Species

KNApSAcK Entry

Organism name Corymbia tessellaris
Genus Corymbia
Family Myrtaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Corymbia tessellaris
Linked NCBI taxonomy ID 34330
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 (1)

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
C00002896 External link 512 Piceid
/ Resveratrol 3-O-beta-glucopyranoside
/ 3,3',4,5'-Tetrahydroxystilbene 3-O-beta-D-glucopyranoside
CHEMBL142652
CHEMBL509386
CHEMBL597338
CHEMBL1990895
7 / 6 / 4 No. 36 No. 13

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00002896 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002896 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002896 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002896 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002896 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002896 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002896 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (4)

KEGG name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)