The Structure and Functions of Proteins

Similar documents
Proteins. Division Ave. High School Ms. Foglia AP Biology. Proteins. Proteins. Multipurpose molecules

Model Mélange. Physical Models of Peptides and Proteins

Conformational Geometry of Peptides and Proteins:

AP Biology. Proteins. AP Biology. Proteins. Multipurpose molecules

From Amino Acids to Proteins - in 4 Easy Steps

Properties of amino acids in proteins

titin, has 35,213 amino acid residues (the human version of titin is smaller, with only 34,350 residues in the full length protein).

A Gentle Introduction to (or Review of ) Fundamentals of Chemistry and Organic Chemistry

Protein Structure. W. M. Grogan, Ph.D. OBJECTIVES

Problem Set 1

Biomolecules: lecture 10

Objective: Students will be able identify peptide bonds in proteins and describe the overall reaction between amino acids that create peptide bonds.

Protein Structure Basics

Biomolecules: lecture 9

Physiochemical Properties of Residues

Secondary Structure. Bioch/BIMS 503 Lecture 2. Structure and Function of Proteins. Further Reading. Φ, Ψ angles alone determine protein structure

Protein Structure. Role of (bio)informatics in drug discovery. Bioinformatics

Overview. The peptide bond. Page 1

Ch 3: Chemistry of Life. Chemistry Water Macromolecules Enzymes

CHAPTER 29 HW: AMINO ACIDS + PROTEINS

LS1a Fall 2014 Problem Set #2 Due Monday 10/6 at 6 pm in the drop boxes on the Science Center 2 nd Floor

Molecular Modelling. part of Bioinformatik von RNA- und Proteinstrukturen. Sonja Prohaska. Leipzig, SS Computational EvoDevo University Leipzig

Major Types of Association of Proteins with Cell Membranes. From Alberts et al

Read more about Pauling and more scientists at: Profiles in Science, The National Library of Medicine, profiles.nlm.nih.gov

Announcements. Primary (1 ) Structure. Lecture 7 & 8: PROTEIN ARCHITECTURE IV: Tertiary and Quaternary Structure

Dana Alsulaibi. Jaleel G.Sweis. Mamoon Ahram

Peptides And Proteins

Advanced Certificate in Principles in Protein Structure. You will be given a start time with your exam instructions

Biochemistry Prof. S. DasGupta Department of Chemistry Indian Institute of Technology Kharagpur. Lecture - 06 Protein Structure IV

Dental Biochemistry EXAM I

Protein Structure. Hierarchy of Protein Structure. Tertiary structure. independently stable structural unit. includes disulfide bonds

Protein structure (and biomolecular structure more generally) CS/CME/BioE/Biophys/BMI 279 Sept. 28 and Oct. 3, 2017 Ron Dror

Biological Macromolecules

Section Week 3. Junaid Malek, M.D.

Introduction to Comparative Protein Modeling. Chapter 4 Part I

Lecture 26: Polymers: DNA Packing and Protein folding 26.1 Problem Set 4 due today. Reading for Lectures 22 24: PKT Chapter 8 [ ].

BIOCHEMISTRY Unit 2 Part 4 ACTIVITY #6 (Chapter 5) PROTEINS

Student Questions and Answers October 8, 2002

BIRKBECK COLLEGE (University of London)

1. Amino Acids and Peptides Structures and Properties

4 Proteins: Structure, Function, Folding W. H. Freeman and Company

Structure and evolution of the spliceosomal peptidyl-prolyl cistrans isomerase Cwc27

B O C 4 H 2 O O. NOTE: The reaction proceeds with a carbonium ion stabilized on the C 1 of sugar A.

AP Biology Unit 1, Chapters 2, 3, 4, 5

Bi 8 Midterm Review. TAs: Sarah Cohen, Doo Young Lee, Erin Isaza, and Courtney Chen

THE UNIVERSITY OF MANITOBA. PAPER NO: _1_ LOCATION: 173 Robert Schultz Theatre PAGE NO: 1 of 5 DEPARTMENT & COURSE NO: CHEM / MBIO 2770 TIME: 1 HOUR

MULTIPLE CHOICE. Circle the one alternative that best completes the statement or answers the question.

Packing of Secondary Structures

Basic Principles of Protein Structures

Protein Structure & Motifs

A) at equilibrium B) endergonic C) endothermic D) exergonic E) exothermic.

Protein Structure Bioinformatics Introduction

Protein Struktur (optional, flexible)

D Dobbs ISU - BCB 444/544X 1

1/23/2012. Atoms. Atoms Atoms - Electron Shells. Chapter 2 Outline. Planetary Models of Elements Chemical Bonds

Biochemistry - I SPRING Mondays and Wednesdays 9:30-10:45 AM (MR-1307) Lectures 3-4. Based on Profs. Kevin Gardner & Reza Khayat

Outline. Levels of Protein Structure. Primary (1 ) Structure. Lecture 6:Protein Architecture II: Secondary Structure or From peptides to proteins

Biochemistry Quiz Review 1I. 1. Of the 20 standard amino acids, only is not optically active. The reason is that its side chain.

