The image depicts a molecular structure diagram of a polypeptide segment. Key functional groups in the structure include alpha carbon, R groups, and peptide bonds. The instructional text at the top reads:"Drag the appropriate labels to their respective targets. Labels can be used more than once."To the left, there is a list of labels:- α carbon- R group- peptide bondThe molecular diagram in the center shows a sequence of amino acids with highlighted areas meant for label placement. Chemical groups include:1. An amino group $(\text{H}_3\text{N}^+\text{--CH--CO--NH--CH}_2)$ with a phenol ring as an R group.2. A central carbon marked with potential label boxes.3. Peptide bonds between amino acids shown as $\text{C--NH--CH}$ links.4. Several side chains indicating different R groups: - A phenyl ring with an OH group. - A group with $\text{CH}_2\text{OH}$. - A group with $\text{CH}_2(\text{CH}_2)_2\text{NH}_3^+$.The structure involves typical peptide bonds linking amino acids and a variety of side chains characteristic of different R groups in proteins.The bottom of the diagram has 'Reset' and 'Help' buttons, suggesting an interactive component for educational purposes.

Given molecule is peptide. Which formed by peptide bond . From alpha amino acids. Peptide bond is…

Drag the appropriate labels to their respective targets. Labels can be used more than once. Reset Help a carbon HÑ-CH- -NH-CH-Č NH-CH CH2 CH,OH R group peptide bond OH 梦 $ * 4:19 PM 71F A G E D 40 10/10/20 立

Drag the appropriate labels to their respective targets. Labels can be used more than once. Reset Help a carbon HÑ-CH- -NH-CH-Č NH-CH CH2 CH,OH R group peptide bond OH 梦 $ * 4:19 PM 71F A G E D 40 10/10/20 立

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: The above is the structure of a ___ pentapeptide? Basic Acidic Neutral

A: The above pentapeptide structure is basic.

Q: Would you expect this amino acid to be found at the surface or the centre of a water-soluble…

A: Hydrophilic: This type of organic compound contains polar or ionic groups so that they are soluble…

Q: Choose the set of letters corresponding to the BEST answer. -OH -OH -OH H₂N- CH- 151 +4 CH₂ HN H₂N-…

Q: 9. How do you know if a malenimide based reagent will conjugate to nitrogen or sulphur in an amino…

A: we can identify the malenimide based reagent as amino acids by looking at the following - amino…

Q: Which of the following amino acid side chains can help remove a proton from the a-carbon of an…

A: The carbon atom which is present just adjacent to the carbonyl group in aldehyde and ketone is…

Q: (a) Which of the common amino acids have more than one carboxyl group?

A: Amino acids having more than one carboxylic acid (-COOH) group are acidic amino acids.

Q: What bonding/interaction(s) is possible between octane derivatives and peptides? O Cation-to-Anion O…

Q: Tyrosine, Tyr, Y coot 1 8P + PO - соо H₂N-C-HH3N"-"C-H = H₂N-C-H CH₂ 1 CH₂ PH-Pha= 2.20 OH (+1) CONS…

A: The isoelectric point of an amino acid is the pH at which the amino acid has a neural charge...

Q: 4. Draw structures for 8-amino-5,7-dicyclopropyldecanal cis-8-amino-5,7-dicyclopropyldeca-3,9-dienal…

A: Given IUPAC names are a) 8-amino-5,7-dicyclopropyldecanal b)…

Q: 80. Determine whether each statement is true or false. If false, correct it. (a) The Fe2+ ion…

A: The charge within an atom or molecule has always been determined by the number of protons and…

Q: 2- What are the net charges of the following AA's at the pH-Values of (1, 5, 7, and 11.0)? Show the…

A: The net charge on the amino acid will change depending on the pH value because, the ionizable groups…

Q: Modify the structures (if necessary) to show the predominant form of the amino acid tyrosine at each…

Q: Proteins are made from chains of amino acids. The amino acids are joined together by structures…

A: The structure of the dipeptide that is formed from two glycine molecules at the pH of most body…

Q: What are the predicted products when Ca(OH)2 dissociates in water? Group of answer choices Ca2+ +…

A: We have to predict products when Ca(OH)2 dissociates in water as follows in step 2:

Q: The following structure is cimetidine. The guanidine moiety at the end of the side chain is neutral.…

A: In the structure of cimetidine, the guanidine moiety at the end of side chain is indeed neutral…

Q: more polar to less polar compunds

A: In this question we have to give rank from more polar to less polar compounds with explanation.

