PCIDB

Erysimum cheiranthoides

Species

KNApSAcK Entry

Organism name Erysimum cheiranthoides
Genus Erysimum
Family Cruciferae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Erysimum cheiranthoides
Linked NCBI taxonomy ID 330168
Linked level species

Family

Family in NCBI taxonomy Brassicaceae
ID 3700

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

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
C00001473 External link 512 Glucoiberverin
/ 3-(Methylthio)propyl glucosinolate
No. 46 No. 76
C00007344 External link 512 Glucoerucin
/ 4-Methylthiobutyl glucosinolate
C119493
No. 46 No. 76
C00003625 External link 512 Helveticoside
CHEMBL1551151
C007914
11 / 18 / 15 No. 109 No. 56
C00032810 External link 512 Cheiranthoside IX
CHEMBL1169677
No. 272 No. 56
C00032811 External link 512 Cheiranthoside X
No. 272 No. 56

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003625 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00003625 4 / 1
Q99700 Ataxin-2 Unclassified protein C00003625 1 / 1
P02545 Prelamin-A/C Unclassified protein C00003625 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003625 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00003625 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00003625 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00003625 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003625 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003625 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003625 0 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

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
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (15)

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)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)