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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Hexokinase-1
Summary
- Organism
- Homo sapiens (human)
External Links
- UniProt
- P19367
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Allosteric enzyme
- Alternative splicing
- Charcot-Marie-Tooth disease
- Cytoplasm
- Direct protein sequencing
- Disease variant
- Glycolysis
- Inflammatory response
- Innate immunity
- Intellectual disability
- Kinase
- Mitochondrion outer membrane
- Neurodegeneration
- Phosphoprotein
- Reference proteome
- Repeat
- Retinitis pigmentosa
- Gene Ontology (GO)
| GO Term |
|---|
| cytosol |
| mitochondrion |
| mitochondrial outer membrane |
| membrane raft |
| GO Term |
|---|
| peptidoglycan binding |
| hexokinase activity |
| glucosamine kinase activity |
| ATP binding |
| glucokinase activity |
| glucose binding |
| fructokinase activity |
| mannokinase activity |
Pathway
| Pathway Name | Organism |
|---|---|
| Defective HK1 causes hexokinase deficiency (HK deficiency) | Homo sapiens |
| Glycolysis | Homo sapiens |
