Organism name | Streptomyces sp.KSC-5791 |
---|---|
Genus | Streptomyces |
Family | Streptomycetaceae |
Kingdom | Bacteria |
Linked NCBI taxonomy name | Streptomyces |
---|---|
Linked NCBI taxonomy ID | 1883 |
Linked level | genus |
Family in NCBI taxonomy | Streptomycetaceae |
---|---|
ID | 2062 |
Kingdom (Superkingdom) in NCBI taxonomy | Bacteria |
---|---|
ID | 2 |
Plant class | |
---|---|
ID |
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
![]() |
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 |
![]() |
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 |
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 | 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) |