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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Hematopoietic prostaglandin D synthase
Summary
- UniProt ID
- O60760
- Gene Symbol
-
- HPGDS
- GSTS
- PGDS
- PTGDS2
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- O60760
- PubChem
- O60760
- SwissLipids
- The Human Metabolome Database
- HMDBP01575
- The O-GlcNAc Database
- O60760
- O-GlcNAcAtlas
- O60760
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Cytoplasm
- Isomerase
- Magnesium
- Metal-binding
- Prostaglandin biosynthesis
- Reference proteome
- Transferase
- Gene Ontology (GO)
| GO Term |
|---|
| cytoplasm |
| intracellular membrane-bounded organelle |
| cytosol |
| nucleoplasm |
| GO Term |
|---|
| protein homodimerization activity |
| magnesium ion binding |
| glutathione transferase activity |
| prostaglandin-D synthase activity |
| calcium ion binding |
Sequence
MPNYKLTYFNMRGRAEIIRYIFAYLDIQYEDHRIEQADWPEIKSTLPFGKIPILEVDGLTLHQSLAIARYLTKNTDLAGNTEMEQCHVDAIVDTLDDFMSCFPWAEKKQDVKEQMFNELLTYNAPHLMQDLDTYLGGREWLIGNSVTWADFYWEICSTTLLVFKPDLLDNHPRLVTLRKKVQAIPAVANWIKRRPQTKL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 7 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Glutathione conjugation | Homo sapiens |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | |
| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | |
| DOID:0110300 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1A | |
| DOID:0110301 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1B | |
| DOID:0110302 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1C | |
| DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H | |
| DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 | |
| DOID:0110305 | autosomal dominant limb-girdle muscular dystrophy type 1 | |
| DOID:0110306 | autosomal dominant limb-girdle muscular dystrophy type 3 | |
| DOID:0110741 | type 1 diabetes mellitus 2 |
