Artemisia keiskeana
Species
KNApSAcK Entry
| Organism name | Artemisia keiskeana |
|---|---|
| Genus | Artemisia |
| Family | Asteraceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Artemisia keiskeana |
|---|---|
| Linked NCBI taxonomy ID | 637481 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Asteraceae |
|---|---|
| ID | 4210 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | asterids |
|---|---|
| ID | 71274 |
Metabolite list (7)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00045668
|
Artekeiskeanol D
|
CHEMBL465505
CHEMBL465492 |
No. 335 |
|
||||
|
C00045667
|
Artekeiskeanol C
|
CHEMBL465505
CHEMBL465492 |
No. 335 |
|
||||
|
C00045666
|
Artekeiskeanol B
|
CHEMBL465504
CHEMBL454286 |
No. 335 |
|
||||
|
C00045665
|
Artekeiskeanol A
|
CHEMBL465504
CHEMBL454286 |
No. 335 |
|
||||
|
C00030527
|
Isofraxidin
|
CHEMBL451518
|
C008182
|
No. 364 | No. 25 |
|
||
|
C00019875
|
Fraxidin
|
CHEMBL2334351
|
6 / 2 / 4 | No. 364 | No. 25 |
|
||
|
C00002463
|
Daphnoretin
|
CHEMBL508494
|
C035316
|
14 / 11 / 10 | No. 1906 | No. 25 |
|
Human Protein / Gene in interactions
20 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P06746 | DNA polymerase beta | Enzyme | C00002463 | 0 / 0 |
| P43166 | Carbonic anhydrase 7 | Lyase | C00019875 | 0 / 0 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002463 | 0 / 0 |
| Q8N1Q1 | Carbonic anhydrase 13 | Lyase | C00019875 | 0 / 0 |
| P00918 | Carbonic anhydrase 2 | Lyase | C00019875 | 1 / 2 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002463 | 1 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002463 | 0 / 0 |
| O43570 | Carbonic anhydrase 12 | Lyase | C00019875 | 1 / 2 |
| O75496 | Geminin | Unclassified protein | C00002463 | 0 / 0 |
| P00915 | Carbonic anhydrase 1 | Lyase | C00019875 | 0 / 0 |
| Q16790 | Carbonic anhydrase 9 | Lyase | C00019875 | 0 / 1 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002463 | 3 / 3 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002463 | 2 / 2 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002463 | 0 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00002463 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002463 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00002463 | 4 / 3 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00002463 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002463 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002463 | 1 / 1 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (13)
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #143860 | Hyperchlorhidrosis, isolated |
O43570
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG DISEASE (14)
| KEGG | name | UniProt |
|---|---|---|
| H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
| H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| 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)
|
| 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)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|