PCIDB

Artemisia finita

Species

KNApSAcK Entry

Organism name Artemisia finita
Genus Artemisia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Artemisia
Linked NCBI taxonomy ID 4219
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 (1)

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
C00003365 External link 512 beta-Santonin
/ [3R-(3alpha,3abeta,5aalpha,9balpha)]-3a,5,5a,9b-Tetrahydro-3,5a,9-trimethylnaphtho[1,2-b]furan-2,8(3H,4H)-dione
CHEMBL226231
CHEMBL259254
CHEMBL1357930
CHEMBL1570028
CHEMBL1600999
CHEMBL1717567
CHEMBL2103785
14 / 11 / 8 No. 2117 No. 38

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003365 1 / 0
Q99700 Ataxin-2 Unclassified protein C00003365 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00003365 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003365 0 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00003365 0 / 0
O75496 Geminin Unclassified protein C00003365 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003365 7 / 3
P04150 Glucocorticoid receptor NR3C1 C00003365 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003365 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003365 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003365 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00003365 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003365 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003365 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (8)

KEGG name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)