Species

KNApSAcK Entry

Organism name Liquidambar formosana
Genus Liquidambar
Family Hamamelidaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Liquidambar formosana
Linked NCBI taxonomy ID 63359
Linked level species

Family

Family in NCBI taxonomy Altingiaceae
ID 91829

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (6)

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
C00005729 External link 512 Myricetin 3-glucoside
/ Myricetin 3-O-beta-D-glucoside
/ Myricetin 3-O-beta-D-glucopyranoside
CHEMBL462244
CHEMBL1221722
No. 2 No. 15
C00005138 External link 512 Astragalin
/ Kaempferol 3-glucoside
/ Kaempferol 3-O-beta-D-glucoside
/ Kaempferol 3-O-beta-D-glucopyranoside
CHEMBL233930
CHEMBL453290
CHEMBL1572115
C001579
10 / 6 / 7 0 / 1 No. 2 No. 15
C00005958 External link 512 Quercetin 3-(6''-galloylglucoside)
CHEMBL499432
No. 98
C00006040 External link 512 Myricetin 3-(6''-galloylglucoside)
No. 98
C00035330 External link 512 Isorugosin D
No. 126 No. 81
C00002910 External link 512 Casuarinin
CHEMBL79244
CHEMBL507387
11 / 2 / 2 No. 226 No. 81

Human Protein / Gene in interactions

21 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00005138 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005138 0 / 0
P07237 Protein disulfide-isomerase Enzyme C00005138 0 / 0
P15121 Aldose reductase Enzyme C00005138 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00005138 1 / 1
P14679 Tyrosinase Oxidoreductase C00005138 4 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00005138 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00005138 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005138 0 / 0
Q05513 Protein kinase C zeta type Iota C00002910 0 / 0
Q04759 Protein kinase C theta type Delta C00002910 0 / 1
Q02156 Protein kinase C epsilon type Eta C00002910 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00002910 0 / 0
P17252 Protein kinase C alpha type Alpha C00002910 0 / 0
Q05655 Protein kinase C delta type Delta C00002910 0 / 0
P05129 Protein kinase C gamma type Alpha C00002910 1 / 1
P05771 Protein kinase C beta type Alpha C00002910 0 / 0
P24723 Protein kinase C eta type Eta C00002910 1 / 0
P41743 Protein kinase C iota type Iota C00002910 0 / 0
Q15139 Serine/threonine-protein kinase D1 Pkd C00002910 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00005138 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#605361 Spinocerebellar ataxia 14; sca14 P05129
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601367 Stroke, ischemic P24723
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (8)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
Q99700 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00408 Type I diabetes mellitus Q04759 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003876 Dermatitis, Atopic C00005138