Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
13th Edition
ISBN: 9780134421353
Author: Karen C. Timberlake
Publisher: PEARSON
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Textbook Question
Chapter 16.3, Problem 16.21PP
What type of interaction would you expect between the R groups of the following amino acids in a tertiary structure?
- Cysteine and cysteine
- Aspartate and lysine
- Serine and aspartate
- Leucine and leucine
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Draw the zwitterion of each of the following amino acids:
Glycine
Cysteine
Threonine
Alanine
Draw the zwitterion of each of the following amino acids:
Phenylalanine
Methionine
Leucine
Valine
Draw and name the structures of the proteins represented by the polypeptide chain below
a. serine-glutamic acid-arginine- isoleucine
b. beta-aspartic acid- alanine - asparagine
c. Cysteine-Proline-Threonine-asparagine- arginine-Isoleucine
Part C. Give the structure of the following and encircle the peptide bond
1. Glycyl - Seryl - Valine
2. Alanyl - Isoleucine
3. Prolyl - Leucine
4. Methionyl - Aspargyl - Glycine
5. Glutamyl - Methionyl - Isoleucine
Part D. Draw the structure
1. L valine
2. L leucine
3. L serine
4. D aspartic acid
5. D glycine
Chapter 16 Solutions
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Ch. 16.1 - Classify each of the following proteins according...Ch. 16.1 - Prob. 16.2PPCh. 16.1 - Prob. 16.3PPCh. 16.1 - Prob. 16.4PPCh. 16.1 - Draw the structure for each of the following amino...Ch. 16.1 - Draw the structure for each of the following amino...Ch. 16.1 - Draw the strcture for each of the following amino...Ch. 16.1 - Prob. 16.8PPCh. 16.1 - Prob. 16.9PPCh. 16.1 - Prob. 16.10PP
Ch. 16.2 - Prob. 16.11PPCh. 16.2 - Prob. 16.12PPCh. 16.2 - Prob. 16.13PPCh. 16.2 - Prob. 16.14PPCh. 16.2 - Prob. 16.15PPCh. 16.2 - Prob. 16.16PPCh. 16.3 - Prob. 16.17PPCh. 16.3 - Prob. 16.18PPCh. 16.3 - Prob. 16.19PPCh. 16.3 - Prob. 16.20PPCh. 16.3 - What type of interaction would you expect between...Ch. 16.3 - What type of interaction would you expect between...Ch. 16.3 - Prob. 16.23PPCh. 16.3 - Prob. 16.24PPCh. 16.3 - Prob. 16.25PPCh. 16.3 - Prob. 16.26PPCh. 16.3 - Prob. 16.27PPCh. 16.3 - Indicate the changes in secondary and tertiary...Ch. 16.4 - Why do chemical reactions in the body require...Ch. 16.4 - Prob. 16.30PPCh. 16.4 - Prob. 16.31PPCh. 16.4 - Prob. 16.32PPCh. 16.4 - Prob. 16.33PPCh. 16.4 - Prob. 16.34PPCh. 16.4 - Prob. 16.35PPCh. 16.4 - 16.36 Match the terms (1) active site, (2)...Ch. 16.4 - Prob. 16.37PPCh. 16.4 - Prob. 16.38PPCh. 16.4 - Prob. 16.39PPCh. 16.4 - Prob. 16.40PPCh. 16.4 - For problems 16.39 to 16.42, see Chemistry Link to...Ch. 16.4 - Prob. 16.42PPCh. 16.5 - Trypsin, a peptidase that hydrolyzes polypeptides,...Ch. 16.5 - pepsin, a peptidase that hydrolyzes proteins,...Ch. 16.5 - The following graph shows the activity versus pH...Ch. 16.5 - The following graph shows the activity versus pH...Ch. 16.5 - Prob. 16.47PPCh. 16.5 - Prob. 16.48PPCh. 16.5 - Prob. 16.49PPCh. 16.5 - Prob. 16.50PPCh. 16.5 - What is the chemical formula for hydroxyurea?Ch. 16.5 - What is the molar mass of hydroxyurea?Ch. 16.5 - Prob. 16.53PPCh. 16.5 - Prob. 16.54PPCh. 16 - Prob. 16.55UTCCh. 16 - Prob. 16.56UTCCh. 16 - Prob. 16.57UTCCh. 16 - Prob. 16.58UTCCh. 16 - 16.59 Identify the amino acids and type of...Ch. 16 - What type of interaction would you expect between...Ch. 16 - Draw the condensed structural formula for...Ch. 16 - Draw the condensed structural formula for...Ch. 16 - Seed and vegetables are often deficient in one or...Ch. 16 - 16.64 Seeds and vegetables are often deficient in...Ch. 16 - Prob. 16.65APPCh. 16 - Prob. 16.66APPCh. 16 - Prob. 16.67APPCh. 16 - Prob. 16.68APPCh. 16 - Prob. 16.69APPCh. 16 - Why do enzymes function only under mild...Ch. 16 - Prob. 16.71APPCh. 16 - Prob. 16.72APPCh. 16 - Prob. 16.73APPCh. 16 - Prob. 16.74APPCh. 16 - Prob. 16.75APPCh. 16 - Prob. 16.76APPCh. 16 - Prob. 16.77APPCh. 16 - Prob. 16.78APPCh. 16 - If a blood test indicates a high level of LDH and...Ch. 16 - Prob. 16.80APPCh. 16 - Prob. 16.81CPCh. 16 - Prob. 16.82CP
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- Draw the zwitterion structure for each of the following amino acids. a. Serine b. Methionine c. Threonine d. Phenylalaninearrow_forwardGive one example of a conjugated protein that contains the following prosthetic group: a.iron b.lipid c.phosphate group d.carbohydrate e.hemearrow_forwardShow the structures of the following amino acids in their zwitterionic forms: (a) Trp (b) Ile (c) Cys (d) Hisarrow_forward
- Identify the following amino acid in aqueous form (at pH = 7.0): (COO)–CH(NH3)–CH(OH)–CH3A. threonineB. glutamic acidC. histidineD. aspartic acidE. lysinearrow_forwardDraw Fischer projection formulas for the following amino acids. a. L-Serine b. D-Serine c. D-Alanine d. L-Leucinearrow_forwardDraw three-dimensional representations of the following amino acids. Explain their structures. (a) L-phenylalanine (b) L-histidine (c) D-serine (d) L-tryptophanarrow_forward
- Draw three-dimensional representations of the following amino acids. ) d-serinearrow_forwardDraw the positive ion (acidic ion) of each of the amino acids at a pH below 1.0 Glycine Cysteine Threonine Alaninearrow_forwardIdentify the R group of the side chain in the following amino acids that results in the side-chain classification indicated in parentheses a. cysteine (neutral, polar)b. arginine (basic, polar)c. valine (neutral, nonpolar)d. aspartate (acidic, polar)arrow_forward
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