Species

KNApSAcK Entry

Organism name Camellia japonica
Genus Camellia
Family Theaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Camellia japonica
Linked NCBI taxonomy ID 4443
Linked level species

Family

Family in NCBI taxonomy Theaceae
ID 27065

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (24)

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
C00006650 External link 512 Cyanidin 3-arabinoside
No. 2 No. 15
C00029892 External link 512 Camelliasaponin C1
CHEMBL1991460
CHEMBL1995831
14 / 14 / 8 No. 4 No. 51
C00029895 External link 512 Camellioside B
CHEMBL1289022
CHEMBL2087221
No. 4 No. 51
C00003507 External link 512 Camellidin I
No. 4 No. 51
C00003508 External link 512 Camellidin II
No. 4 No. 51
C00029897 External link 512 Camellioside D
CHEMBL2087222
No. 4 No. 51
C00029896 External link 512 Camellioside C
/ (-)-Camellioside C
No. 4 No. 51
C00029891 External link 512 Camelliasaponin B2
No. 4 No. 51
C00029890 External link 512 Camelliasaponin B1
No. 4 No. 51
C00029889 External link 512 Camelliasaponin A2
No. 4 No. 51
C00029894 External link 512 Camellioside A
/ (-)-Camellioside A
CHEMBL1289020
No. 4 No. 51
C00029888 External link 512 Camelliasaponin A1
No. 4 No. 51
C00029893 External link 512 Camelliasaponin C2
/ (+)-Camelliasaponin C2
CHEMBL1991460
CHEMBL1995831
14 / 14 / 8 No. 4 No. 51
C00009071 External link 512 Procyanidin B3
/ Catechin-(4alpha->8)-catechin
CHEMBL38714
CHEMBL81753
CHEMBL504937
CHEMBL501490
CHEMBL447373
CHEMBL1253314
CHEMBL1590914
20 / 7 / 8 No. 16 No. 19
C00006800 External link 512 Hyacinthin
/ Cyanidin 3-(6-O-p-coumarylglucoside)
No. 30 No. 15
C00009329 External link 512 Camelliatannin F
C089878
No. 142
C00009330 External link 512 Camelliatannin G
C089879
No. 142
C00009362 External link 512 Camelliatannin B
No. 142
C00009333 External link 512 Camelliatannin E
No. 142
C00009332 External link 512 Camelliatannin C
No. 142
C00009361 External link 512 Camelliatannin A
No. 142
C00002938 External link 512 Tellimagrandin I
CHEMBL450376
C087926
7 / 0 No. 302 No. 81
C00000218 External link 512 Jasmonic acid
/ trans-Jasmonic acid
/ 3-Oxo-2-(2Z-pentenyl)cyclotentylacetic acid
CHEMBL445499
CHEMBL449572
C011006
4 / 1 / 0 No. 707 No. 70
C00000219 External link 512 Methyl jasmonate
CHEMBL184827
CHEMBL461150
CHEMBL2139332
C072239
No. 3198

Human Protein / Gene in interactions

38 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00029892 C00029893 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00029892 C00029893 1 / 0
Q99700 Ataxin-2 Unclassified protein C00029892 C00029893 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00029892 C00029893 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00029892 C00029893 2 / 3
O75164 Lysine-specific demethylase 4A Enzyme C00029892 C00029893 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00029892 C00029893 2 / 0
O75496 Geminin Unclassified protein C00029892 C00029893 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00029892 C00029893 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00029892 C00029893 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00029892 C00029893 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00029892 C00029893 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00029892 C00029893 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00029892 C00029893 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00009071 1 / 1
Q04828 Aldo-keto reductase family 1 member C1 Enzyme C00000218 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00009071 0 / 0
P23467 Receptor-type tyrosine-protein phosphatase beta Receptor tyrosine-protein phosphatase C00009071 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00009071 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00009071 3 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00009071 0 / 1
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00009071 0 / 0
P52895 Aldo-keto reductase family 1 member C2 Enzyme C00000218 1 / 0
P42330 Aldo-keto reductase family 1 member C3 Enzyme C00000218 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00009071 0 / 1
P17516 Aldo-keto reductase family 1 member C4 Enzyme C00000218 1 / 0
Q05513 Protein kinase C zeta type Iota C00009071 0 / 0
Q04759 Protein kinase C theta type Delta C00009071 0 / 1
Q02156 Protein kinase C epsilon type Eta C00009071 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00009071 0 / 0
P17252 Protein kinase C alpha type Alpha C00009071 0 / 0
Q05655 Protein kinase C delta type Delta C00009071 0 / 0
P05129 Protein kinase C gamma type Alpha C00009071 1 / 1
P05771 Protein kinase C beta type Alpha C00009071 0 / 0
P24723 Protein kinase C eta type Eta C00009071 1 / 0
P41743 Protein kinase C iota type Iota C00009071 0 / 0
Q15139 Serine/threonine-protein kinase D1 Pkd C00009071 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00009071 1 / 0

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
43 ACHE, ACEE, ARACHE, N-ACHE, YT acetylcholinesterase (EC:3.1.1.7) C00002938
2623 GATA1, ERYF1, GATA-1, GF-1, GF1, NF-E1, NFE1, XLANP, XLTDA, XLTT GATA binding protein 1 (globin transcription factor 1) C00002938
2624 GATA2, DCML, MONOMAC, NFE1B GATA binding protein 2 C00002938
2993 GYPA, CD235a, GPA, GPErik, GPSAT, HGpMiV, HGpMiXI, HGpSta(C), MN, MNS, PAS-2 glycophorin A (MNS blood group) C00002938
3145 HMBS, PBG-D, PBGD, PORC, UPS hydroxymethylbilane synthase (EC:2.5.1.61) C00002938
3690 ITGB3, BDPLT16, BDPLT2, CD61, GP3A, GPIIIa, GT integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) C00002938
4778 NFE2, NF-E2, p45 nuclear factor, erythroid 2 C00002938

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#614279 46,xy sex reversal 8; srxy8 P17516
P52895
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#605361 Spinocerebellar ataxia 14; sca14 P05129
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601367 Stroke, ischemic P24723
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (15)

KEGG name UniProt
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
Q99700 (related)
H00036 Osteosarcoma P08684 (marker)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)