Streptomyces hygroscopicus subsp. limoneus (IFO 12703, ATCC 21431, FERM-P 468)
Species
KNApSAcK Entry
| Organism name | Streptomyces hygroscopicus subsp. limoneus (IFO 12703, ATCC 21431, FERM-P 468) |
|---|---|
| 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 (3)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00017741
|
Deoxyvalidamine
|
C047788
|
No. 2218 |
|
||||
|
C00017740
|
2-epi-Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
4 / 8 / 6 | No. 4033 |
|
|||
|
C00017739
|
1-epi-Valiolamine
|
CHEMBL9216
CHEMBL223096 CHEMBL222396 |
4 / 8 / 6 | No. 4033 |
|
Human Protein / Gene in interactions
4 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00017739 C00017740 | 6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00017739 C00017740 | 1 / 1 |
| P14410 | Sucrase-isomaltase, intestinal | Enzyme | C00017739 C00017740 | 1 / 1 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00017739 C00017740 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (8)
| 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 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)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|