Species

KNApSAcK Entry

Organism name Hardwickia pinnata
Genus Hardwickia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Hardwickia
Linked NCBI taxonomy ID 213784
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
C00023484 External link 512 Kolavic acid
No. 221
C00023495 External link 512 Kolavenol
CHEMBL99403
CHEMBL95649
No. 221
C00023496 External link 512 Kolavenic acid
CHEMBL1517738
C072582
11 / 7 / 7 No. 221

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P17861 X-box-binding protein 1 Unclassified protein C00023496 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00023496 0 / 0
P39748 Flap endonuclease 1 Enzyme C00023496 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00023496 2 / 0
O75496 Geminin Unclassified protein C00023496 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00023496 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00023496 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00023496 2 / 2
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00023496 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00023496 0 / 3
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00023496 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
Q14191
#119900 Digital clubbing, isolated congenital P15428
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#612371 Major affective disorder 7; mafd7 P17861
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (7)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)