| Organism name | Hardwickia pinnata |
|---|---|
| Genus | Hardwickia |
| Family | Fabaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Hardwickia |
|---|---|
| Linked NCBI taxonomy ID | 213784 |
| Linked level | genus |
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| 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
|
Kolavic acid
|
No. 221 |
|
|||||
|
C00023495
|
Kolavenol
|
CHEMBL99403
CHEMBL95649 |
No. 221 |
|
||||
|
C00023496
|
Kolavenic acid
|
CHEMBL1517738
|
C072582
|
11 / 7 / 7 | No. 221 |
|
| 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 |
| 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 | 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)
|