Species

KNApSAcK Entry

Organism name Malus pumila
Genus Malus
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Malus pumila
Linked NCBI taxonomy ID 283210
Linked level species

Family

Family in NCBI taxonomy Rosaceae
ID 3745

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

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
C00006651 External link 512 Cyanidin 3-xyloside
No. 2 No. 15
C00009090 External link 512 Epicatechin-(4beta->8)-epicatechin-(4beta->6)-epicatechin
CHEMBL592329
2 / 3 / 4 No. 29 No. 19
C00000100 External link 512 IAA
/ Indole-3-acetic acid
CHEMBL82411
C030737
3 / 0 / 0 2 / 1 No. 1432 No. 4
C00000134 External link 512 (s)-(+)-Abscisic acid
/ 2,4-Pentadienoic acid
CHEMBL288040
CHEMBL379808
CHEMBL1318134
CHEMBL1469719
CHEMBL1741460
CHEMBL1965138
D000040
10 / 9 / 10 No. 1435 No. 38
C00000101 External link 512 IAA methyl ester
/ Methyl indole-3-acetate
No. 4225
C00000175 External link 512 Ethylene
CHEMBL117822
C036216
No. 8854

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000134 1 / 0
Q16773 Kynurenine--oxoglutarate transaminase 1 Enzyme C00000100 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00009090 2 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00000134 3 / 2
P02768 Serum albumin Secreted protein C00000100 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000134 0 / 1
P10145 Interleukin-8 Secreted protein C00000134 0 / 0
Q9HBH1 Peptide deformylase, mitochondrial Enzyme C00000100 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000134 0 / 0
P08253 72 kDa type IV collagenase M10A C00009090 1 / 3
P03372 Estrogen receptor NR3A1 C00000134 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000134 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000134 0 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000134 0 / 0
P10275 Androgen receptor NR3C4 C00000134 3 / 4

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00000100
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00000100

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#603932 Intervertebral disc disease; idd P14780
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (14)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00028 Choriocarcinoma P08253 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H01205 Coumarin resistance P11712 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00000100