Species

KNApSAcK Entry

Organism name Hernandia ovigera L.
Genus Hernandia
Family Hernandiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Hernandia ovigera
Linked NCBI taxonomy ID 13561
Linked level species

Family

Family in NCBI taxonomy Hernandiaceae
ID 22009

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (5)

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
C00033252 External link 512 N-Methylhernangerine
/ (+)-N-Methylhernangerine
CHEMBL1482066
C073417
7 / 12 / 10 No. 20 No. 4
C00028701 External link 512 N-Methylhernovine
/ (-)-N-Methylhernovine
CHEMBL1183924
No. 20 No. 4
C00027566 External link 512 Nandigerine
/ Hernangerine
/ (+)-Nandigerine
/ (+)-Hernangerine
CHEMBL1190170
No. 20 No. 4
C00027542 External link 512 Hernandonine
No. 74
C00027376 External link 512 Ovigerine
/ Hernovine
/ (+)-Ovigerine
No. 1625

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00033252 0 / 0
P02545 Prelamin-A/C Unclassified protein C00033252 11 / 10
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00033252 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00033252 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00033252 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00033252 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00033252 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (10)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)