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          <dc:contributor>Gerlt, John A.</dc:contributor>
          <dc:creator>Millikin, Cheri Lynn</dc:creator>
          <dc:date>2015-09-25T22:28:03Z</dc:date>
          <dc:date>2015-09-25T22:28:03Z</dc:date>
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          <dc:date>2005</dc:date>
          <dc:date>2005</dc:date>
          <dc:description>The dehydration of both D-mannonate, via syn-elimination, and D-altronate, via anti-elimination, is analogous to the stereochemical promiscuity engineered into the GlucD active site. The redesign of GlucD and the characterization of RspA illustrate the same type of promiscuity:  syn and anti dehydrations in the same active site with different substrates, which results from proton abstraction of stereochemically equivalent protons. These experiments illustrate how Nature could have utilized the (beta/alpha)8-barrel as a scaffold to evolve new activities.</dc:description>
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  Previous issue date: 2005</dc:description>
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Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
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          <dc:title>Natural and Engineered Promiscuity Within the Enolase Superfamily</dc:title>
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            <grantor>University of Illinois at Urbana-Champaign</grantor>
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