Species

KNApSAcK Entry

Organism name Selinum vaginatum
Genus Selinum
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Selinum vaginatum
Linked NCBI taxonomy ID 239673
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 (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
C00008235 External link 512 Selinone
No. 28 No. 14
C00033081 External link 512 Selinidin
/ Selenedin
/ Jatamansin
/ Secryptotaenin A
CHEMBL457257
CHEMBL1321343
9 / 6 / 7 No. 858 No. 25
C00002450 External link 512 Angelicin
CHEMBL53569
C011659
2 / 0 / 0 0 / 3 No. 1282 No. 25
C00021410 External link 512 Vaginatin
/ Crispanone
No. 1621

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00033081 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00033081 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00033081 0 / 0
P56817 Beta-secretase 1 A1A C00002450 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00033081 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00033081 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00033081 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00002450 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00033081 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00033081 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00033081 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#119900 Digital clubbing, isolated congenital P15428
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (7)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00002450
D056486 Drug-Induced Liver Injury C00002450
D010787 Photosensitivity Disorders C00002450