 18
C00005958 External link 512 Quercetin 3-(6''-galloylglucoside)
CHEMBL499432
No. 98
C00002598 External link 512 Yatein
/ (-)-Yatein
/ (-)-Deoxypodorhizone
/ Dihydroanhydropodorhizol
CHEMBL345590
CHEMBL471067
CHEMBL2021357
C452802
2 / 1 / 1 No. 223 No. 21
C00012510 External link 512 (-)-Cuparene
/ (S)-(-)-Cuparene
/ (S)-1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene
No. 309
C00003110 External link 512 Caryophyllene
/ (E)-Caryophyllene
/ beta-Caryophyllene
/ (-)-(E)-Caryophyllene
/ (E)-beta-Caryophyllene
CHEMBL445740
CHEMBL448700
2 / 3 / 7 No. 478 No. 38
C00010932 External link 512 (S)-(-)-alpha-Terpineol
/ (S)-(-)-p-Menth-1-en-8-ol
CHEMBL447597
CHEMBL449810
3 / 16 / 11 No. 983 No. 35
C00010931 External link 512 (R)-(+)-alpha-Terpineol
/ (R)-(+)-p-Menth-1-en-8-ol
CHEMBL447597
CHEMBL449810
3 / 16 / 11 No. 983 No. 35
C00011011 External link 512 alpha-Thujaplicin
/ 2-Hydroxy-3-isopropyl-2,4,6-cycloheptatrien-1-one
CHEMBL1275969
No. 1304 No. 35
C00000831 External link 512 (+)-trans-Sabinol
C052984
No. 1343 No. 35
C00010873 External link 512 (-)-beta-Phellandrene
CHEMBL444254
No. 1898 No. 35
C00003051 External link 512 alpha-Phellandrene
CHEMBL455041
C005403
No. 1898 No. 35
C00003052 External link 512 (+)-beta-Phellandrene
CHEMBL444254
No. 1898 No. 35
C00003061 External link 512 gamma-Terpinene
/ 1-Methyl-4-(1-methylethyl)-1,4-cyclohexadiene
CHEMBL449693
C018669
No. 2468 No. 35
C00003060 External link 512 alpha-Terpinene
No. 2468 No. 35
C00011044 External link 512 (+)-Carene
CHEMBL506854
No. 2690 No. 35
C00011962 External link 512 Nootkatin
CHEMBL1700891
6 / 1 / 1 No. 3130
C00000861 External link 512 Terpinolene
CHEMBL454697
C027009
1 / 0 No. 3725
C00010825 External link 512 Isocineple
/ 1,4-Cineole
C058951
No. 4112 No. 35
C00011009 External link 512 beta-Dolabrin
C410956
No. 4728
C00010311 External link 512 (S)-Citronellic acid
/ (S)-3,7-Dimethyl-6-octenoic acid
No. 8694

