PCIDB

Prunus dulcis var. amara

Species

KNApSAcK Entry

Organism name Prunus dulcis var. amara
Genus Prunus
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Prunus dulcis var. amara
Linked NCBI taxonomy ID 3756
Linked level varietas

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 (1)

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
C00001426 External link 512 Phenethylamine
CHEMBL610
C029261
8 / 6 / 2 6 / 5 No. 885

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00001426 4 / 1
P08183 Multidrug resistance protein 1 drug C00001426 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001426 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001426 0 / 0
Q16853 Membrane primary amine oxidase Enzyme C00001426 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001426 0 / 0
Q96RJ0 Trace amine-associated receptor 1 Trace amine receptor C00001426 0 / 0
P07477 Trypsin-1 S1A C00001426 1 / 1

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4129 MAOB monoamine oxidase B (EC:1.4.3.4) C00001426
6570 SLC18A1, CGAT, VAT1, VMAT1 solute carrier family 18 (vesicular monoamine transporter), member 1 C00001426
6530 SLC6A2, NAT1, NET, NET1, SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 2 C00001426
6531 SLC6A3, DAT, DAT1, PKDYS solute carrier family 6 (neurotransmitter transporter), member 3 C00001426
6532 SLC6A4, 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT solute carrier family 6 (neurotransmitter transporter), member 4 C00001426
134864 TAAR1, RP11-295F4.9, TA1, TAR1, TRAR1 trace amine associated receptor 1 C00001426

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#612244 Inflammatory bowel disease 13; ibd13 P08183
#167800 Pancreatitis, hereditary; pctt P07477
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637

KEGG DISEASE (2)

KEGG name UniProt
H00933 Hereditary pancreatitis P07477 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002375 Catalepsy C00001426
D004409 Dyskinesia, Drug-Induced C00001426
D006948 Hyperkinesis C00001426
D015878 Mydriasis C00001426
D019954 Neurobehavioral Manifestations C00001426