Species

KNApSAcK Entry

Organism name Papaver fugax Poir.
Genus Papaver
Family Papaveraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Papaver
Linked NCBI taxonomy ID 3468
Linked level genus

Family

Family in NCBI taxonomy Papaveraceae
ID 3465

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (2)

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
C00001810 External link 512 Armepavine
/ (-)-Armepavine
/ (R)-(-)-Armepavine
CHEMBL451722
CHEMBL1186477
CHEMBL1186510
7 / 5 / 3 No. 345 No. 4
C00026134 External link 512 Mecambridine
/ (-)-Oreophiline
/ (-)-Mecambridine
C051429
No. 3042

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00001810 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001810 2 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001810 3 / 3
P16050 Arachidonate 15-lipoxygenase Enzyme C00001810 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001810 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001810 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001810 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#114500 Colorectal cancer; crc P84022
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (3)

KEGG name UniProt
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)