Species

KNApSAcK Entry

Organism name Pieris formosa
Genus Pieris
Family Ericaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pieris formosa
Linked NCBI taxonomy ID 49158
Linked level species

Family

Family in NCBI taxonomy Ericaceae
ID 4345

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (6)

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
C00040879 External link 512 Asebotoxin IV
No. 320 No. 45
C00041086 External link 512 Pierisformosin B
CHEMBL169864
No. 320 No. 45
C00041087 External link 512 Pierisformosin C
/ (-)-Pierisformosin C
No. 320 No. 45
C00050196 External link 512 Pierisformosin D
/ (+)-Pierisformosin D
No. 320 No. 45
C00050006 External link 512 Asebotoxin V
CHEMBL1610188
4 / 15 / 11 No. 320 No. 45
C00050195 External link 512 Pierisformoside A
/ (-)-Pierisformoside A
No. 4673

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00050006 4 / 1
P02545 Prelamin-A/C Unclassified protein C00050006 11 / 10
O75496 Geminin Unclassified protein C00050006 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00050006 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

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
#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
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637

KEGG DISEASE (11)

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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)