Species

KNApSAcK Entry

Organism name Jasminum urophyllum
Genus Jasminum
Family Oleaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Jasminum
Linked NCBI taxonomy ID 4147
Linked level genus

Family

Family in NCBI taxonomy Oleaceae
ID 4144

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (5)

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
C00050135 External link 512 Jasuroside C
/ (-)-Jasuroside C
CHEMBL1482441
10 / 7 / 5 No. 472
C00050133 External link 512 Jasuroside A
/ (-)-Jasuroside A
No. 472
C00050136 External link 512 Jasuroside D
/ (-)-Jasuroside D
No. 2713
C00050134 External link 512 Jasuroside B
/ (-)-Jasuroside B
No. 2713
C00044206 External link 512 Jasurolignoside
/ (-)-Jasurolignoside
No. 8108

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00050135 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00050135 1 / 1
O75496 Geminin Unclassified protein C00050135 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00050135 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00050135 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00050135 1 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00050135 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00050135 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00050135 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00050135 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#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)