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    <!-- http://purl.obolibrary.org/obo/HINO_0011391 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PathwayStep2743</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0011393 -->

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    <!-- http://purl.obolibrary.org/obo/HINO_0011395 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PathwayStep2741</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/HINO_0016336 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0016336">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Glutathione conjugation</rdfs:label>
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        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Authored: Jassal, B, 2004-11-30 11:49:48</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Edited: Jassal, B, 2008-05-19 12:57:01</rdfs:comment>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Glutathione S-Transferases (GSTs; EC 2.5.1.18) are another major set of phase II conjugation enzymes. They can be found in the cytosol as well as being microsomal membrane-bound. Cytosolic GSTs are encoded by at least 5 gene families (alpha, mu, pi, theta  and zeta GST) whereas membrane-bound enzymes are encoded by single genes. Soluble GSTs are homo- or hetero-dimeric enzymes (approximately 25KDa subunits) which can act on a wide range of endogenous and exogenous  electrophiles. GSTs mediate conjugation using glutathione (GSH), a tripeptide synthesized from its precursor amino acids gamma-glutamate, cysteine and glycine. A generalized reaction is&lt;p&gt;&lt;b&gt;RX + GSH -&gt; HX + GSR&lt;/b&gt;&lt;/p&gt;Glutathione conjugates are excreted in bile and converted to cysteine and mercapturic acid conjugates in the intestine and kidneys. GSH is the major, low molecular weight, non-protein thiol synthesized &lt;i&gt;de novo&lt;/i&gt; in mammalian cells. As well as taking part in conjugation reactions, GSH also has antioxidant ability and can metabolize endogenous and exogenous compounds. The nucleophilic GSH attacks the electrophilic substrate forming a thioether bond between the cysteine residue of GSH and the electrophile. The result is generally a less reactive and more water-soluble conjugate that can be easily excreted. In some cases, GSTs can activate compounds to reactive species such as certain haloalkanes and haloalkenes. Substrates for GSTs include epoxides, alkenes and compounds with electrophilic carbon, sulfur or nitrogen centres. There are two types of conjugation reaction with glutathione: &lt;i&gt;displacement reactions&lt;/i&gt; where glutathione displaces an electron-withdrawing group and &lt;i&gt;addition reactions&lt;/i&gt; where glutathione is added to activated double bond structures or strained ring systems.</rdfs:comment>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome Database ID Release 43156590</rdfs:seeAlso>
        <ns3:IAO_0000119 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome, http://www.reactome.org</ns3:IAO_0000119>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">ReactomeREACT_6926</rdfs:seeAlso>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reviewed: D&#39;Eustachio, P, 2011-05-23</rdfs:comment>
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    <!-- http://purl.obolibrary.org/obo/HINO_0025139 -->

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    <!-- http://purl.obolibrary.org/obo/HINO_0025140 -->

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    <!-- http://purl.obolibrary.org/obo/INO_0000021 -->

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