Species

KNApSAcK Entry

Organism name Achillea nobilis
Genus Achillea
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Achillea nobilis
Linked NCBI taxonomy ID 282753
Linked level species

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
C00014061 External link 512 Isoorientin 2''-O-apiofuranoside
/ 6-(2-O-D-Apio-beta-D-furanosyl-beta-D-glucopyranosyl)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
No. 1 No. 15
C00005498 External link 512 Azaleatin 3-galactoside
No. 2 No. 15
C00004588 External link 512 3,5-Dihydroxy-6,7,8-trimethoxyflavone
/ 3,5-Dihydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one
CHEMBL1416487
8 / 13 / 7 No. 3 No. 15
C00020600 External link 512 Anobin
No. 144 No. 38

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase C00004588 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00004588 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00004588 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00004588 7 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004588 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00004588 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004588 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00004588 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#174800 Mccune-albright syndrome; mas P63092
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

KEGG name UniProt
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)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)