
Organic And Biological Chemistry
7th Edition
ISBN: 9781305638686
Author: H. Stephen Stoker
Publisher: Brooks Cole
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 9, Problem 9.111EP
Interpretation Introduction
Interpretation:
The comparison of the non-covalent interactions responsible for tertiary proteins with those responsible for quaternary structure has to be stated.
Concept introduction:
The three-dimensional shape of the proteins obtained as a result of the interactions between the amino acid side chains is called the tertiary protein structure.
The highest level of organization of protein is the quaternary structure. Only the multimeric proteins have the quaternary structure.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Steps and explanation
Steps and explanations please.
Steps on how to solve. Thank you!
Chapter 9 Solutions
Organic And Biological Chemistry
Ch. 9.1 - Prob. 1QQCh. 9.1 - Proteins are naturally occurring unbranched...Ch. 9.2 - Prob. 1QQCh. 9.2 - How do the various standard amino acids differ...Ch. 9.2 - The number of carboxyl groups and amino groups...Ch. 9.2 - How many different subclassifications are there...Ch. 9.2 - Which of the following statements concerning...Ch. 9.3 - Prob. 1QQCh. 9.3 - Proteins from plant sources are a. always complete...Ch. 9.3 - Incomplete dietary proteins contain inadequate...
Ch. 9.4 - Which of the following statements concerning the...Ch. 9.4 - Prob. 2QQCh. 9.4 - Which of the following statements concerning...Ch. 9.5 - Which of the standard amino acids exist as...Ch. 9.5 - Which of the following is the zwitterion ion...Ch. 9.5 - Which of the following is the structural form for...Ch. 9.6 - Cysteine is unique among standard amino acids in...Ch. 9.6 - Prob. 2QQCh. 9.7 - The joining together of two amino acids to form a...Ch. 9.7 - Prob. 2QQCh. 9.7 - Which of the following statements concerning the...Ch. 9.7 - What functional group is present in the bond...Ch. 9.7 - How many isomeric tripeptides can be formed from...Ch. 9.8 - The two best-known peptide hormones present in the...Ch. 9.8 - Which of the following peptides is an important...Ch. 9.9 - The term protein is generally reserved for...Ch. 9.9 - The presence of which of the following is a...Ch. 9.9 - Which of the following is not a distinguishing...Ch. 9.10 - Prob. 1QQCh. 9.10 - Prob. 2QQCh. 9.10 - Two different proteins that contain the same...Ch. 9.11 - Prob. 1QQCh. 9.11 - Prob. 2QQCh. 9.11 - Which of the following statements concerning the ...Ch. 9.12 - Interactions between amino acid R groups are...Ch. 9.12 - Prob. 2QQCh. 9.12 - R group interactions between which of the...Ch. 9.13 - Prob. 1QQCh. 9.13 - Prob. 2QQCh. 9.14 - The complete hydrolysis of a protein produces a...Ch. 9.14 - Which of the following statements concerning...Ch. 9.15 - Which of the following levels of protein structure...Ch. 9.15 - Which of the following does not involve protein...Ch. 9.15 - Which of the following is not a denaturing agent...Ch. 9.16 - Which of the following statements concerning...Ch. 9.16 - Prob. 2QQCh. 9.16 - Prob. 3QQCh. 9.16 - In which of the following pairs of proteins are...Ch. 9.17 - Insulin and human growth hormone are examples of...Ch. 9.17 - Myoglobin and transferrin are examples of a....Ch. 9.17 - Prob. 3QQCh. 9.18 - Prob. 1QQCh. 9.18 - Which of the following statements concerning basic...Ch. 9.18 - Which of the following statements about antibodies...Ch. 9.19 - Prob. 1QQCh. 9.19 - Prob. 2QQCh. 9.19 - In which of the following pairs of plasma...Ch. 9 - Prob. 9.1EPCh. 9 - What element is always present in proteins that is...Ch. 9 - What percent of a cells overall mass is accounted...Ch. 9 - Prob. 9.4EPCh. 9 - What is signified when an amino acid is designated...Ch. 9 - Prob. 9.6EPCh. 9 - Prob. 9.7EPCh. 9 - Indicate whether or not each of the following...Ch. 9 - Prob. 9.9EPCh. 9 - How