Organism name | Musa x paradisiaca |
---|---|
Genus | Musa |
Family | Musaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Musa x paradisiaca |
---|---|
Linked NCBI taxonomy ID | 89151 |
Linked level | species |
Family in NCBI taxonomy | Musaceae |
---|---|
ID | 4637 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Liliopsida |
---|---|
ID | 4447 |
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 |
---|---|---|---|---|---|---|---|---|
C00006740 |
Malvidin 3-rutinoside
|
No. 1 | No. 15 | |||||
C00002376 |
Cyanidin 3-rutinoside
|
CHEMBL505251
|
C020386
|
3 / 0 / 1 | No. 1 | No. 15 | ||
C00006639 |
Pelargonidin 3-rutinoside
|
No. 1 | No. 15 | |||||
C00006703 |
Vincanin B
/ Delphinidin 3-(6-rhamnosylgalactoside) |
No. 1 | No. 15 | |||||
C00006686 |
Peonidin 3-rutinoside
|
No. 1 | No. 15 | |||||
C00001915 |
Salsolinol
/ (-)-Salsolinol |
CHEMBL416732
CHEMBL1193327 CHEMBL1195032 |
14 / 11 / 9 | No. 2962 | No. 4 |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001915 | 1 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00001915 | 1 / 1 |
Q07812 | Apoptosis regulator BAX | Unclassified protein | C00002376 | 0 / 1 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001915 | 3 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001915 | 0 / 1 |
P14416 | D(2) dopamine receptor | Dopamine receptor | C00001915 | 2 / 0 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00001915 | 0 / 0 |
P21917 | D(4) dopamine receptor | Dopamine receptor | C00001915 | 0 / 0 |
Q16611 | Bcl-2 homologous antagonist/killer | Unclassified protein | C00002376 | 0 / 0 |
O43521 | Bcl-2-like protein 11 | Unclassified protein | C00002376 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001915 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001915 | 3 / 3 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001915 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001915 | 0 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001915 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001915 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001915 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#103780 | Alcohol dependence |
P14416
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#159900 | Myoclonic dystonia |
P14416
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00020 | Colorectal cancer |
Q07812
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|