Human Protein / Gene in interactions

58 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P56817 Beta-secretase 1 A1A C00001015 C00001034 C00001049 C00001094 C00006490 0 / 0
P43235 Cathepsin K C1A C00001015 C00001049 C00006490 1 / 2
Q9UNA4 DNA polymerase iota Enzyme C00001015 C00001034 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001015 C00011962 0 / 0
P02545 Prelamin-A/C Unclassified protein C00010931 C00010932 11 / 10
Q9UBT6 DNA polymerase kappa Enzyme C00001015 C00001034 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00010931 C00010932 5 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00001015 C00011962 0 / 0
O00255 Menin Unclassified protein C00001015 C00003110 2 / 5
P08253 72 kDa type IV collagenase M10A C00001015 C00001094 1 / 3
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00010931 C00010932 3 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001015 C00003110 1 / 2
Q9Y253 DNA polymerase eta Enzyme C00001015 C00001034 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001015 C00011962 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001015 C00001034 0 / 0
O75496 Geminin Unclassified protein C00001034 C00011962 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002598 0 / 1
P35462 D(3) dopamine receptor Dopamine receptor C00001015 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00001015 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00001015 2 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00001015 7 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00001015 0 / 0
P15692 Vascular endothelial growth factor A Secreted protein C00001015 1 / 2
P47712 Cytosolic phospholipase A2 Enzyme C00001015 0 / 0
P14555 Phospholipase A2, membrane associated Enzyme C00001015 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001015 2 / 2
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001015 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001015 0 / 0
P19174 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 Enzyme C00001015 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001015 2 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001015 0 / 0
P49763 Placenta growth factor Unclassified protein C00001015 0 / 0
O15496 Group 10 secretory phospholipase A2 Enzyme C00001015 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001015 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00011962 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001015 3 / 1
P55072 Transitional endoplasmic reticulum ATPase Unclassified protein C00001015 2 / 1
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00001015 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002598 1 / 0
Q9UN88 Gamma-aminobutyric acid receptor subunit theta GABA-A theta C00001015 0 / 0
P28472 Gamma-aminobutyric acid receptor subunit beta-3 GABA-A beta C00001015 1 / 0
P14867 Gamma-aminobutyric acid receptor subunit alpha-1 GABA-A alpha C00001015 1 / 1
P48169 Gamma-aminobutyric acid receptor subunit alpha-4 GABA-A alpha C00001015 0 / 0
O14764 Gamma-aminobutyric acid receptor subunit delta GABA-A delta C00001015 1 / 1
P31644 Gamma-aminobutyric acid receptor subunit alpha-5 GABA-A alpha C00001015 0 / 0
Q99928 Gamma-aminobutyric acid receptor subunit gamma-3 GABA-A gamma C00001015 0 / 0
P78334 Gamma-aminobutyric acid receptor subunit epsilon GABA-A epsilon C00001015 0 / 0
Q8N1C3 Gamma-aminobutyric acid receptor subunit gamma-1 GABA-A gamma C00001015 0 / 0
P34903 Gamma-aminobutyric acid receptor subunit alpha-3 GABA-A alpha C00001015 0 / 0
O00591 Gamma-aminobutyric acid receptor subunit pi GABA-A pi C00001015 0 / 0
P47870 Gamma-aminobutyric acid receptor subunit beta-2 GABA-A beta C00001015 0 / 0
P18507 Gamma-aminobutyric acid receptor subunit gamma-2 GABA-A gamma C00001015 4 / 2
P18505 Gamma-aminobutyric acid receptor subunit beta-1 GABA-A beta C00001015 0 / 0
Q16445 Gamma-aminobutyric acid receptor subunit alpha-6 GABA-A alpha C00001015 0 / 0
P47869 Gamma-aminobutyric acid receptor subunit alpha-2 GABA-A alpha C00001015 1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001015 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00001015 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00011962 1 / 1

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001015
1638 DCT, TRP-2, TYRP2 dopachrome tautomerase (EC:5.3.3.12) C00001015
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00001015
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) C00001015
7299 TYR, ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3 tyrosinase (EC:1.14.18.1) C00001015
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00000861

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (57)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103780 Alcohol dependence P47869
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613954 Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia; als14 P55072
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#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
Q14191
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#119900 Digital clubbing, isolated congenital P15428
#607208 Dravet syndrome P18507
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#607681 Epilepsy, childhood absence, susceptibility to, 2; eca2 P18507
#612269 Epilepsy, childhood absence, susceptibility to, 5; eca5 P28472
#613060 Epilepsy, idiopathic generalized, susceptibility to, 10; eig10 O14764
#611136 Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 P14867
#600274 Frontotemporal dementia; ftd P10636
#604233 Generalized epilepsy with febrile seizures plus, type 1; gefsp1 P18507
#611277 Generalized epilepsy with febrile seizures plus, type 3; gefsp3 P18507
#143500 Gilbert syndrome P22309
P22310
#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
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#167320 Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1; ibmpfd1 P55072
#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
#603933 Microvascular complications of diabetes, susceptibility to, 1; mvcd1 P15692
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#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
#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
#265800 Pycnodysostosis P43235
#275210 Restrictive dermopathy, lethal P02545
#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
#190300 Tremor, hereditary essential, 1; etm1 P35462
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (41)

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)
H00783 Febrile seizures O14764 (related)
P18507 (related)
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)
H00025 Penile cancer P08253 (related)
H00028 Choriocarcinoma P08253 (related)
H00472 Torg-Winchester syndrome P08253 (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)
P55072 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00808 Idiopathic generalized epilepsies (IGEs) P14867 (related)
P18507 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00018 Gastric cancer P15692 (related)
H00021 Renal cell carcinoma P15692 (marker)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00208 Hyperbilirubinemia P22309 (related)
H00273 Pycnodysostosis P43235 (related)
H00425 Lysosomal cysteine protease deficiencies P43235 (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)
H00296 Defects in RecQ helicases Q14191 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)