Organism name | Streptomyces hygroscopicus subsp. limoneus |
---|---|
Genus | Streptomyces |
Family | Streptomycetaceae |
Kingdom | Bacteria |
Linked NCBI taxonomy name | Streptomyces hygroscopicus subsp. limoneus |
---|---|
Linked NCBI taxonomy ID | 264445 |
Linked level | subspecies |
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 |
---|---|---|---|---|---|---|---|---|
C00017025
![]() |
Validamycin H
|
C066094
|
No. 772 |
![]() |
||||
C00017813
![]() |
Validamycin G
|
No. 772 |
![]() |
|||||
C00018831
![]() |
Validamycin D
|
No. 772 |
![]() |
|||||
C00018830
![]() |
Validamycin C
|
No. 772 |
![]() |
|||||
C00018832
![]() |
Validamycin E
|
No. 772 |
![]() |
|||||
C00018608
![]() |
Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
C043270
|
4 / 8 / 6 | No. 4033 |
![]() |
||
C00017814
![]() |
Validoxylamine G
/ (+)-Validoxylamine G |
C050693
|
No. 5783 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P04062 | Glucosylceramidase | Enzyme | C00018608 | 6 / 4 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00018608 | 1 / 1 |
P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00018608 | 1 / 1 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00018608 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#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
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|