Calculate the fractional ionization of each functional group of the amino acid: Cysteine of the following...
What are functional groups in this molecule? H HN-C-COOH CH, sulfhydryl group ✓ carboxyl group ✓amino group methyl group
Fill in the blanks for each amino acid
Amino Acid Properties Name of R-group Properties Amino Acid Type of Polarity pKa Charge at Special functional group pH-7 Properties (hn(wpp)amgies applicable) (whpee Alanine Arginine Asparagine Aspartate Carboxyl Polar 3.9 Sulfhydryl Polar N/A Forms S-S Glutamine Glutamate Histidine Isoleucine Lysine Methionine Phenylalanine Aromatic Non-Polar Absorbs G@ 280 nm N/A Proline Can be Serine Threonine Tryptophane Tyrosine Valine
Titrate an amino acid that isn’t acidic or basic and also doesn’t have a titratable group on its R that will be ionized starting from ph 1-14 with the ionization of the side groups. When will they lose their protons, what are the weak acid of the carboxyl and discuss the titration of the carboxyl and amino groups. Illistrate the two charged groups on the amino acid at neutral, acidic and basic pH. whats the pH of charged groups when...
a-carboxyl group pka Amino acid Ala a-amino group pka 9.7 2.3 Arg 9.0 9.0 Asnor Gin Asp or Glu Cys 9.8 10.8 His 9.2 9.2 9.1 Calculate the pl of ASN: 6.0 2.5 5.5 10.7 5.0
5. Amino acid titration. The graph below shows a titration of an amino acid with NaOH. This experiment reveals several important features of this amino acid. A) What is the identity of the amino acid? [Write its full name.] B) Match the following points in the titration curve. [In the space beside each description (left), write a number (1-6) corresponding to a specific pH (right).] The amino acid is fully protonated. 1) pH=0.0 PH The amino acid is fully deprotonated....
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) он penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) СH3NH2 снзон HBr СHЗCH2CH2CH2СH3 HF
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HBr CH3CH2CH2CH2CH3
Answer the following questions. For calculations, show all work. You may attach another sheet of paper (2 pt) 1. List all of the amino acids that have side chains that fit into each of the following categories: a. acidic: b. basic: c. nonpolar aromatic: d. sulfur-containing: e. hydroxyl-containing: f. achiral: (2 pt) 2. Protein Lengths. Calculate the length of a 80 amino acid-long stretch of protein if: a. It consists of pure a-helices: b. It consists of pure β strands:-...
23. How many titratable functional groups do each of the following amino acids possess? a. isoleucine ______________ b. glutamic acid ______________ c. tyrosine ______________ d. lysine ______________
Draw the following peptide tyrosine-cysteine-lysine-leucine. Identify the functional groups of the side chains by name and label the peptide bonds, the N-terminus, and the C-terminus of the peptide. Also, what is the one letter code? Draw the membrane lipid phosphatidylserine with stearic acid and oleic acid attached to the glycerol-3-phosphate backbone in position 1 and 2, respectively. How are the individual parts of the molecule (glycerol, phosphate, serine, and fatty acids) connected to each other?