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chapter5.aux
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\@writefile{toc}{\contentsline {section}{ Author Contributions}{85}}
\@writefile{toc}{\contentsline {section}{ Abstract}{85}}
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\@writefile{toc}{\contentsline {section}{ Introduction}{86}}
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\@writefile{toc}{\contentsline {section}{ Results}{88}}
\@writefile{toc}{\contentsline {subsection}{ Human S100A5 and S100A6 interact with diverse peptides at the same binding site}{88}}
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\@writefile{toc}{\contentsline {subsection}{ The S100A5 and S100A6 clades exhibit conserved binding specificity}{91}}
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\@writefile{toc}{\contentsline {subsection}{ Specificity evolved from an apparently promiscuous ancestor}{96}}
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\@writefile{toc}{\contentsline {subsection}{ Binding specificity can be changed with a single mutation}{97}}
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\@writefile{lof}{\contentsline {figure}{\numberline {18}{\ignorespaces Small changes are sufficient to alter binding specificity}}{99}}
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\@writefile{toc}{\contentsline {subsection}{ Low specificity through a hydrophobic interface}{101}}
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\@writefile{toc}{\contentsline {subsection}{ S100s may allow the evolution of new calcium regulation}{102}}
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\@writefile{toc}{\contentsline {section}{ Materials and Methods}{105}}
\@writefile{toc}{\contentsline {subsection}{ Molecular cloning, expression and purification of proteins}{105}}
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\@writefile{toc}{\contentsline {subsection}{ Isothermal titration calorimetry}{107}}
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\@writefile{toc}{\contentsline {subsection}{ 2D HSQC NMR experiments}{108}}
\@writefile{toc}{\contentsline {subsection}{ Far--UV CD spectroscopy}{108}}
\@writefile{toc}{\contentsline {subsection}{ Preparation of biotinylated proteins for phage display}{109}}
\@writefile{toc}{\contentsline {subsection}{ Phage display panning }{110}}
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\@writefile{toc}{\contentsline {section}{ Bridge to Chapter VI}{114}}
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