Species

KNApSAcK Entry

Organism name Penstemon grandiflorus
Genus Penstemon
Family Plantaginaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Penstemon grandiflorus
Linked NCBI taxonomy ID 379497
Linked level species

Family

Family in NCBI taxonomy Plantaginaceae
ID 156152

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

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
C00003102 External link 512 Cornin
/ Verbenalin
CHEMBL1080178
CHEMBL1375107
C000511
5 / 9 / 10 No. 56 No. 36
C00010576 External link 512 Hastatoside
No. 56 No. 36
C00010658 External link 512 Penstemoside
/ Pedicularioside
CHEMBL463960
C079206
No. 56 No. 36
C00040760 External link 512 10-Hydroxycornin
/ (-)-10-Hydroxycornin
No. 56 No. 36
C00040852 External link 512 8-Epihastatoside
No. 56 No. 36

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003102 2 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00003102 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003102 4 / 3
O00255 Menin Unclassified protein C00003102 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003102 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (10)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)