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    <!-- http://purl.obolibrary.org/obo/HINO_0011418 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0011418">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">PathwayStep2754</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HINO_0016364 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0016364">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Amino Acid conjugation</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/INO_0000021"/>
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            <Restriction>
                <onProperty rdf:resource="http://www.obofoundry.org/ro/ro.owl#has_part"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HINO_0016366"/>
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                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/NCBITaxon_9606"/>
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                <onProperty rdf:resource="http://www.biopax.org/release/biopax-level3.owl#pathwayOrder"/>
                <someValuesFrom rdf:resource="http://purl.obolibrary.org/obo/HINO_0011418"/>
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        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Authored: Jassal, B, 2005-03-10 15:37:26</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:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">GENE ONTOLOGYGO:0006805</rdfs:seeAlso>
        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Reactome Database ID Release 43156587</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_6971</rdfs:seeAlso>
        <rdfs:comment rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Xenobiotics that contain either a carboxylic group or an aromatic hydroxylamine group are possible substrates for amino acid conjugation. Xenobiotics with a &lt;i&gt;carboxylic group&lt;/i&gt; conjugate with an &lt;i&gt;amino group&lt;/i&gt; of amino acids such as glycine, taurine and glutamine. The &lt;i&gt;hydroxylamine group&lt;/i&gt; conjugates with the &lt;i&gt;carboxylic group&lt;/i&gt; of amino acids such as proline and serine. The amino acid is first activated by an aminoacyl-tRNA-synthetase which then reacts with the hydroxylamine group to form a reactive N-ester. N-esters can degrade to form electrophilic nitrenium (R-N&lt;sup&gt;+&lt;/sup&gt;-R&#39;) and carbonium (R-C&lt;sup&gt;+&lt;/sup&gt;H&lt;sub&gt;2&lt;/sub&gt;) ions. The pyrolysis product of tryptophan, an N-hydroxy intermediate, can potentially form these reactive electrophilic ions.</rdfs:comment>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/HINO_0016366 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/HINO_0016366">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Conjugation of carboxylic acids</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/INO_0000021 -->

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    <!-- http://purl.obolibrary.org/obo/NCBITaxon_9606 -->

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