PCIDB

Lycopersicon pimpinellifolium Jusl.Mill.

Species

KNApSAcK Entry

Organism name Lycopersicon pimpinellifolium Jusl.Mill.
Genus Lycopersicon
Family Solanaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lycopersicon
Linked NCBI taxonomy ID 49274
Linked level subgenus

Family

Family in NCBI taxonomy Solanaceae
ID 4070

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

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
C00002267 External link 512 Tomatidine
CHEMBL365417
CHEMBL1476096
CHEMBL1622974
CHEMBL1976775
CHEMBL1998601
CHEMBL2165711
C003677
10 / 15 / 14 No. 171 No. 11
C00029023 External link 512 Soladulcidine
CHEMBL365417
CHEMBL1476096
CHEMBL1622974
CHEMBL1976775
CHEMBL1998601
CHEMBL2165711
10 / 15 / 14 No. 171 No. 11

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q15125 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase Enzyme C00002267 C00029023 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002267 C00029023 1 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002267 C00029023 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002267 C00029023 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002267 C00029023 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002267 C00029023 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00002267 C00029023 1 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002267 C00029023 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002267 C00029023 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002267 C00029023 0 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#302960 Chondrodysplasia punctata 2, x-linked dominant; cdpx2 Q15125
#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

KEGG DISEASE (14)

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)
H01194 X-linked chondrodysplasia punctata Q15125 (related)