Third Exam Practice Test

Similar documents
AA s are the building blocks of proteins

INTRODUCTION TO BIOCHEMISTRY/POLYMERS. 3. With respect to amino acids, polypeptides, and proteins, know:

1. Describe the relationship of dietary protein and the health of major body systems.

BIOCHEMISTRY REVIEW. Overview of Biomolecules. Chapter 4 Protein Sequence

Amino Acids. Amino Acids. Fundamentals. While their name implies that amino acids are compounds that contain an NH. 3 and CO NH 3

1-To know what is protein 2-To identify Types of protein 3- To Know amino acids 4- To be differentiate between essential and nonessential amino acids

LAB#23: Biochemical Evidence of Evolution Name: Period Date :

Chemistry 121 Winter 17

Objective: You will be able to explain how the subcomponents of

1. (38 pts.) 2. (25 pts.) 3. (15 pts.) 4. (12 pts.) 5. (10 pts.) Bonus (12 pts.) TOTAL (100 points)

9/6/2011. Amino Acids. C α. Nonpolar, aliphatic R groups

Molecular Biology. general transfer: occurs normally in cells. special transfer: occurs only in the laboratory in specific conditions.

Organic Chemistry 3540

Gentilucci, Amino Acids, Peptides, and Proteins. Peptides and proteins are polymers of amino acids linked together by amide bonds CH 3

Biological systems interact, and these systems and their interactions possess complex properties. STOP at enduring understanding 4A

Biomolecules: amino acids

Moorpark College Chemistry 11 Fall Instructor: Professor Gopal. Examination # 5: Section Five May 7, Name: (print)

Properties of amino acids in proteins

CHAPTER 21: Amino Acids, Proteins, & Enzymes. General, Organic, & Biological Chemistry Janice Gorzynski Smith

For questions 1-4, match the carbohydrate with its size/functional group name:

2. Which of the following amino acids is most likely to be found on the outer surface of a properly folded protein?

(30 pts.) 16. (24 pts.) 17. (20 pts.) 18. (16 pts.) 19. (5 pts.) 20. (5 pts.) TOTAL (100 points)

Midterm 1 Last, First

Reactions and amino acids structure & properties

Practice Problems 3. a. What is the name of the bond formed between two amino acids? Are these bonds free to rotate?

CS612 - Algorithms in Bioinformatics

Amino acids-incorporated nanoflowers with an

For questions 1-4, match the carbohydrate with its size/functional group name:

Chemical Nature of the Amino Acids. Table of a-amino Acids Found in Proteins

endopeptidases aminopeptidases carboxypeptidases hydrolyzes a peptide bond somewhere in the middle of the polypeptide

PROTEINS. Amino acids are the building blocks of proteins. Acid L-form * * Lecture 6 Macromolecules #2 O = N -C -C-O.

Cells N5 Homework book

Page 8/6: The cell. Where to start: Proteins (control a cell) (start/end products)

The Structure and Function of Large Biological Molecules Part 4: Proteins Chapter 5

Towards a New Paradigm in Scientific Notation Patterns of Periodicity among Proteinogenic Amino Acids [Abridged Version]

(65 pts.) 27. (10 pts.) 28. (15 pts.) 29. (10 pts.) TOTAL (100 points) Moorpark College Chemistry 11 Spring Instructor: Professor Gopal

Short polymer. Dehydration removes a water molecule, forming a new bond. Longer polymer (a) Dehydration reaction in the synthesis of a polymer

AP Bio. Protiens Chapter 5 1

Lecture 4. Grouping Amino Acid 7/1/10. Proteins. Amino Acids. Where Are Proteins Located. Nonpolar Amino Acids

A Chemical Look at Proteins: Workhorses of the Cell

Methionine (Met or M)

Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Classification of amino acids: -

Chapter 21 Lecture Outline

Biology. Lectures winter term st year of Pharmacy study

If you like us, please share us on social media. The latest UCD Hyperlibrary newsletter is now complete, check it out.

Chapter 20 and GHW#10 Questions. Proteins

Proteins are sometimes only produced in one cell type or cell compartment (brain has 15,000 expressed proteins, gut has 2,000).

Organic Chemistry 3540

This exam consists of two parts. Part I is multiple choice. Each of these 25 questions is worth 2 points.

