Organism name | Berberis amurensis |
---|---|
Genus | Berberis |
Family | Berberidaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Berberis amurensis |
---|---|
Linked NCBI taxonomy ID | 258140 |
Linked level | species |
Family in NCBI taxonomy | Berberidaceae |
---|---|
ID | 41773 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | eudicotyledons |
---|---|
ID | 71240 |
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 |
---|---|---|---|---|---|---|---|---|
C00001897
![]() |
Oxyacanthine
|
CHEMBL510022
CHEMBL509999 CHEMBL1983122 |
C092646
|
5 / 4 / 1 | No. 10 | No. 4 |
![]() |
|
C00025342
![]() |
Pseudopalmatine
/ 5,6-Dihydro-8-demethylcoralyne |
CHEMBL376300
|
No. 155 | No. 4 |
![]() |
|||
C00026111
![]() |
Berberrubine
/ 9-Berberoline |
CHEMBL203135
CHEMBL2160119 |
5 / 10 / 6 | No. 155 | No. 4 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00001897 C00026111 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001897 | 1 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001897 | 2 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00001897 | 0 / 0 |
Q09428 | ATP-binding cassette sub-family C member 8 | K | C00026111 | 5 / 3 |
Q14654 | ATP-sensitive inward rectifier potassium channel 11 | K | C00026111 | 3 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00026111 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00026111 | 2 / 1 |
P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00001897 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#606176 | Diabetes mellitus, permanent neonatal; pndm |
Q09428
Q14654 |
#610374 | Diabetes mellitus, transient neonatal, 2 |
Q09428
|
#610582 | Diabetes mellitus, transient neonatal, 3 |
Q14654
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#256450 | Hyperinsulinemic hypoglycemia, familial, 1; hhf1 |
Q09428
|
#601820 | Hyperinsulinemic hypoglycemia, familial, 2; hhf2 |
Q14654
|
#602485 | Hyperinsulinemic hypoglycemia, familial, 3; hhf3 |
Q09428
|
#240800 | Hypoglycemia, leucine-induced; lih |
Q09428
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#277700 | Werner syndrome; wrn |
Q14191
|
KEGG | name | UniProt |
---|---|---|
H00512 | Permanent neonatal diabetes mellitus (PNDM) |
Q09428
(related)
Q14654 (related) |
H00513 | Transient neonatal diabetes mellitus (TNDM) |
Q09428
(related)
Q14654 (related) |
H01267 | Familial hyperinsulinemic hypoglycemia (HHF) |
Q09428
(related)
Q14654 (related) |
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00409 | Type II diabetes mellitus |
Q14654
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|