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| is due to a missing proton from the -COOH (</span>[https://teaching.ncl.ac.uk/bms/wiki/extensions/FCKeditor/fckeditor/editor/Carboxylic%20acid <span style="color:#0013A9">carboxylic acid</span>]<span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">) group. Aspartic acid has the | | is due to a missing proton from the -COOH (</span>[https://teaching.ncl.ac.uk/bms/wiki/extensions/FCKeditor/fckeditor/editor/Carboxylic%20acid <span style="color:#0013A9">carboxylic acid</span>]<span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">) group. Aspartic acid has the |
| chemical formula HOOCCH(NH</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">2</sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">)CH</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">2. </sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">Aspartic acid along | | chemical formula HOOCCH(NH</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">2</sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">)CH</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">2. </sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;">Aspartic acid along |
| with glutamic acid is the only acidic amino acid with a pk</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">a</sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;"> of 3.86.</span> | | with glutamic acid is the only acidic amino acid with a pk</span><sub style="font-family: Helvetica; line-height: 1.5em; text-align: justify;">a</sub><span style="font-family: Helvetica; font-size: 13pt; line-height: 1.5em; text-align: justify;"> of 3.86. T</span><span lang="EN-US" style="font-size:13.0pt;font-family:Helvetica;mso-bidi-font-family:Helvetica">he |
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| UnhideWhenUsed="false" QFormat="true" Name="Subtle Reference"/>
| |
| <w:LsdException Locked="false" Priority="32" SemiHidden="false"
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| UnhideWhenUsed="false" QFormat="true" Name="Intense Reference"/>
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| <w:LsdException Locked="false" Priority="33" SemiHidden="false"
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| UnhideWhenUsed="false" QFormat="true" Name="Book Title"/>
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| <w:LsdException Locked="false" Priority="37" Name="Bibliography"/>
| |
| <w:LsdException Locked="false" Priority="39" QFormat="true" Name="TOC Heading"/>
| |
| </w:LatentStyles>
| |
| </xml><![endif]--> <!--[if gte mso 10]>
| |
| <style>
| |
| /* Style Definitions */
| |
| table.MsoNormalTable
| |
| {mso-style-name:"Table Normal";
| |
| mso-tstyle-rowband-size:0;
| |
| mso-tstyle-colband-size:0;
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| mso-style-noshow:yes;
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| mso-style-priority:99;
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| mso-style-parent:"";
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| mso-padding-alt:0cm 5.4pt 0cm 5.4pt;
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| mso-para-margin:0cm;
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| mso-para-margin-bottom:.0001pt;
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| mso-pagination:widow-orphan;
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| font-size:12.0pt;
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| font-family:Cambria;
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| mso-ascii-font-family:Cambria;
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| mso-ascii-theme-font:minor-latin;
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| mso-hansi-font-family:Cambria;
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| mso-hansi-theme-font:minor-latin;
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| mso-ansi-language:EN-US;}
| |
| </style>
| |
| <![endif]--> <!--StartFragment--> <span lang="EN-US" style="font-size:13.0pt;font-family:Helvetica;mso-bidi-font-family:Helvetica">The
| |
| amino acid has both ‘L’ and ‘D’ isomers, and the </span><span lang="EN-US" style="font-size:11.0pt;font-family:Helvetica;mso-bidi-font-family:Helvetica">L</span><span lang="EN-US" style="font-size:13.0pt;font-family:Helvetica;mso-bidi-font-family: Helvetica">-isomer of aspartate is one of the 22 [http://en.wikipedia.org/wiki/Proteinogenic_amino_acid <span style="color:#0013A9">proteinogenic</span>] amino acids (those that are the building blocks of proteins). Most chemical syntheses will produce a ‘DL-aspartic acid’ which is a racemic mixture.</span> | | amino acid has both ‘L’ and ‘D’ isomers, and the </span><span lang="EN-US" style="font-size:11.0pt;font-family:Helvetica;mso-bidi-font-family:Helvetica">L</span><span lang="EN-US" style="font-size:13.0pt;font-family:Helvetica;mso-bidi-font-family: Helvetica">-isomer of aspartate is one of the 22 [http://en.wikipedia.org/wiki/Proteinogenic_amino_acid <span style="color:#0013A9">proteinogenic</span>] amino acids (those that are the building blocks of proteins). Most chemical syntheses will produce a ‘DL-aspartic acid’ which is a racemic mixture.</span> |
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