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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Glutamine synthetase
Summary
- UniProt ID
- P15104
- Gene Symbol
-
- GLUL
- GLNS
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Angiogenesis
- Cell membrane
- Cytoplasm
- Disease variant
- Ligase
- Magnesium
- Manganese
- Metal-binding
- Microsome
- Mitochondrion
- Palmitate
- Phosphoprotein
- Reference proteome
- Transferase
- Ubl conjugation
- Gene Ontology (GO)
| GO Term |
|---|
| nucleus |
| cytoplasm |
| plasma membrane |
| cell body |
| extracellular exosome |
| glial cell projection |
| mitochondrion |
| cytosol |
| endoplasmic reticulum |
| GO Term |
|---|
| ATP binding |
| metal ion binding |
| protein-cysteine S-palmitoyltransferase activity |
| identical protein binding |
| glutamine synthetase activity |
Sequence
MTTSASSHLNKGIKQVYMSLPQGEKVQAMYIWIDGTGEGLRCKTRTLDSEPKCVEELPEWNFDGSSTLQSEGSNSDMYLVPAAMFRDPFRKDPNKLVLCEVFKYNRRPAETNLRHTCKRIMDMVSNQHPWFGMEQEYTLMGTDGHPFGWPSNGFPGPQGPYYCGVGADRAYGRDIVEAHYRACLYAGVKIAGTNAEVMPAQWEFQIGPCEGISMGDHLWVARFILHRVCEDFGVIATFDPKPIPGNWNGAGCHTNFSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSASIRIPRTVGQEKKGYFEDRRPSANCDPFSVTEALIRTCLLNETGDEPFQYKN
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 142 |
|
|||
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Astrocytic Glutamate-Glutamine Uptake And Metabolism | Homo sapiens |
| Glutamate and glutamine metabolism | 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:0014667 | disease of metabolism | |
| DOID:0040085 | bacterial sepsis | |
| DOID:0050328 | congenital hypothyroidism | |
| DOID:0050486 | exanthem | |
| DOID:0050635 | alternating hemiplegia of childhood | |
| DOID:0050741 | alcohol dependence | |
| DOID:0050819 | obsolete Matthew-Wood syndrome | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060185 | Clostridium difficile colitis | |
| DOID:0060833 | Griscelli syndrome type 2 |