Introduction to Peptide Sequencing

Four Classes of Biological Macromolecules. Biological Macromolecules. Lipids

Moorpark College Chemistry 11 Fall Instructor: Professor Gopal. Examination #5: Section Five December 7, Name: (print) Section:

Lipids: diverse group of hydrophobic molecules

Biomolecules Amino Acids & Protein Chemistry

Macromolecules of Life -3 Amino Acids & Proteins

Chapter 3: Amino Acids and Peptides

paper and beads don t fall off. Then, place the beads in the following order on the pipe cleaner:

Amino acid metabolism

number Done by Corrected by Doctor Dr.Diala

The Structure and Function of Macromolecules

Amino Acids. Review I: Protein Structure. Amino Acids: Structures. Amino Acids (contd.) Rajan Munshi

Fundamentals of Organic Chemistry CHEM 109 For Students of Health Colleges

Metabolism of amino acids. Vladimíra Kvasnicová

Organic ChemI 3444Q, Columbia U, Su92, Exam 4 - Final Exam, 08/13/92; Dr. I.J. Borowitz 1

Protein Investigator. Protein Investigator - 3

Macromolecules Structure and Function

Four melanocyte-stimulating hormones have the following amino acid sequences:

Bio 366: Biological Chemistry II Test #1, 100 points (7 pages)

SIMPLE BASIC METABOLISM

Biological evaluation of analogues of an insect neuropeptide proctolin

AMINO ACID METABOLISM. Sri Widia A Jusman Dept. of Biochemistry & Molecular Biology FMUI

EFFECTS OF AMINO ACID SUBSTITUTIONS FOR WHEY PROTEIN CONCENTRATE ON WEANLING PIG PERFORMANCE. Authors: J. Chung, S.D. Carter and J.C.

Enzyme Catalytic Mechanisms. Dr. Kevin Ahern

7.012 F 04 Problem Set 1 September 10 th 2004

Amino Acids, Pep.des, and Proteins

9/16/15. Properties of Water. Benefits of Water. More properties of water

CHAPTER 29 HW: AMINO ACIDS + PROTEINS

Amino Acids. Lecture 4: Margaret A. Daugherty. Fall Swiss-prot database: How many proteins? From where?

AMINO ACIDS STRUCTURE, CLASSIFICATION, PROPERTIES. PRIMARY STRUCTURE OF PROTEINS

Cells. Variation and Function of Cells

Protein and Amino Acid Analysis. Chemistry M3LC

Charges on amino acids and proteins. ph 1. ph 7. Acidic side chains: glutamate and aspartate

Chemical Mechanism of Enzymes

PROTEINS. Building blocks, structure and function. Aim: You will have a clear picture of protein construction and their general properties

Study of Amino Acids in DDGS

Catabolism of Carbon skeletons of Amino acids. Amino acid metabolism

Biochemistry 2 Recita0on Amino Acid Metabolism

BIO th September, 1997

Previous Class. Today. Detection of enzymatic intermediates: Protein tyrosine phosphatase mechanism. Protein Kinase Catalytic Properties

استاذ الكيمياءالحيوية

BCHS 3304/ Exam I. September 26,

LC-MS Analysis of Amino Acids on a Novel Mixed-Mode HPLC Column

The Basics: A general review of molecular biology:

GL Science Inertsearch for LC Inertsil Applications - Acids. Data No. Column Data Title Solutes Eluent Detection Data No.

2. Ionization Sources 3. Mass Analyzers 4. Tandem Mass Spectrometry

MS/MS Scan Modes. Eötvös University, Budapest April 16, MS/MS Scan Modes. Árpád Somogyi. Product Ion Scan Select. Scan. Precursor Ion Scan Scan

BCMB Chapter 3 (part1)

1. (CH 3 ) 3 COCNHCHCOO 2. H, H 2 O

Transcription:

Third Exam Practice Test 1. A mixture of aspartic acid, methionine and arginine can be separated by electrophoresis. Explain how this would be done and what exactly happens during the separation. What would be the ideal p for conducting the separation? The isoelectric points for Asp, Met, and Arg are 2.77, 5.74, and 10.76 respectively. 2. The synthesis of alkylamines by direct substitution simple alkyl halides and ammonia is usually complicated by overalkylation. owever, this method is much more useful for the preparation of alpha-amino acids the corresponding alpha-halo acids. Why isn t overalkylation a significant problem in the preparation of alpha-amino acids? 3. Use the simple nucleophilic substitution method involving ammonia and the other appropriate alpha-halo acids to propose reaction sequences suitable for the preparation of each of the following amino acids the indicated starting materials and any other necessary reagents. 3 C C - 1-propanol C C - cyclopentene C - ethylene oxide (epoxide) and propane S C -

4. Use the Gabriel malonic ester methodology and propose reaction sequences suitable for the preparation of each of the following amino acids the indicated starting materials and any other necessary reagents. C - C - C - TP TP is an alcohol protecting group that can be removed with acid. C - 5. Give the expected major product each of the following reactions or reaction sequences: 1. 3, p 5 1. Cl/ 2 2. ac 2. -/ 2 CEt CEt Ph Cl/ 2 heat SC 3 C 2 Et C 2 Et 1. 2 2 2. -/ 2 3. 3, heat 6. When an unknown polypeptide was treated with 3M Cl, the following amino acids were produced: Tyr, Asp, Val, Glu (1 mmol each), and Ala (2 mmol). Treatment with 1M Cl resulted in partial hydrolysis. The following fragments were isolated: Glu-Tyr-Ala, Ala-Ala, and Asp-Glu-Tyr. Suggest a structure for the peptide consistent with the data provided.

