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    <!-- http://purl.obolibrary.org/obo/UPa_UPA00058 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/UPa_UPA00058">
        <rdfs:label>(R)-mevalonate biosynthesis</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/UPa_UPA00415"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/UPa_UPA00497"/>
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        <oboInOwl:hasDbXref>KEGG:map00362</oboInOwl:hasDbXref>
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        <oboInOwl:hasDbXref>KEGG:map00072</oboInOwl:hasDbXref>
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        <ns3:IAO_0000115>Biosynthesis of mevalonic acid, a six-carbon metabolic intermediate. In eukaryotes, it arises from linkage of two acetyl-CoAs in the mitochondrion to form acetaoacetyl-CoA (4 carbons), followed by addition of another acetyl group from a third acetyl-CoA to give 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA). This latter compound is reduced by HMG-CoA reductase in the endoplasmic reticulum, using two NADPHs, with coincident loss of CoASH. HMG-CoA reductase is the most important regulatory enzyme for the cholesterol biosynthetic pathway and other isoprenoids/terpenoids. HMG-CoA reductase is a target for drugs that attempt to lower cholesterol levels in the body. One such drug is lovastatin, which inhibits the enzyme and stops endogenous synthesis of cholesterol.</ns3:IAO_0000115>
        <oboInOwl:hasExactSynonym>mevalonic acid biosynthesis</oboInOwl:hasExactSynonym>
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        <rdfs:label>metabolic intermediate biosynthesis</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/UPa_UPA00497 -->

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        <rdfs:label>(R)-mevalonate metabolism</rdfs:label>
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