Unit 1: Chemistry - Guided Notes

Chemistry Chapter 22

The Structure of Enzymes!

The Structure of Enzymes!

Supersecondary Structures (structural motifs)

Protein Structure and Function. Protein Architecture:

Biochemistry,530:,, Introduc5on,to,Structural,Biology, Autumn,Quarter,2015,

Outline. Levels of Protein Structure. Primary (1 ) Structure. Lecture 6:Protein Architecture II: Secondary Structure or From peptides to proteins

Chapter 2. Chemical Principles

BSc and MSc Degree Examinations

Introduction to Protein Folding

Exam I Answer Key: Summer 2006, Semester C

BCH 4053 Spring 2003 Chapter 6 Lecture Notes

4) Chapter 1 includes heredity (i.e. DNA and genes) as well as evolution. Discuss the connection between heredity and evolution?

Secondary and sidechain structures

Bonds and Structural Supports

Tamer Barakat. Razi Kittaneh. Mohammed Bio. Diala Abu-Hassan

Biomolecules. Energetics in biology. Biomolecules inside the cell

1. (5) Draw a diagram of an isomeric molecule to demonstrate a structural, geometric, and an enantiomer organization.

HOMOLOGY MODELING. The sequence alignment and template structure are then used to produce a structural model of the target.

CHMI 2227 EL. Biochemistry I. Test January Prof : Eric R. Gauthier, Ph.D.

Introduction to" Protein Structure

Denaturation and renaturation of proteins

Useful background reading

Biology 30 The Chemistry of Living Things

Chemical Properties of Amino Acids

Protein Structure Marianne Øksnes Dalheim, PhD candidate Biopolymers, TBT4135, Autumn 2013

MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

Enzyme Catalysis & Biotechnology

Ranjit P. Bahadur Assistant Professor Department of Biotechnology Indian Institute of Technology Kharagpur, India. 1 st November, 2013

Solutions In each case, the chirality center has the R configuration

1. What is an ångstrom unit, and why is it used to describe molecular structures?

PROTEIN STRUCTURE AMINO ACIDS H R. Zwitterion (dipolar ion) CO 2 H. PEPTIDES Formal reactions showing formation of peptide bond by dehydration:

Dihedral Angles. Homayoun Valafar. Department of Computer Science and Engineering, USC 02/03/10 CSCE 769

Part 7 Bonds and Structural Supports

Chapter 1 1) Biological Molecules a) Only a small subset of the known elements are found in living systems i) Most abundant- C, N, O, and H ii) Less

W2. Chemical structures of protein and DNA

Examples of Protein Modeling. Protein Modeling. Primary Structure. Protein Structure Description. Protein Sequence Sources. Importing Sequences to MOE

Chemical Principles. PowerPoint Lecture Presentations prepared by Bradley W. Christian, McLennan Community College C H A P T E R

Chem. 27 Section 1 Conformational Analysis Week of Feb. 6, TF: Walter E. Kowtoniuk Mallinckrodt 303 Liu Laboratory

Full file at

Prof. Jason Kahn Your Signature: Exams written in pencil or erasable ink will not be re-graded under any circumstances.

Transcription:

Wright State University CORE Scholar Computer Science and Engineering Faculty Publications Computer Science and Engineering 2003 The Structure and Functions of Proteins Dan E. Krane Wright State University - Main Campus, dan.krane@wright.edu Michael L. Raymer Wright State University - Main Campus, michael.raymer@wright.edu Follow this and additional works at: http://corescholar.libraries.wright.edu/cse Part of the Computer Sciences Commons, and the Engineering Commons Repository Citation Krane, D. E., & Raymer, M. L. (2003). The Structure and Functions of Proteins.. http://corescholar.libraries.wright.edu/cse/386 This Presentation is brought to you for free and open access by Wright State University s CORE Scholar. It has been accepted for inclusion in Computer Science and Engineering Faculty Publications by an authorized administrator of CORE Scholar. For more information, please contact corescholar@www.libraries.wright.edu.

