| 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)
|