many carbon atoms are present in the R group...Ch. 9 - Prob. 9.11EPCh. 9 - Prob. 9.12EPCh. 9 - Prob. 9.13EPCh. 9 - Prob. 9.14EPCh. 9 - Prob. 9.15EPCh. 9 - Prob. 9.16EPCh. 9 - Prob. 9.17EPCh. 9 - Prob. 9.18EPCh. 9 - Prob. 9.19EPCh. 9 - Prob. 9.20EPCh. 9 - Prob. 9.21EPCh. 9 - Prob. 9.22EPCh. 9 - In what way is the structure of the amino acid...Ch. 9 - Which two of the standard amino acids are...Ch. 9 - Prob. 9.25EPCh. 9 - Prob. 9.26EPCh. 9 - Indicate whether or not each of the following...Ch. 9 - Prob. 9.28EPCh. 9 - Prob. 9.29EPCh. 9 - Prob. 9.30EPCh. 9 - Prob. 9.31EPCh. 9 - Prob. 9.32EPCh. 9 - Prob. 9.33EPCh. 9 - Prob. 9.34EPCh. 9 - To which family of mirror-image isomers do nearly...Ch. 9 - In what way is the structure of glycine different...Ch. 9 - Draw Fischer projection formulas for the following...Ch. 9 - Draw Fischer projection formulas for the following...Ch. 9 - Prob. 9.39EPCh. 9 - Prob. 9.40EPCh. 9 - At room temperature, amino acids are solids with...Ch. 9 - At room temperature, most amino acids are not very...Ch. 9 - Draw the zwitterion structure for each of the...Ch. 9 - Draw the zwitterion structure for each of the...Ch. 9 - Draw the structure of serine at each of the...Ch. 9 - Prob. 9.46EPCh. 9 - Prob. 9.47EPCh. 9 - Most amino acids have isoelectric points between...Ch. 9 - Glutamic acid exists in two low-pH forms instead...Ch. 9 - Arginine exists in two high-pH forms instead of...Ch. 9 - Prob. 9.51EPCh. 9 - In a high-pH aqueous solution, indicate whether...Ch. 9 - When two cysteine molecules dimerize, what happens...Ch. 9 - What chemical reaction involving the cysteine...Ch. 9 - What two functional groups are involved in the...Ch. 9 - Prob. 9.56EPCh. 9 - Prob. 9.57EPCh. 9 - Prob. 9.58EPCh. 9 - Prob. 9.59EPCh. 9 - What are the two alternating structure units...Ch. 9 - Draw a complete condensed structural...Ch. 9 - Draw a complete condensed structural...Ch. 9 - With the help of Table 20-1, identify the amino...Ch. 9 - Prob. 9.64EPCh. 9 - Prob. 9.65EPCh. 9 - With the help of Table 20-1, assign an IUPAC name...Ch. 9 - Prob. 9.67EPCh. 9 - Draw condensed structural formulas for the...Ch. 9 - Prob. 9.69EPCh. 9 - For the tripeptide SerArgIle which amino acid...Ch. 9 - Prob. 9.71EPCh. 9 - Consider the tripeptide leucylvalyltryptophan. a....Ch. 9 - Explain why the notations SerCys and CysSer...Ch. 9 - Explain why the notations AlaGlyValAla and...Ch. 9 - Prob. 9.75EPCh. 9 - There are a total of six different amino acid...Ch. 9 - Compare the structures of the protein hormones...Ch. 9 - Compare the protein hormones oxytocin and...Ch. 9 - Prob. 9.79EPCh. 9 - Compare the structures of the peptide...Ch. 9 - Prob. 9.81EPCh. 9 - Prob. 9.82EPCh. 9 - Prob. 9.83EPCh. 9 - Prob. 9.84EPCh. 9 - Indicate whether each of the following statements...Ch. 9 - Indicate whether each of the following statements...Ch. 9 - Prob. 9.87EPCh. 9 - Two proteins with the same amino acid composition...Ch. 9 - Prob. 9.89EPCh. 9 - Prob. 9.90EPCh. 9 - Prob. 9.91EPCh. 9 - Prob. 9.92EPCh. 9 - Prob. 9.93EPCh. 9 - Prob. 9.94EPCh. 9 - Prob. 9.95EPCh. 9 - Prob. 9.96EPCh. 9 - Prob. 9.97EPCh. 9 - Prob. 9.98EPCh. 9 - Prob. 9.99EPCh. 9 - Why is the phrase unstructured segment of a...Ch. 9 - State the four types of attractive forces that...Ch. 9 - Prob. 9.102EPCh. 9 - Prob. 9.103EPCh. 9 - Prob. 9.104EPCh. 9 - Prob. 9.105EPCh. 9 - Prob. 9.106EPCh. 9 - Indicate whether each of the following statements...Ch. 9 - Prob. 9.108EPCh. 9 - Prob. 9.109EPCh. 9 - Prob. 9.110EPCh. 9 - Prob. 9.111EPCh. 9 - Quaternary protein structure is more easily...Ch. 9 - Prob. 9.113EPCh. 9 - Prob. 9.114EPCh. 9 - Prob. 9.115EPCh. 9 - Prob. 9.116EPCh. 9 - Prob. 9.117EPCh. 9 - How many different di- and tripeptides could be...Ch. 9 - Identify the primary structure of a hexapeptide...Ch. 9 - Identify the primary structure of a hexapeptide...Ch. 9 - Draw structural formulas for the