BIO271/CS399 Bioinformatics The Structure and Functions of Proteins

The many functions of proteins Mechanoenzymes: myosin, actin Rhodopsin: allows vision Globins: transport oxygen Antibodies: immune system Enzymes: pepsin, renin, carboxypeptidase A Receptors: transmit messages through membranes Vitelogenin: molecular velcro And hundreds of thousands more Protein Structure and Function 2

Complex Chemistry Tutorial Molecules are made of atoms! There is a lot of hydrogen out there! Atoms make a preferred number of covalent (strong) bonds C 4 N 3 O, S 2 Atoms will generally pick up enough hydrogens to fill their valence capacity in vivo. Molecules also prefer to have a neutral charge Protein Structure and Function 3

Biochemistry In the context of a protein Oxygen tends to exhibit a slight negative charge Nitrogen tends to exhibit a slight positive charge Carbon tends to remain neutral/uncharged Atoms can share a hydrogen atom, each making part of a covalent bond with the hydrogen Oxygen: H-Bond donor or acceptor Nitrogen: H-Bond donor Carbon: Neither Protein Structure and Function 4

Proteins are chains of amino acids Polymer a molecule composed of repeating units Protein Structure and Function 5

Amino acid composition Basic Amino Acid Structure: The side chain, R, varies for each of the 20 amino acids Side chain H H Amino group N R C α H C O OH Carboxyl group Protein Structure and Function 6

The Peptide Bond Dehydration synthesis Repeating backbone: N C α C N C α C O O Convention start at amino terminus and proceed to carboxy terminus Protein Structure and Function 7

Peptidyl polymers A few amino acids in a chain are called a polypeptide. A protein is usually composed of 50 to 400+ amino acids. Since part of the amino acid is lost during dehydration synthesis, we call the units of a protein amino acid residues. carbonyl carbon amide nitrogen Protein Structure and Function 8

Side chain properties Recall that the electronegativity of carbon is at about the middle of the scale for light elements Carbon does not make hydrogen bonds with water easily hydrophobic O and N are generally more likely than C to h-bond to water hydrophilic We group the amino acids into three general groups: Hydrophobic Charged (positive/basic & negative/acidic) Polar Protein Structure and Function 9

The Hydrophobic Amino Acids Proline severely limits allowable conformations! Protein Structure and Function 10

The Charged Amino Acids Protein Structure and Function 11

The Polar Amino Acids Protein Structure and Function 12

More Polar Amino Acids And then there s Protein Structure and Function 13

Planarity of the peptide bond Psi (ψ) the angle of rotation about the Cα-C bond. Phi (φ) the angle of rotation about the N-Cα bond. The planar bond angles and bond lengths are fixed. Protein Structure and Function 14

Phi and psi φ = ψ = 180 is extended conformation φ : Cα to N H ψ : C=O to Cα Cα N H C=O Protein Structure and Function 15

The Ramachandran Plot Observed (non-glycine) Calculated Observed (glycine) G. N. Ramachandran first calculations of sterically allowed regions of phi and psi Note the structural importance of glycine Protein Structure and Function 16

Primary & Secondary Structure Primary structure = the linear sequence of amino acids comprising a protein: AGVGTVPMTAYGNDIQYYGQVT Secondary structure Regular patterns of hydrogen bonding in proteins result in two patterns that emerge in nearly every protein structure known: the α-helix and the β-sheet The location of direction of these periodic, repeating structures is known as the secondary structure of the protein Protein Structure and Function 17

The alpha helix φ ψ 60 Protein Structure and Function 18

Properties of the alpha helix φ ψ 60 Hydrogen bonds between C=O of residue n, and NH of residue n+4 3.6 residues/turn 1.5 Å/residue rise 100 /residue turn Protein Structure and Function 19

Properties of α-helices 4 40+ residues in length Often amphipathic or dual-natured Half hydrophobic and half hydrophilic Mostly when surface-exposed If we examine many α-helices, we find trends Helix formers: Ala, Glu, Leu, Met Helix breakers: Pro, Gly, Tyr, Ser Protein Structure and Function 20

The beta strand (& sheet) φ 135 ψ +135 Protein Structure and Function 21

Properties of beta sheets Formed of stretches of 5-10 residues in extended conformation Pleated each Cα a bit above or below the previous Parallel/aniparallel, contiguous/non-contiguous Protein Structure and Function 22

Parallel and anti-parallel β-sheets Anti-parallel is slightly energetically favored Anti-parallel Parallel Protein Structure and Function 23

Turns and Loops Secondary structure elements are connected by regions of turns and loops Turns short regions of non-α, non-β conformation Loops larger stretches with no secondary structure. Often disordered. Random coil Sequences vary much more than secondary structure regions Protein Structure and Function 24

Levels of Protein Structure Secondary structure elements combine to form tertiary structure Quaternary structure occurs in multienzyme complexes Many proteins are active only as homodimers, homotetramers, etc.

Protein Structure Examples Protein Structure and Function 26

Views of a protein Wireframe Ball and stick Protein Structure and Function 27

Views of a protein Spacefill Cartoon CPK colors Carbon = green, black, or grey Nitrogen = blue Oxygen = red Sulfur = yellow Hydrogen = white Protein Structure and Function 28