Amino acids: structure and peptide bond formation

Cards (62)

  • What is the chemical formula for the carboxyl group in amino acids?
    -COOH
  • What is the position of the carboxyl group in the general structure of an amino acid?
    It is attached to the alpha carbon
  • What is the role of the alpha carbon in an amino acid?
    It is the central carbon atom
  • In the general structure of an amino acid, what is the position of the amino group relative to the alpha carbon?
    It is attached to the alpha carbon
  • How does the structure of an amino acid contribute to its function in proteins?
    The R group varies, affecting protein properties
  • What does the general structure of an amino acid include?
    Alpha carbon, amino group, carboxyl group, R group
  • What is the chemical formula for the amino group in amino acids?
    -NH₂
  • What is the general structure of an amino acid?
    • Central alpha carbon (α-C)
    • Amino group (-NH₂) attached
    • Carboxyl group (-COOH) attached
    • R group attached
  • What are the main components of an amino acid?
    • Alpha carbon (α-C): Central carbon atom
    • Amino group (-NH₂): Basic properties
    • Carboxyl group (-COOH): Acidic properties
    • R group: Variable group determining identity
  • What do the different R groups represent in the general structure of an amino acid?
    They represent the different amino acids
  • What does the R group in an amino acid determine?
    The identity of the amino acid
  • What are the key concepts related to peptide bonds?
    • Peptide Bond: Covalent bond linking amino acids
    • Formation: Occurs through dehydration reaction
    • Stability: Strong bond within protein backbone
  • What is a peptide bond?
    A covalent bond between amino acids
  • What is the purpose of the peptide bond formation process?
    To link amino acids together to form a polypeptide chain
  • What are amino acids known as in biology?
    Building blocks of proteins
  • What type of reaction occurs during peptide bond formation?
    A dehydration reaction
  • What are the steps in forming a peptide bond?
    1. -OH from carboxyl and H from amino combine to form H₂O
    2. A C-N bond forms between carbon and nitrogen
    3. Creates a peptide linkage joining two amino acids
  • What is the general structure of an amino acid?
    R-C-C-OH
  • What is the stability of a peptide bond?
    It is a strong bond within protein backbone
  • What is released during the formation of a peptide bond?
    Water (H₂O)
  • How do the different R groups in amino acids lead to their diversity?
    • The R groups can be:
    • Nonpolar (hydrophobic)
    • Polar (uncharged)
    • Positively charged (basic)
    • Negatively charged (acidic)
    • This diversity in R groups gives amino acids different chemical properties and functions.
  • If the R group of one of the amino acids in the peptide bond is a methyl group (-CH3), what would the formula for that amino acid be?
    CH3CHCOOHCH_3-CH-COOH
  • What are the main components of the general structure of an amino acid?
    • R group
    • Central carbon atom
    • Amino group (-NH2)
    • Carboxyl group (-COOH)
  • How do the N-terminus and C-terminus play a role in protein structure and function?
    • Determine the orientation and folding of the protein
    • Participate in interactions that stabilize the protein structure
    • Serve as sites for post-translational modifications that regulate protein activity
  • How does the arrangement of components around the alpha carbon affect amino acid structure?
    It determines the amino acid's properties
  • What are the three main types of R groups in amino acids?
    • Nonpolar: Hydrophobic, not charged or polar
    • Polar: Hydrophilic, slightly charged
    • Charged: Carry a positive or negative charge
  • What distinguishes different amino acids?
    The R group
  • What are the key steps in the peptide bond formation process?
    1. Amino group (NH2) of one amino acid reacts with the carboxyl group (COOH) of another amino acid
    2. A covalent peptide bond is formed, releasing a water molecule (H2O)
    3. The resulting polypeptide chain has a free amino group at one end and a free carboxyl group at the other end
  • What determines the specific properties of amino acids?
    R groups
  • What is the central carbon atom in an amino acid called?
    Alpha carbon
  • What is the chemical structure of the N-terminus and C-terminus in a protein?
    • N-terminus: Amino group (-NH2)
    • C-terminus: Carboxyl group (-COOH)
  • What is the chemical formula for the amino group (-NH2) at the N-terminus?

    H2N-
  • What is the chemical formula for the carboxyl group (-COOH) at the C-terminus?
    -COOH
  • How do variations in R groups affect amino acids?
    They affect interactions within protein structures
  • What is the name of the process shown in the image?
    Peptide bond formation
  • What does the resulting peptide bond (C=ONH) create?
    A stable connection in the protein backbone
  • If you wanted to determine the orientation of a protein, which terminus would you focus on?
    The N-terminus
  • What are the 5 amino acids with electrically charged side chains?
    • Arginine (Arg, R)
    • Histidine (His, H)
    • Lysine (Lys, K)
    • Aspartic Acid (Asp, D)
    • Glutamic Acid (Glu, E)
  • What is the role of the H and OH groups in the peptide bond formation?
    • The H and OH groups are released as a water molecule (H2O) during the formation of the peptide bond
    • This dehydration synthesis reaction links the amino and carboxyl groups of adjacent amino acids
  • How does the peptide bond formation process relate to the structure and function of proteins?
    • Peptide bonds link amino acids into polypeptide chains
    • The sequence and interactions of these polypeptide chains determine the 3D structure of proteins
    • The 3D structure of proteins is critical for their biological functions, such as catalysis, structural support, and signaling