Species

KNApSAcK Entry

Organism name Nelumbo nucifera
Genus Nelumbo
Family Nelumbonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Nelumbo nucifera
Linked NCBI taxonomy ID 4432
Linked level species

Family

Family in NCBI taxonomy Nelumbonaceae
ID 4429

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

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
C00001807 External link 512 Anonaine
/ (-)-Anonaine
/ (R)-Annonaine
CHEMBL401798
C098138
1 / 0 / 0 No. 20 No. 4
C00028473 External link 512 Liensinine
C080095
No. 89 No. 4
C00001810 External link 512 Armepavine
/ (-)-Armepavine
/ (R)-(-)-Armepavine
CHEMBL451722
CHEMBL1186477
CHEMBL1186510
7 / 5 / 3 No. 345 No. 4
C00001905 External link 512 Milthanthine
/ Pronuciferine
/ (+)-Pronuciferine
/ N-Methylstepharine
/ N,O-Dimethylcrotonosine
CHEMBL237766
No. 688

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001807 0 / 0
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)