Species

KNApSAcK Entry

Organism name Artemisia campestris
Genus Artemisia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Artemisia campestris
Linked NCBI taxonomy ID 72337
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 (11)

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
C00004567 External link 512 Rhamnocitrin
/ 7-Methylkaempferol
/ 3,4',5-Trihydroxy-7-methoxyflavone
/ 3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
CHEMBL442289
No. 3 No. 15
C00004642 External link 512 Rhamnazin
/ 7,3'-Di-O-methylquercetin
/ 3,4',5-Trihydroxy-3',7-dimethoxyflavone
/ 3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
CHEMBL457148
No. 3 No. 15
C00003849 External link 512 Isocutellarein 7-methyl ether
/ 5,8,4'-Trihydroxy-7-methoxyflavone
No. 3 No. 15
C00000969 External link 512 Homoeriodictyol
CHEMBL398282
CHEMBL490170
4 / 4 / 4 No. 25 No. 14
C00000999 External link 512 Sakuranetin
/ Naringenin 7-O-methyl ether
/ 5,4'-Dihydroxy-7-methoxyflavanone
CHEMBL74852
CHEMBL448297
C099724
19 / 20 / 20 No. 25 No. 14
C00008392 External link 512 5,8,4'-Trihydroxyflavanone
No. 25 No. 14
C00008391 External link 512 5,6-Dihydroxy-4'-methoxyflavanone
No. 25 No. 14
C00000973 External link 512 Isosakuranetin
/ 5,7-Dihydroxy-4'-methoxyflavanone
CHEMBL470266
3 / 4 / 4 No. 25 No. 14
C00004573 External link 512 3,7,4'-Tri-O-methylkaempferol
/ Kaempferol 3,7,4'-trimethyl ether
/ 5-Hydroxy-3,7,4'-trimethoxyflavone
/ 5-Hydroxy-3,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL77686
No. 35 No. 15
C00008577 External link 512 Padmatin
No. 42 No. 14
C00001279 External link 512 Dehydrofalcarinone
No. 1184

Human Protein / Gene in interactions

23 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000969 C00000973 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000969 C00000973 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000969 C00000973 4 / 4
O75496 Geminin Unclassified protein C00000999 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000999 0 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00000999 1 / 4
Q99700 Ataxin-2 Unclassified protein C00000999 1 / 1
P11473 Vitamin D3 receptor NR1I1 C00000999 2 / 3
Q9Y3R4 Sialidase-2 Enzyme C00000999 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000999 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000999 2 / 0
P04062 Glucosylceramidase Enzyme C00000999 6 / 4
Q9Y253 DNA polymerase eta Enzyme C00000999 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00000999 0 / 0
P06746 DNA polymerase beta Enzyme C00000969 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00000999 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000999 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000999 4 / 3
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000999 1 / 1
P59538 Taste receptor type 2 member 31 Taste receptor (taste family GPCR) C00000999 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00000999 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000999 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000999 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#208900 Ataxia-telangiectasia; at Q13315
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#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
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (24)

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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)