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    <!-- http://purl.obolibrary.org/obo/MOD_00918 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MOD_00918">
        <rdfs:label>modified L-tryptophan residue</rdfs:label>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MOD_00962 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MOD_00962">
        <rdfs:label>2&#39;,3&#39;-dihydrotryptophan</rdfs:label>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MOD_00918"/>
        <rdfs:subClassOf rdf:resource="http://purl.obolibrary.org/obo/MOD_01473"/>
        <ns2:MassMono_ rdf:datatype="http://www.w3.org/2001/XMLSchema#float">188.0949554443359375</ns2:MassMono_>
        <ns2:MassAvg_ rdf:datatype="http://www.w3.org/2001/XMLSchema#float">188.2299957275390625</ns2:MassAvg_>
        <ns2:DiffMono_ rdf:datatype="http://www.w3.org/2001/XMLSchema#float">2.0156500339508056641</ns2:DiffMono_>
        <ns2:DiffAvg_ rdf:datatype="http://www.w3.org/2001/XMLSchema#float">2.0199999809265136719</ns2:DiffAvg_>
        <ns2:IAO_0000115>A protein modification that by reducing the indole ring system of tryptophan to indoline effectively converts an L-tryptophan residue to 2&#39;,3&#39;-dihydrotryptophan.</ns2:IAO_0000115>
        <ns2:Origin_>W</ns2:Origin_>
        <ns2:DiffFormula_>H 2</ns2:DiffFormula_>
        <oboInOwl:id>MOD:00962</oboInOwl:id>
        <ns2:Formula_>C 11 H 12 N 2 O 1</ns2:Formula_>
        <ns2:TermSpec_>none</ns2:TermSpec_>
        <oboInOwl:hasOBONamespace>PSI-MOD</oboInOwl:hasOBONamespace>
        <ns2:Source_>artifact</ns2:Source_>
        <rdfs:comment>From DeltaMass: References:1. Pearson,D.A., Blanchette,M., Baker,M.L. and Guindon,C.A. (1989) Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking ofprotecting groups in peptide synthesis. Tetrahedron Lett., 30(21), 2739-2742 Notes: Reduction of indole double bond of Trp which occurs when triethylsilane (TES) is used as a scavenger and Trp is incorporated without protection of indole nitrogen [1]. This side reaction is likely to be accompanied by oxidation of indoline ring with formation of intensively colored peptide by-products. Triisopropylsilane (TIPS) does not give this side reaction. See structure at http://www.abrf.org/images/misc/dmass2.gif. [However, the pictured indoline structure is incorrect - JSG].</rdfs:comment>
    </Class>
    


    <!-- http://purl.obolibrary.org/obo/MOD_01473 -->

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        <rdfs:label>hydrogenated residue</rdfs:label>
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