PCIDB

Musa x paradisiaca

Species

KNApSAcK Entry

Organism name Musa x paradisiaca
Genus Musa
Family Musaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Musa x paradisiaca
Linked NCBI taxonomy ID 89151
Linked level species

Family

Family in NCBI taxonomy Musaceae
ID 4637

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

Metabolite list (6)

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 External link 512 Malvidin 3-rutinoside
No. 1 No. 15
C00002376 External link 512 Cyanidin 3-rutinoside
CHEMBL505251
C020386
3 / 0 / 1 No. 1 No. 15
C00006639 External link 512 Pelargonidin 3-rutinoside
No. 1 No. 15
C00006703 External link 512 Vincanin B
/ Delphinidin 3-(6-rhamnosylgalactoside)
No. 1 No. 15
C00006686 External link 512 Peonidin 3-rutinoside
No. 1 No. 15
C00001915 External link 512 Salsolinol
/ (-)-Salsolinol
CHEMBL416732
CHEMBL1193327
CHEMBL1195032
14 / 11 / 9 No. 2962 No. 4

Human Protein / Gene in interactions

17 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

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 DISEASE (10)

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)