Species

KNApSAcK Entry

Organism name Tragopogon spp.
Genus Tragopogon
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Tragopogon
Linked NCBI taxonomy ID 13730
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (4)

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
C00006231 External link 512 Lucenin 2
/ Luteolin 6,8-C-diglucoside
No. 1 No. 15
C00006176 External link 512 Vicenin 1
No. 1 No. 15
C00006229 External link 512 Vicenin 2
/ Apigenin 6,8-di-C-glucoside
CHEMBL1442950
6 / 14 / 8 No. 1 No. 15
C00001102 External link 512 Leucanthoside
/ Swertiajaponin
/ 6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone
No. 22 No. 15

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00006229 6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase C00006229 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00006229 7 / 3
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00006229 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00006229 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00006229 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#232300 Glycogen storage disease ii P10253
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#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

KEGG DISEASE (8)

KEGG name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)