Species

KNApSAcK Entry

Organism name Pterodon obliquum
Genus Pterodon
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pterodon
Linked NCBI taxonomy ID 104317
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 (3)

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
C00036202 External link 512 Ptaeroxylin
CHEMBL1527943
7 / 6 / 6 No. 719
C00002442 External link 512 Ptaeroglycol
No. 1000 No. 15
C00002441 External link 512 Perforamone D
/ Ptaerochromenol
CHEMBL2204370
No. 1000 No. 15

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00036202 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00036202 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00036202 2 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00036202 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00036202 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00036202 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00036202 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#119900 Digital clubbing, isolated congenital P15428
#600274 Frontotemporal dementia; ftd P10636
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (6)

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)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)