Species

KNApSAcK Entry

Organism name Callicarpa formosana
Genus Callicarpa
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Callicarpa formosana
Linked NCBI taxonomy ID 886264
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

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
C00004655 External link 512 Quercetin pentamethyl ether
/ 3,5,7,3',4'-Pentamethoxyflavone
CHEMBL19032
16 / 10 / 12 No. 8 No. 15
C00029633 External link 512 Ursolic acid
/ Acetylursolic acid
CHEMBL55086
CHEMBL410525
4 / 2 / 2 No. 177

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P33527 Multidrug resistance-associated protein 1 drugs C00004655 0 / 0
P06746 DNA polymerase beta Enzyme C00029633 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00004655 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00004655 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00004655 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00004655 2 / 2
P39748 Flap endonuclease 1 Enzyme C00004655 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00004655 0 / 0
Q12791 Calcium-activated potassium channel subunit alpha-1 KCNM, KCa1.x C00004655 1 / 1
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00029633 2 / 2
P28482 Mitogen-activated protein kinase 1 Erk C00004655 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004655 2 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004655 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00004655 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00029633 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004655 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00029633 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00004655 1 / 1
O00255 Menin Unclassified protein C00004655 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004655 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

OMIM preferred title UniProt
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614490 Blood group, junior system; jr Q9UNQ0
#609446 Generalized epilepsy and paroxysmal dyskinesia; gepd Q12791
#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
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0

KEGG DISEASE (14)

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)
H00036 Osteosarcoma P08684 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (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)
H01258 Generalized epilepsy and paroxysmal dyskinesia (GEPD) Q12791 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)