Brassica napus L.ssp.rapifera
Species
KNApSAcK Entry
| Organism name | Brassica napus L.ssp.rapifera |
|---|---|
| Genus | Brassica |
| Family | Cruciferae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Brassica |
|---|---|
| Linked NCBI taxonomy ID | 3705 |
| Linked level | genus |
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 (7)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00026587
|
Brassicanate A
|
No. 2665 |
|
|||||
|
C00026586
|
Isalexin
|
No. 2737 |
|
|||||
|
C00026995
|
Spirobrassinin
/ S-(-)-Spirobrassinin |
No. 3637 |
|
|||||
|
C00027106
|
Brassinin
|
CHEMBL373777
CHEMBL1673034 CHEMBL1673036 CHEMBL1673037 |
C089020
|
5 / 7 / 10 | No. 3839 |
|
||
|
C00027108
|
Brassilexin
|
C430121
|
No. 5488 |
|
||||
|
C00027107
|
Brassicanal A
|
No. 5537 |
|
|||||
|
C00026588
|
Rutalexin
|
No. 8364 |
|
Human Protein / Gene in interactions
5 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P14902 | Indoleamine 2,3-dioxygenase 1 | Enzyme | C00027106 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00027106 | 4 / 3 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00027106 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00027106 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00027106 | 1 / 2 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (7)
| OMIM | preferred title | UniProt |
|---|---|---|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #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)
|