products obtained...Ch. 9 - Prob. 9.122EPCh. 9 - Prob. 9.123EPCh. 9 - Why is complete hydrolysis of a protein not also...Ch. 9 - In what way is the protein in a cooked egg the...Ch. 9 - Why is cooked protein more easily digested than...Ch. 9 - Prob. 9.127EPCh. 9 - Indicate whether or not each of the following...Ch. 9 - Prob. 9.129EPCh. 9 - Prob. 9.130EPCh. 9 - Prob. 9.131EPCh. 9 - What is the major biochemical function of each of...Ch. 9 - Using the list in Section 20-17, characterize each...Ch. 9 - Prob. 9.134EPCh. 9 - Prob. 9.135EPCh. 9 - Prob. 9.136EPCh. 9 - What two nonstandard amino acids are present in...Ch. 9 - Prob. 9.138EPCh. 9 - Prob. 9.139EPCh. 9 - Prob. 9.140EPCh. 9 - Prob. 9.141EPCh. 9 - Prob. 9.142EPCh. 9 - Prob. 9.143EPCh. 9 - Describe the process by which blood...Ch. 9 - Prob. 9.145EPCh. 9 - Prob. 9.146EPCh. 9 - Prob. 9.147EPCh. 9 - Prob. 9.148EPCh. 9 - Prob. 9.149EPCh. 9 - As the lipid content of a plasma lipoprotein...Ch. 9 - Prob. 9.151EPCh. 9 - Prob. 9.152EP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- 3. Name this ether correctly. H₁C H3C CH3 CH3 4. Show the best way to make the ether in #3 by a Williamson Ether Synthesis. Start from an alcohol or phenol. 5. Draw the structure of an example of a sulfide.arrow_forward1. Which one(s) of these can be oxidized with CrO3 ? (could be more than one) a) triphenylmethanol b) 2-pentanol c) Ethyl alcohol d) CH3 2. Write in all the product(s) of this reaction. Label them as "major" or "minor". 2-methyl-2-hexanol H2SO4, heatarrow_forward3) Determine if the pairs are constitutional isomers, enantiomers, diastereomers, or mesocompounds. (4 points)arrow_forward
- In the decomposition reaction in solution B → C, only species C absorbs UV radiation, but neither B nor the solvent absorbs. If we call At the absorbance measured at any time, A0 the absorbance at the beginning of the reaction, and A∞ the absorbance at the end of the reaction, which of the expressions is valid? We assume that Beer's law is fulfilled.arrow_forward> You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: 1. ☑ CI 2. H3O+ O Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. Explanation Check ? DO 18 Ar B © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardDon't use ai to answer I will report you answerarrow_forward
- Consider a solution of 0.00304 moles of 4-nitrobenzoic acid (pKa = 3.442) dissolved in 25 mL water and titrated with 0.0991 M NaOH. Calculate the pH at the equivalence pointarrow_forwardWhat is the name of the following compound? SiMe3arrow_forwardK Draw the starting structure that would lead to the major product shown under the provided conditions. Drawing 1. NaNH2 2. PhCH2Br 4 57°F Sunny Q Searcharrow_forward
- 7 Draw the starting alkyl bromide that would produce this alkyne under these conditions. F Drawing 1. NaNH2, A 2. H3O+ £ 4 Temps to rise Tomorrow Q Search H2arrow_forward7 Comment on the general features of the predicted (extremely simplified) ¹H- NMR spectrum of lycopene that is provided below. 00 6 57 PPM 3 2 1 0arrow_forwardIndicate the compound formula: dimethyl iodide (propyl) sulfonium.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- World of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College DivChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning

General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning

Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,

World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning

World of Chemistry
Chemistry
ISBN:9780618562763
Author:Steven S. Zumdahl
Publisher:Houghton Mifflin College Div

Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning

Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Biomolecules - Protein - Amino acids; Author: Tutorials Point (India) Ltd.;https://www.youtube.com/watch?v=ySNVPDHJ0ek;License: Standard YouTube License, CC-BY