Species

KNApSAcK Entry

Organism name Lepidozia fauriana
Genus Lepidozia
Family Lepidoziaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lepidozia fauriana
Linked NCBI taxonomy ID 989928
Linked level species

Family

Family in NCBI taxonomy Lepidoziaceae
ID 13806

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Embryophyta
ID 3193

Metabolite list (21)

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
C00021720 External link 512 beta-Cedrene
/ (+)-beta-Cedrene
No. 149 No. 38
C00029817 External link 512 beta-Longipinene
/ (-)-beta-Longipinene
No. 149 No. 38
C00003112 External link 512 Cedrol
/ (+)-Cedrol
/ alpha-Cedrol
CHEMBL1592444
CHEMBL1974890
C078669
5 / 14 / 11 No. 161 No. 38
C00036710 External link 512 alpha-Copane
No. 197 No. 38
C00021217 External link 512 Himbaccol
/ Viridiflorol
CHEMBL2171207
1 / 2 / 3 No. 197 No. 38
C00021213 External link 512 Globulol
/ (-)-Globulol
CHEMBL2171207
1 / 2 / 3 No. 197 No. 38
C00016959 External link 512 Maaliol
/ (+)-Maaliol
/ Maali alcohol
No. 197 No. 38
C00035520 External link 512 alpha-Amorphene
No. 283 No. 39
C00003203 External link 512 alpha-Ylangene
No. 333 No. 38
C00003194 External link 512 Thujopsene
No. 365 No. 38
C00021886 External link 512 beta-Pompene
/ Gymnomitrene
/ beta-Barbatene
/ beta-Gymnomitrene
No. 365 No. 38
C00003110 External link 512 Caryophyllene
/ (E)-Caryophyllene
/ beta-Caryophyllene
/ (-)-(E)-Caryophyllene
/ (E)-beta-Caryophyllene
CHEMBL445740
CHEMBL448700
2 / 3 / 7 No. 478 No. 38
C00037332 External link 512 Isoledene
/ (-)-Isoledene
No. 595 No. 38
C00021230 External link 512 Aromadendrene
/ (+)-Aromadendrene
/ (+)-Aromadendr-7(15)-ene
CHEMBL509805
CHEMBL596664
No. 640
C00021229 External link 512 Alloaromadendrene
/ allo-Aromadendrene
CHEMBL509805
CHEMBL596664
No. 640
C00036272 External link 512 (-)-Bicyclogermacrene
/ ent-Bicyclogermacrene
CHEMBL509566
No. 699 No. 38
C00037346 External link 512 Isosativene
No. 974
C00007453 External link 512 Cyclohexane
/ beta-Elemene
CHEMBL448502
CHEMBL479707
No. 1400
C00012518 External link 512 delta-Cuprenene
/ (-)-delta-Cuprenene
/ [R-(R*,S*)]-3-Methylene-6-(1,2,2-trimethylcyclopentyl)cyclohexene
No. 2555
C00012011 External link 512 delta-Elemene
No. 4001
C00036302 External link 512 (+)-Dihydrochiloscypholone
No. 5193

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00021213 C00021217 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00003112 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003112 0 / 0
P02545 Prelamin-A/C Unclassified protein C00003112 11 / 10
P10828 Thyroid hormone receptor beta NR1A2 C00003112 3 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00003112 0 / 0
O00255 Menin Unclassified protein C00003110 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003110 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#114550 Hepatocellular carcinoma P08581
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#275210 Restrictive dermopathy, lethal P02545
#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

KEGG DISEASE (21)

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)
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)
H00018 Gastric cancer P08581 (related)
H00021 Renal cell carcinoma P08581 (related)
H00046 Cholangiocarcinoma P08581 (related)
H00249 Thyroid hormone resistance syndrome P10828 (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)