Species

KNApSAcK Entry

Organism name Lolium perenne L.
Genus Lolium
Family Poaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lolium perenne
Linked NCBI taxonomy ID 4522
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 (7)

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
C00036257 External link 512 25-Methylcastasterone
No. 68 No. 11
C00023584 External link 512 beta-Paxitriol
No. 819
C00023583 External link 512 alpha-Paxitriol
No. 819
C00023582 External link 512 Paxilline
CHEMBL410063
CHEMBL1372110
CHEMBL1396845
C048220
27 / 25 / 19 5 / 0 No. 819
C00023578 External link 512 Lolitriol
No. 2224
C00023577 External link 512 Lolitrem E
/ Lolitrem C
No. 2224
C00019144 External link 512 Loliolide
/ (-)-Loliolide
CHEMBL227113
CHEMBL446471
C030425
1 / 2 / 2 No. 2667

Human Protein / Gene in interactions

28 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00023582 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00023582 0 / 0
Q99700 Ataxin-2 Unclassified protein C00023582 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00023582 2 / 0
P04062 Glucosylceramidase Enzyme C00023582 6 / 4
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00023582 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00023582 0 / 1
P42858 Huntingtin Unclassified protein C00023582 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00023582 2 / 0
O75496 Geminin Unclassified protein C00023582 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00023582 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00023582 1 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00023582 0 / 0
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00023582 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00019144 2 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00023582 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00023582 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00023582 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00023582 0 / 1
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00023582 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00023582 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00023582 4 / 3
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00023582 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00023582 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00023582 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00023582 0 / 0
O00255 Menin Unclassified protein C00023582 2 / 5
Q13148 TAR DNA-binding protein 43 Unclassified protein C00023582 1 / 1

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00023582
1385 CREB1, CREB cAMP responsive element binding protein 1 C00023582
10062 NR1H3, LXR-a, LXRA, RLD-1 nuclear receptor subfamily 1, group H, member 3 C00023582
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00023582
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00023582

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (27)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#143100 Huntington disease; hd P42858
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (21)

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)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00059 Huntington's disease (HD) P42858 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)