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Fundamentals of Biochemistry
Fourth Edition Donald Voet • Judith G. Voet • Charlotte W. Pratt Chapter 4 Amino Acids Copyright © 2013 by John Wiley & Sons, Inc. All rights reserved.
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Chapter 4 Amino Acid Structure Key Concepts 4.1
• The 20 standard amino acids share a common structure but differ in their side chains. • Peptide bonds link amino acid residues in a polypeptide. • Some amino acid side chains contain ionizable groups whose pK values may vary.
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General Structure of α-Amino Acid
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Structures of Standard Amino Acids
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Structures of Standard Amino Acids
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Structures of Standard Amino Acids
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Structures of Standard Amino Acids
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Dipolar Amino Acid: Zwitterion
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Condensation of Two Amino Acids
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Nonpolar Side Chains
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Uncharged Polar Side Chains
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Cysteine Can Form Disulfide Bonds
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Charged Polar Side Chains
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Alanyltyrosylaspartylglycine
Ala-Tyr-Asp-Gly AYDG
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Amino Acid Nomenclature
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Chapter 4 Amino Acid Structure Checkpoint 4.1
• Draw a generic amino acid and identify the carbon and its substituents. • Draw the structures of the 20 standard amino acids and give their one- and three-letter abbreviations. • Draw a Cys–Gly–Asn tripeptide. Identify the peptide bond and the N- and C-termini, and determine the peptide’s net charge at neutral pH. • Classify the 20 standard amino acids by polarity, structure, type of functional group, and acid–base properties. • Why do the pK values of ionizable groups differ between free amino acids and amino acid residues in polypeptides?
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Chapter 4 Stereochemistry Key Concepts 4.2
• Amino acids and many other biological compounds are chiral molecules whose configurations can be depicted by Fischer projections. • The amino acids in proteins all have the L stereochemical configuration.
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Modified Amino Acids in Proteins
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Biologically Active Amino Acid Derivatives
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Dimerization of Glutathione
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