Q: 2. What is the correct IUPAC name of a molecule in the box? NH2 ÓH O 1-hydroxy-3-amino-2-propanone…

A: The given compound: It contains 3 carbon atoms in the main chain. It has one amino group and one…

Q: Consider the hypothetical serine protease in the image, which shows the specificity pockets. The S,…

A: Hydrophobic side chains are non-polar side chains. The hydrophilic side chains are polar, acidic,…

Q: 01 02 03 04 10--0 НО 2 2x OH HO OH OH O HO OH OH OH

Q: Imagine the main chain of a protein bends back on itself, so that two amino acid residues R, and R₂…

A: Certainly! Let's delve into the interactions between amino acid residues.1. Valine (R) and…

Q: Q1.Fill in positive, negative and neutral The isoelectric point, pl, of two amino acids is shown…

Q: - Alanine has pK, values of 2.34 and 9.60. At what pH will alanine exist in the indicated form? of…

A: Alanine with overall negative charge and 50 % of zwitterion is possible at the pH of 9.60. At pH of…

Q: Given below is the structure of a peptide with the name seryllysylaspartate. What is the amino acid…

A: The amino acid present at C-terminal of given peptide is : A peptide has two terminals, one is…

Q: ogical Marcomalee Identifying specific interactions between residues in a protein Imagine the main…

A: The formation of hydrogen bonds is an essential component in the process of preserving the…

Q: Choose the structure that best represents the following amino acid at pH = 2. О А . NH3 A ОН ASH NH₂…

A: At pH = 2, -NH2 exists as -NH3+ and -COOH exists at -COOH

Q: Identify one amino acid from each of the following categories: H2N CH-C-OH H2N-CH-C-OH H,N-CH- -OH…

A: There are 20 known naturally occurring amino acids. An amino acid is an organic molecule which has…

Q: + Question 16 of 20 Provide the correct three-letter abbreviation for the following amino acid: Gln…

Q: The isoelectric point of a polypeptide or protein is equal to the pH at which the overall charge is…

A: We know if the pH is greater than pka, then deprotonation occurs and it exists in deprotonated form.…

Q: The net charge on the following amino acid is [x] at pH 10. HS NH₂ ОН

A: Given is amino acid.The name of given amino acid is cysteine.

Q: protein. O H H " H₂N-CH-C-N-CH-C-O O || I CH3 Ala Arg Asn Asp Cys Glu Gln Gly His lle Leu Lys

Q: Highlight each peptide bond in the molecule below. In addition, list the common names of the smaller…

A: The chemical bonds that bind amino acids together to make proteins are known as peptide bonds. They…

Q: CH3C-N carboxylic acid CH3C-OH ester CH3COČCH, anhydride CH2CH2CHÔNH2 amide ČH,CH3 CH,CH2CHC осн…

A: Functional group are the substitutents or group of atoms which will impart the specific chemical…

Q: Which structure below contains a peptide bond? H2N FHÇ- H N- CH3 O CH3 H2NFCH- С— ОН CH3 H2N-CH2-C-…

A: A peptide bond is formed from the reaction of a carboxylic group with an amine group through the…

Q: 21. The melting points (mp) of three beta agonist homologues are given below OH HO. ОН Terbutaline…

A: The objective of this question is to show the expected order of solubility of water from lowest to…

Q: Highlight each peptide bond in the molecule below. In addition, list the common names of the smaller…

A: Peptide bond is an amide type of covalent bond.

Q: What is the single-letter code of the primary sequence for our favorite peptide below? NH₂ Fo NH₂ HO…

A: Given is peptide molecule.Peptide are consist of amino acids.There are three and one letter codes…

Q: eck the box under each a amino acid.

A: Given are organic compounds. Amino acids are compounds that contain two functional groups carboxylic…

Q: |回新建标| My file W Docum W 2.14- - i (4 x E O F A Table c b Answe W Scurvy Gramn V My Cit Q Detern Q…

Q: s peptide bond 2 (colored red) drawn cis or trans? O trans Ocis NH₂ SH III NH 1 o= HN OH HN 3 o= CH3…

A: The objective of the question is to predict whether the peptide bond 2 is cis or trans.

Q: How many peptide bonds do you see in the following structure?

A: A question based on amide. For the given question, the number of peptide bonds available has to be…

Q: Pb + 2e" Pb E° = -0.13 V "Aga) +e Ag) E° = +0.80 24 The c.m.f of the cell is (A) +0.93 V (C)-0.67 V…

A: Hey, since there are multiple questions posted, we will answer first question. Kindly request other…

Q: Highlight each peptide bond in the molecule below. In addition, list the common names of the smaller…

A: The question is based on the concept of biomolecules.We have to identify the bonds and write the…

Q: Draw the structure of the peptide WAKEP. Write the full name of each amino acid above the relevant…

A: Here we are required to find the net charge over the peptide WAKEP.

Question

The image depicts a molecular structure diagram of a polypeptide segment. Key functional groups in the structure include alpha carbon, R groups, and peptide bonds. The instructional text at the top reads:

"Drag the appropriate labels to their respective targets. Labels can be used more than once."

