| Organism name | Eucalyptus tereticornis |
|---|---|
| Genus | Eucalyptus |
| Family | Myrtaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Eucalyptus tereticornis |
|---|---|
| Linked NCBI taxonomy ID | 183855 |
| Linked level | species |
| Family in NCBI taxonomy | Myrtaceae |
|---|---|
| ID | 3931 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00036480
|
Colosic acid
/ 2alpha-Hydroxyursolic acid |
CHEMBL391533
CHEMBL237535 CHEMBL391534 CHEMBL574993 |
C113861
|
17 / 7 / 6 | No. 13 | No. 51 |
|
|
|
C00037978
|
Ursolic acid lactone
|
CHEMBL1590724
|
2 / 4 / 4 | No. 23 | No. 51 |
|
||
|
C00029633
|
Ursolic acid
/ Acetylursolic acid |
CHEMBL55086
CHEMBL410525 |
4 / 2 / 2 | No. 177 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P06746 | DNA polymerase beta | Enzyme | C00029633 C00036480 | 0 / 0 |
| P18433 | Receptor-type tyrosine-protein phosphatase alpha | Receptor tyrosine-protein phosphatase | C00036480 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00036480 | 1 / 1 |
| P11217 | Glycogen phosphorylase, muscle form | Enzyme | C00036480 | 1 / 1 |
| P10586 | Receptor-type tyrosine-protein phosphatase F | Receptor tyrosine-protein phosphatase | C00036480 | 0 / 0 |
| P28845 | Corticosteroid 11-beta-dehydrogenase isozyme 1 | Enzyme | C00036480 | 1 / 1 |
| P42858 | Huntingtin | Unclassified protein | C00036480 | 1 / 1 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00036480 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00036480 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00036480 | 0 / 0 |
| P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00029633 | 2 / 2 |
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00036480 | 0 / 0 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00036480 | 0 / 0 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00037978 | 0 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00029633 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00037978 | 4 / 3 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00036480 | 0 / 0 |
| P17706 | Tyrosine-protein phosphatase non-receptor type 2 | Tyr | C00036480 | 0 / 1 |
| P29350 | Tyrosine-protein phosphatase non-receptor type 6 | Tyr | C00036480 | 0 / 0 |
| P80365 | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Enzyme | C00036480 | 1 / 1 |
| P23469 | Receptor-type tyrosine-protein phosphatase epsilon | Receptor tyrosine-protein phosphatase | C00036480 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00029633 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #218030 | Apparent mineralocorticoid excess; ame |
P80365
|
| #613546 | Aromatase deficiency |
P11511
|
| #139300 | Aromatase excess syndrome; aexs |
P11511
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #604931 | Cortisone reductase deficiency 1; cortrd1 |
P28845
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #232600 | Glycogen storage disease v |
P11217
|
| #143100 | Huntington disease; hd |
P42858
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| KEGG | name | UniProt |
|---|---|---|
| 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)
|
| H00069 | Glycogen storage diseases (GSD) |
P11217
(related)
|
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
| H00794 | Aromatase excess syndrome |
P11511
(related)
|
| H00408 | Type I diabetes mellitus |
P17706
(related)
|
| H01111 | Cortisone reductase deficiency (CRD) |
P28845
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00259 | Apparent mineralocorticoid excess syndrome |
P80365
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|