Species

KNApSAcK Entry

Organism name Eucalyptus tereticornis
Genus Eucalyptus
Family Myrtaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Eucalyptus tereticornis
Linked NCBI taxonomy ID 183855
Linked level species

Family

Family in NCBI taxonomy Myrtaceae
ID 3931

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
C00036480 External link 512 Colosic acid
/ 2alpha-Hydroxyursolic acid
CHEMBL391533
CHEMBL237535
CHEMBL391534
CHEMBL574993
C113861
17 / 7 / 6 No. 13 No. 51
C00037978 External link 512 Ursolic acid lactone
CHEMBL1590724
2 / 4 / 4 No. 23 No. 51
C00029633 External link 512 Ursolic acid
/ Acetylursolic acid
CHEMBL55086
CHEMBL410525
4 / 2 / 2 No. 177

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

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 DISEASE (12)

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)