Species

KNApSAcK Entry

Organism name Pinus sativum
Genus Pinus
Family Pinaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pinaceae
Linked NCBI taxonomy ID 3318
Linked level family

Family

Family in NCBI taxonomy Pinaceae
ID 3318

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Metabolite list (3)

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
C00005446 External link 512 Quercetin 3-sophorotrioside
CHEMBL1413586
13 / 7 / 5 No. 5 No. 15
C00000299 External link 512 GA98
/ Gibberellin A98
No. 40 No. 41
C00000060 External link 512 GA60
/ Gibberellin A60
No. 40 No. 41

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00005446 0 / 0
P06746 DNA polymerase beta Enzyme C00005446 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005446 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005446 1 / 0
Q9Y253 DNA polymerase eta Enzyme C00005446 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00005446 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00005446 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005446 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00005446 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00005446 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00005446 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00005446 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005446 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (5)

KEGG name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)