Species

KNApSAcK Entry

Organism name Sphenosciadium capitellatum
Genus Sphenosciadium
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Sphenosciadium capitellatum
Linked NCBI taxonomy ID 63043
Linked level species

Family

Family in NCBI taxonomy Apiaceae
ID 4037

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
C00002486 External link 512 Nodakenin
CHEMBL459825
C471579
11 / 8 / 6 No. 399 No. 25

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase C00002486 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002486 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002486 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002486 2 / 2
O75496 Geminin Unclassified protein C00002486 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002486 0 / 0
P06280 Alpha-galactosidase A Enzyme C00002486 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002486 2 / 2
P22303 Acetylcholinesterase Hydrolase C00002486 1 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002486 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002486 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#119900 Digital clubbing, isolated congenital P15428
#301500 Fabry disease P06280
#232300 Glycogen storage disease ii P10253
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#112100 Yt blood group antigen P22303

KEGG DISEASE (6)

KEGG name UniProt
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)