To the left, there is a list of labels:
- α carbon
- R group
- peptide bond

The molecular diagram in the center shows a sequence of amino acids with highlighted areas meant for label placement. Chemical groups include:

1. An amino group $(\text{H}_3\text{N}^+\text{--CH--CO--NH--CH}_2)$ with a phenol ring as an R group.
2. A central carbon marked with potential label boxes.
3. Peptide bonds between amino acids shown as $\text{C--NH--CH}$ links.
4. Several side chains indicating different R groups:
- A phenyl ring with an OH group.
- A group with $\text{CH}_2\text{OH}$.
- A group with $\text{CH}_2(\text{CH}_2)_2\text{NH}_3^+$.

The structure involves typical peptide bonds linking amino acids and a variety of side chains characteristic of different R groups in proteins.

The bottom of the diagram has 'Reset' and 'Help' buttons, suggesting an interactive component for educational purposes.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Similar questions

Macmillan Learning COO™ addition of a hydroxyl group -OOC-CH-CH₂-CH-COO 1 *NH₂ ✓addition of a carboxyl group modification of the a-amino group removal of a side chain amino group removal of a -CH group standard amino acid: Identify the modification that yields the second amino acid depicted. addition of a carboxyl group Glutamic Acid
[References] For each structure on the left, pick an identification on the right. Clear All H,N CH- CH- CH2 amino acid dipeptide HO-C-(CH2-C-CH dicarboxylic acid NH2- (CH-)6 NH2 diamine OH HN CH
Highlight each peptide bond in the molecule below. In addition, list the common names of the smaller molecules that would be released if all the peptide bonds were hydrolyzed. You can add more rows to the table if you need to. (Note: you do not need to list water.) If there are no peptide bonds in the molecule, just check the no peptide bonds box below the drawing area. Ono peptide bonds Add Row I Don't Know H₂N-C Submit CH₂ CH C–NH–CH—CO0 CH, CH3 molecules released if peptide bonds hydrolyzed (list one name per row) 0 CH3 00 X S X 3 alo Ar © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accessibility
@ 2 Draw the amide formed when 1-methylethylamine (CH₂CH(CH3)NH₂) is heated with each carboxylic acid. W 5 X 25,248 CH,CH,CH,COOH + CH,CH(CH,)NH, -> # 3 E D C G MAR 28 $ 4 R F V % 5 G Search or type URL T G B Reaction A tv ♫ < 6 Select Draw Templates More Y MacBook Pro / |||||| C H N H 3 & 7 N U NIDZA J * 00 8 + M I M - 9 0 K A < ܀܀ O < ) Q2 Q O L W ◄» P command ^. Erase T Aa { + [ = option "F
X + Dashboard X app.101edu.co Aktiv Chemist X Question 20 of 20 Hydrogenation X Provide the correct one-letter abbreviation for the following amino acid: H3N-CH-C-0 H A Q G R N D C E HILK G What set of w X ☐ Sun Apr 16 6:47 PM DOCX + Update: Submit
What is the conjugate acid of the following bases? 4) HSO41- 5) H2PO41- 6) C5H5N
3gth356g/vewform?edit requested Fw751UyNbHc3H 61 This is called HO но. COOH Iinolec acid salicylic acid phenolpthalein 62. The structural formula below is a/an NH2 amide amine ester O O O
The shaded area in the following diagram shows CH₂ CH | H CO-H-N N-H-O -CH₂ C-OH-N Gly 193 H RN Covalent bond formation between a catalytic amino acid residue and the substrate during chymotrypsin catalysis. Acid-base catalysis by a catalytic residue in chymotrypsin. Oxyanion hole which stabilizes substrate binding in chymotrypsin catalysis. Oxyanion hole which stabilizes transition state in chymotrypsin catalysis. Low barrier hydrogen bond formation between the transition state and one of the catalytic residues of chymotrypsin. ?
Modify isoleucine to show its structure at pH 1 and pH 13. Modify each amino acid by adding or removing atoms or bonds and by adding charges where appropriate. pH 1 pH 13 Select Draw Rings More Erase Select Draw Rings More Erase H N H N CH, CH, CH, CH, H,C - CH H,C - CH H,N C- 0 - H - H,N - C - C- 0 - H II H.
Phenol plus 1) 1/2 I2, HNO3; 2) Br2 + AlCl3; 3) HNO3/H2SO4; can yield ___________. 2-bromo-6-iodo-4-nitrophenol 1-bromo-3-iodo-4-amino-phenol 3-bromo-5-iodo-4-nitrobenzene 2-bromo-3-iodo-4-hydroxy-aniline 2-bromo-3-iodo-4-nitrophenol
Q3- We wish to synthesize all possible dipeptides containing the amino acids tyrosine, lysine, phenylalanine, and leucine. Identify the number of possible dipeptides and explain how we would carry this out using combinatorial techniques.
H + H3N- C In the amino acid shown here, what is the identity of the highlighted unit? O || -C-O Question 30 of 30 CH₂ CH₂ C=O NH₂ A) alpha-carbon B) alpha-carboxyl group C) alpha-amino group D) side chain R-group Submit +