Species

KNApSAcK Entry

Organism name Jasonia candicans
Genus Jasonia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Jasonia
Linked NCBI taxonomy ID 56532
Linked level genus

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 (2)

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
C00004602 External link 512 6-Hydroxykaempferol 3,5,7-trimethyl ether
No. 3 No. 15
C00004703 External link 512 Quercetagetin 3,5,7,4'-tetramethyl ether
CHEMBL76887
11 / 11 / 11 No. 8 No. 15

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00004703 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00004703 1 / 0
P39748 Flap endonuclease 1 Enzyme C00004703 0 / 0
O75496 Geminin Unclassified protein C00004703 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00004703 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00004703 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00004703 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00004703 1 / 0
O00255 Menin Unclassified protein C00004703 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004703 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00004703 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (11)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)