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148
CHAPTER 11. APPENDICES
<code>P</code>
<formula>C5H7N1O1</formula>
</mnm>
</monomers>
<modifs>
<mdf>
<name>OnAnyMonomer</name>
<formula>+Hec</formula>
<targets>*</targets>
</mdf>
<mdf>
<name>OnNoMonomer</name>
<formula>+Hec</formula>
<targets>!</targets>
</mdf>
<mdf>
<name>Phosphorylation</name>
<formula>-H+H2PO3</formula>
<targets>;S;T;Y;</targets>
</mdf>
<mdf>
<name>Sulphation</name>
<formula>-H+HSO3</formula>
<targets>;S;T;Y;</targets>
</mdf>
<mdf>
<name>Oxidation</name>
<formula>+O</formula>
<targets>;M;</targets>
</mdf>
<mdf>
<name>Acetylation</name>
<formula>-H+C2H3O</formula>
<targets>;K;</targets>
</mdf>
<mdf>
<name>AmidationGlu</name>
<formula>-OH+NH2</formula>
<targets>;E;</targets>
</mdf>
<mdf>
<name>AmidationAsp</name>
<formula>-OH+NH2</formula>
<targets>;D;</targets>
</mdf>
<mdf>
<name>SulfideBond</name>
<formula>-H2</formula>
<targets>;C;</targets>
</mdf>