PCIDB

Heliotropium spp.

Species

KNApSAcK Entry

Organism name Heliotropium spp.
Genus Heliotropium
Family Boraginaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Heliotropium
Linked NCBI taxonomy ID 21621
Linked level genus

Family

Family in NCBI taxonomy Boraginaceae
ID 21571

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (3)

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
C00002089 External link 512 Heliotridine
No. 1675 No. 2
C00002120 External link 512 Supinidine
C011549
No. 1675 No. 2
C00002666 External link 512 Piperonal
CHEMBL271663
C005454
3 / 4 / 4 No. 4093

Human Protein / Gene in interactions

3 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00002666 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002666 3 / 3
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002666 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (4)

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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)