Organism name | Satureja acinos |
---|---|
Genus | Satureja |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Satureja |
---|---|
Linked NCBI taxonomy ID | 49986 |
Linked level | genus |
Family in NCBI taxonomy | Lamiaceae |
---|---|
ID | 4136 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
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 |
---|---|---|---|---|---|---|---|---|
C00029633
![]() |
Ursolic acid
/ Acetylursolic acid |
CHEMBL55086
CHEMBL410525 |
4 / 2 / 2 | No. 177 |
![]() |
|||
C00019308
![]() |
Doursterol
/ Daucosterin / 3-O-beta-D-Glucopyranosyl sitosterol / beta-Sitosterol 3-O-beta-D-glucopyranoside |
CHEMBL197711
CHEMBL506678 CHEMBL2304043 |
C011015
|
5 / 4 / 2 | 0 / 3 | No. 520 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P06746 | DNA polymerase beta | Enzyme | C00019308 C00029633 | 0 / 0 |
P00734 | Prothrombin | S1A | C00019308 | 4 / 2 |
P08047 | Transcription factor Sp1 | Unclassified protein | C00019308 | 0 / 0 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00019308 | 0 / 0 |
P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00019308 | 0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00029633 | 2 / 2 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00029633 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00029633 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#601367 | Stroke, ischemic |
P00734
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|