Species

KNApSAcK Entry

Organism name Quercus miyagii
Genus Quercus
Family Fagaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Quercus miyagii
Linked NCBI taxonomy ID 103491
Linked level species

Family

Family in NCBI taxonomy Fagaceae
ID 3503

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (10)

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
C00008841 External link 512 Catechin 3-O-beta-D-glucopyranoside
No. 12 No. 14
C00008843 External link 512 Catechin 3-O-alpha-L-rhamnoside
No. 12 No. 14
C00009071 External link 512 Procyanidin B3
/ Catechin-(4alpha->8)-catechin
CHEMBL38714
CHEMBL81753
CHEMBL504937
CHEMBL501490
CHEMBL447373
CHEMBL1253314
CHEMBL1590914
20 / 7 / 8 No. 16 No. 19
C00009070 External link 512 Procyanidin B6
/ Catechin-(4alpha->6)-catechin
CHEMBL506487
CHEMBL502984
CHEMBL451115
No. 16 No. 19
C00009074 External link 512 Procyanidin B7
/ Catechin-(4beta->6)-catechin
CHEMBL506487
CHEMBL502984
CHEMBL451115
No. 16 No. 19
C00009111 External link 512 Prodelphinidin C
No. 16 No. 19
C00009075 External link 512 Procyanidin B1
/ Epicatechin-(4beta->8)-catechin
CHEMBL38714
CHEMBL81753
CHEMBL504937
CHEMBL501490
CHEMBL447373
CHEMBL1253314
CHEMBL1590914
C479579
20 / 7 / 8 No. 16 No. 19
C00009095 External link 512 Procyanidin C4
CHEMBL290632
13 / 5 / 6 No. 29 No. 19
C00009200 External link 512 3-O-alpha-L-Rhamnopyranosylcatechin-(4alpha->8)-catechin
No. 341
C00009203 External link 512 Catechin-(4alpha->8)-catechin-3-O-rhamnopyranoside
No. 341

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q15139 Serine/threonine-protein kinase D1 Pkd C00009071 C00009075 C00009095 0 / 0
P41743 Protein kinase C iota type Iota C00009071 C00009075 C00009095 0 / 0
P24723 Protein kinase C eta type Eta C00009071 C00009075 C00009095 1 / 0
P05771 Protein kinase C beta type Alpha C00009071 C00009075 C00009095 0 / 0
P05129 Protein kinase C gamma type Alpha C00009071 C00009075 C00009095 1 / 1
Q05655 Protein kinase C delta type Delta C00009071 C00009075 C00009095 0 / 0
P17252 Protein kinase C alpha type Alpha C00009071 C00009075 C00009095 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00009071 C00009075 C00009095 0 / 0
Q02156 Protein kinase C epsilon type Eta C00009071 C00009075 C00009095 0 / 0
Q04759 Protein kinase C theta type Delta C00009071 C00009075 C00009095 0 / 1
Q05513 Protein kinase C zeta type Iota C00009071 C00009075 C00009095 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00009071 C00009075 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00009071 C00009075 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00009071 C00009075 0 / 0
P23467 Receptor-type tyrosine-protein phosphatase beta Receptor tyrosine-protein phosphatase C00009071 C00009075 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00009071 C00009075 3 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00009071 C00009075 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00009071 C00009075 0 / 0
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00009071 C00009075 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00009071 C00009075 1 / 0
P14780 Matrix metalloproteinase-9 M10A C00009095 2 / 2
P08253 72 kDa type IV collagenase M10A C00009095 1 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#603932 Intervertebral disc disease; idd P14780
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#605361 Spinocerebellar ataxia 14; sca14 P05129
#601367 Stroke, ischemic P24723

KEGG DISEASE (12)

KEGG name UniProt
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00028 Choriocarcinoma P08253 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00408 Type I diabetes mellitus Q04759 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)