Species

KNApSAcK Entry

Organism name Phalaris arundinacea
Genus Phalaris
Family Poaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Phalaris arundinacea
Linked NCBI taxonomy ID 96050
Linked level species

Family

Family in NCBI taxonomy Poaceae
ID 4479

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

Metabolite list (9)

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
C00006799 External link 512 Cyanidin 3-(3'',6''-dimalonylglucoside)
No. 2 No. 15
C00006796 External link 512 Cyanidin 3-(6''-malonylglucoside)
/ Cyanidin-3-O-(6-O-malonyl-beta-D-glucopyranoside)
CHEMBL1173160
No. 2 No. 15
C00006681 External link 512 Oxycoccicyanin
/ Peonidin 3-O-beta-D-glucopyranoside
CHEMBL1784263
No. 2 No. 15
C00002374 External link 512 Chrysanthemin
/ Cyanidin 3-O-glucoside
CHEMBL257839
CHEMBL1197952
C114438
1 / 0 / 1 No. 2 No. 15
C00006679 External link 512 Peonidin 3-arabinoside
No. 2 No. 15
C00006650 External link 512 Cyanidin 3-arabinoside
No. 2 No. 15
C00001417 External link 512 Cactine
/ Anhalin
/ Anhaline
/ Hordenine
CHEMBL505789
C007964
1 / 0 / 0 No. 936 No. 6
C00001420 External link 512 O-Methylbufotenine
/ N,N-Dimethyl-5-methoxytryptamine
/ 5-Methoxy-N,N-dimethyltryptamine
CHEMBL7257
14 / 3 / 3 No. 1385 No. 4
C00001411 External link 512 Gramine
CHEMBL254348
C007884
13 / 11 / 15 No. 1385 No. 4

Human Protein / Gene in interactions

24 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001411 C00001420 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001411 C00001420 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001411 C00001420 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001411 C00001420 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001411 C00001420 0 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001411 3 / 3
P28222 5-hydroxytryptamine receptor 1B Serotonin receptor C00001420 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001411 0 / 0
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001420 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001420 0 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00001420 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00001411 3 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00001420 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001420 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001420 0 / 0
P28907 ADP-ribosyl cyclase 1 Enzyme C00002374 0 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001411 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001411 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00001420 1 / 0
P28221 5-hydroxytryptamine receptor 1D Serotonin receptor C00001420 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001411 0 / 0
O00255 Menin Unclassified protein C00001411 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001411 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001417 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

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
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#614674 Periodic fever, menstrual cycle-dependent P08908

KEGG DISEASE (16)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00005 Chronic lymphocytic leukemia (CLL) P28907 (marker)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)