Protein Name: Hexokinase-1
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UniprotKB/SwissProt ID: HXK1_HUMAN (P19367)
Gene Name: HK1
Organism: Homo sapiens (Human).
Function:
Other Modifications: View all modification sites in dbPTM
Protein Subcellular Localization: Mitochondrion outer membrane. Note=Its hydrophobic N-terminal sequence may be involved in membrane binding.
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PDB :
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Protein disease:
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| Disease database |
Database Entry |
Disease information | | KEGG | H00664 | Anemia due to disorders of glycolytic enzymes, including: Hexokinase (HK) deficiency; Phosphoglycera | | OMIM | 142600 | HEXOKINASE 1; HK1 | | OMIM | 235700 | HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY | | OMIM | 605285 | NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE ;;HEREDITARY MOTOR AND SENSORY NEUROPAT | | HPRD | 00809 | Hexokinase deficiency hemolytic anemia |
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Network with metabolic pathway:
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Graphical Visualization of S-nitrosylation Sites:
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| Overview of Protein S-nitrosylation Sites with Functional and Structural Information |  |
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