Species

KNApSAcK Entry

Organism name Acacia willardiana
Genus Acacia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Acacia willardiana
Linked NCBI taxonomy ID 247879
Linked level species

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
C00001399 External link 512 Willardiine
CHEMBL122005
CHEMBL366489
CHEMBL1356611
C002872
14 / 6 / 7 No. 5581

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001399 1 / 0
P48058 Glutamate receptor 4 NS C00001399 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00001399 3 / 2
P42261 Glutamate receptor 1 NS C00001399 0 / 0
Q16478 Glutamate receptor ionotropic, kainate 5 NS C00001399 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001399 0 / 1
P54132 Bloom syndrome protein Enzyme C00001399 1 / 2
P11021 78 kDa glucose-regulated protein Unclassified protein C00001399 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001399 0 / 0
Q04609 Glutamate carboxypeptidase 2 M28B C00001399 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001399 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001399 0 / 1
P42262 Glutamate receptor 2 NS C00001399 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001399 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#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

KEGG DISEASE (7)

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)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)