Hexokinase-1

Summary
GlyCosmos Lectin
GL_002536
Lectin Name Aliases
  • Brain form hexokinase
  • HK I
  • Hexokinase type I
  • Hexokinase-A
Organism
Homo sapiens (human)
UniProt
P19367
Annotation
Keyword
3D-structure ATP-binding Acetylation Allosteric enzyme Alternative splicing Charcot-Marie-Tooth disease Cytoplasm Direct protein sequencing Disease variant Glycolysis Hereditary hemolytic anemia Inflammatory response Innate immunity Intellectual disability Kinase Mitochondrion outer membrane Neurodegeneration Phosphoprotein Proteomics identification Reference proteome Repeat Retinitis pigmentosa
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Pathway
Displaying all 3 entries
Pathway Name Organism
Defective HK1 causes hexokinase deficiency (HK deficiency) Homo sapiens
Glycolysis Homo sapiens
Synthesis of GDP-mannose Homo sapiens

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026