7. Draw the PT derivative that was isolated after the second Edman degradation cycle involving the heptapeptide Tyr-Ile-glu-Asn-Cys-Pro-Ile. 8. Provide a sequence of reactions and the appropriate reagents suitable for the solid phase synthesis of the following tripeptide: Ala-Ile-Val. 9. Suggest suitable starting materials needed to prepare each of the following amino acids by reductive amination: a) threonine b) tryptophan c) lysine 10. The structure of an unknown nonapeptide (B) was determined by a combination of methods. n the basis of the data provided, suggest a structure for this peptide. Recall that chymotrypsin cleaves peptide bonds at the C terminal end of Phe, Tyr, and Trp. chymotrypsin B Ser-Pro-Phe Arg-Pro-Pro-Gly-Phe Arg B Edman Degradation Ph S 2 11. Draw the expected products of each of the following reactions or reaction sequences: Ph - 1. Cbz-Cl 2. glycine methyl ester DCC Thr-Ser-Lys 1. PhCS/ - 2. Cl/ 2 Ser-Lys 1. PhCS/ - 2. Cl/ 2 12. Give possible Strecker syntheses for the following amino acids: a) methionine b) lysine c) tyrosine d) valine

13. Suggest structures for compounds A and B and provide the missing reagents for the following reaction sequence: C 2 Et 1. Et- 1. A 3 2. C 2 Et 2. Zn/ Ac 2 B i 2 C C 2 Et C 2 Et Ac ii 2 C 2 C 2 14. Draw the product(s) that is (are) formed D-xylose in the Kiliani Fisher synthesis. C ac 2 2, 2 Pd/BaS 4 C 2 D-xylose 15. A D-hexose, annose (1) forms the same osazone as arpitose (2). Both give positive Tollens tests but negative bisulfite tests. ab 4 converts annose to danitol (3) and arpitose to julitol (4). Both products are optically active. Sugars 1 and 2 can be formed a D-Pentose, katherinose (5), which is converted to kristenitol (6) by ab 4. This product is optically inactive. Julitol can be obtained as well by the ab 4 reaction with L-melose (7). Identify 1 7 and give your reasoning. 16. A D-pentose, colleenose, is treated with a bacterium that causes epimerization at C-3 to give monose. Both pentoses afford optically inactive dicarboxylic acids with nitric acid. Colleenose was formed by a Fisher-Kiliani synthesis carolynose, a tetrose which give an optically active compound with ab 4. Identify the three sugars. Show your reasoning. 17. While Americans in Atlanta were gladly making gum in gallon tanks, Alsatians in Aachen were gladly mixing grain in Germanic tons. ne Alsatian names Fisher synthesized a D-hexose a D-pentose, whose product with nitric acid was optically inactive. The nitric acid treatment of the D-hexose did give an optically active product, which could not be made by the nitric acid reaction with any L- hexose. Identify the D-hexose and show your reasoning. 18. This Fisher proof was my final exam last year. ote the name of the D- hexose that Professor Mcelis chose.

Determine the structure of D-hexose, Pamelose. Pamelose and its epimer kamarose are both formed by Kiliani-Fisher D-pentose, clyrose. Treatment of D-hexose with ab 4 yields an optically active product. Treatment of D- pentose with ab 4 yields an optically inactive product. There is L-hexose that afforded Pamelose product but the product kamarose has no other source. 19. Give a mechanism for the Edman degradation of Ala-Ala using phenylthilocyanate. 20. Give the mechanism for the coupling of Gly-Ala using DCC. 21. Dilbert Dunker and Gangrene McCloskey have transferred to Louisiana Subnormal to become bayou chemists. They wished to synthesize a polypeptide by the Merrifield method. After activating the polystyrene beads with benzyl chloride groups they added amino acid A, followed by deprotection and then amino acid B to form the first peptide bond with DCC. They repeated the process 9 times. When the treated the resin with strong acid to free the peptide, no product was obtained. What was the problem? 22. Propose syntheses for the following: 3 3 -C C - - *For more questions on amines, please see the Amines review sheet posted at http://homepages.nyu.edu/~pmt213.