Species

KNApSAcK Entry

Organism name Streptomyces sp.KSC-5791
Genus Streptomyces
Family Streptomycetaceae
Kingdom Bacteria

NCBI taxonomy

Entry

Linked NCBI taxonomy name Streptomyces
Linked NCBI taxonomy ID 1883
Linked level genus

Family

Family in NCBI taxonomy Streptomycetaceae
ID 2062

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Bacteria
ID 2

Plant class

Plant class
ID

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
C00002037 External link 512 DMDP
/ (+)-2,5-Dideoxy-2,5-imino-D-mannitol
/ 2R,5R-Dihydroxymethyl-3R,4R-dihydroxy-pyrrolidine
CHEMBL10437
CHEMBL312653
CHEMBL121093
CHEMBL259905
CHEMBL405957
CHEMBL469844
CHEMBL2008021
C043121
8 / 10 / 8 No. 667

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00002037 6 / 4
Q14697 Neutral alpha-glucosidase AB Enzyme C00002037 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002037 1 / 1
Q9H227 Cytosolic beta-glucosidase Enzyme C00002037 0 / 0
P35573 Glycogen debranching enzyme Enzyme C00002037 1 / 1
P04066 Tissue alpha-L-fucosidase Enzyme C00002037 1 / 2
P06280 Alpha-galactosidase A Enzyme C00002037 1 / 1
O43451 Maltase-glucoamylase, intestinal Hydrolase C00002037 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#301500 Fabry disease P06280
#230000 Fucosidosis P04066
#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
#232300 Glycogen storage disease ii P10253
#232400 Glycogen storage disease iii P35573
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (8)

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)
H00141 Fucosidosis P04066 (related)
H00422 Glycoproteinoses P04066 (related)
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
P35573 (related)