Protein Name: Hydroxymethylglutaryl-CoA synthase, mitochondrial
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UniprotKB/SwissProt ID: HMCS2_HUMAN (P54868)
Gene Name: HMGCS2
Organism: Homo sapiens (Human).
Function: This enzyme condenses acetyl-CoA with acetoacetyl-CoA to form HMG-CoA, which is the substrate for HMG-CoA reductase.
Other Modifications: View all modification sites in dbPTM
Protein Subcellular Localization: Mitochondrion.
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PDB :
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Protein disease:
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| Disease database |
Database Entry |
Disease information | | HPRD | 02580 | HMG-CoA synthase deficiency |
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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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