Species

KNApSAcK Entry

Organism name Afzelia tortilis
Genus Afzelia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Afzelia
Linked NCBI taxonomy ID 162640
Linked level genus

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (1)

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
C00008823 External link 512 ent-Fisetinidol
CHEMBL1367159
10 / 7 / 7 No. 52 No. 14

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O15296 Arachidonate 15-lipoxygenase B Enzyme C00008823 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00008823 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00008823 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00008823 3 / 3
P16050 Arachidonate 15-lipoxygenase Enzyme C00008823 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00008823 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00008823 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00008823 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00008823 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00008823 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#600274 Frontotemporal dementia; ftd P10636
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)