Organism name | Penstemon grandiflorus |
---|---|
Genus | Penstemon |
Family | Plantaginaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Penstemon grandiflorus |
---|---|
Linked NCBI taxonomy ID | 379497 |
Linked level | species |
Family in NCBI taxonomy | Plantaginaceae |
---|---|
ID | 156152 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
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
![]() |
Cornin
/ Verbenalin |
CHEMBL1080178
CHEMBL1375107 |
C000511
|
5 / 9 / 10 | No. 56 | No. 36 |
![]() |
|
C00010576
![]() |
Hastatoside
|
No. 56 | No. 36 |
![]() |
||||
C00010658
![]() |
Penstemoside
/ Pedicularioside |
CHEMBL463960
|
C079206
|
No. 56 | No. 36 |
![]() |
||
C00040760
![]() |
10-Hydroxycornin
/ (-)-10-Hydroxycornin |
No. 56 | No. 36 |
![]() |
||||
C00040852
![]() |
8-Epihastatoside
|
No. 56 | No. 36 |
![]() |
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 |
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 | 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)
|