| Organism name | Psilopeganum sinense |
|---|---|
| Genus | Psilopeganum |
| Family | Rutaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Psilopeganum sinense |
|---|---|
| Linked NCBI taxonomy ID | 405848 |
| Linked level | species |
| Family in NCBI taxonomy | Rutaceae |
|---|---|
| ID | 23513 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00002456
|
Chalepensin
|
CHEMBL1333931
|
C020740
|
7 / 8 / 6 | No. 3930 | No. 25 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00002456 | 6 / 4 |
| P42858 | Huntingtin | Unclassified protein | C00002456 | 1 / 1 |
| O75496 | Geminin | Unclassified protein | C00002456 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002456 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00002456 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00002456 | 0 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002456 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #143100 | Huntington disease; hd |
P42858
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| KEGG | name | UniProt |
|---|---|---|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|