Species

KNApSAcK Entry

Organism name Boenninghausenia spp.
Genus Boenninghausenia
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Boenninghausenia
Linked NCBI taxonomy ID 452762
Linked level genus

Family

Family in NCBI taxonomy Rutaceae
ID 23513

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
C00002456 External link 512 Chalepensin
CHEMBL1333931
C020740
7 / 8 / 6 No. 3930 No. 25

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00002456 6 / 4
P42858 Huntingtin Unclassified protein C00002456 1 / 1
O75496 Geminin Unclassified protein C00002456 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002456 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002456 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002456 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002456 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#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
#143100 Huntington disease; hd P42858
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (6)

KEGG name UniProt
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)
H00059 Huntington's disease (HD) P42858 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)