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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 vere hydrolyzed. You can add more rows to the table if you need to. (Note: you do not need to list water.) f there are no peptide bonds in the molecule, just check the no peptide bonds box below the drawing area. H₂N-CH- CH CH CH3 11C -C- NH-CH-COO H₂N CH₂ CH₂ CH, NH ΝΗ, X ? Olo Ar

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 vere hydrolyzed. You can add more rows to the table if you need to. (Note: you do not need to list water.) f there are no peptide bonds in the molecule, just check the no peptide bonds box below the drawing area. H₂N-CH- CH CH CH3 11C -C- NH-CH-COO H₂N CH₂ CH₂ CH, NH ΝΗ, X ? Olo Ar

Human Anatomy & Physiology (11th Edition)
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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**Instructions:** Highlight each peptide bond in the molecule provided. Also, 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 needed. (Note: you do not need to list water.) If there are **no** peptide bonds in the molecule, check the "no peptide bonds" box below the drawing area. **Molecular Diagram Description:** The diagram represents a structural formula of a peptide showing the following: - A backbone consisting of alternating nitrogen (N) and carbon (C) atoms. - A terminal amino group (\( \text{H}_3\text{N}^+ \)) on the left linked to a C atom. - Two side chains branching off from the central carbon atoms: - The first side chain: \(\text{CH}_2\text{CH}_2\text{S}\text{CH}_3\) - The second side chain: \(\text{CH}_2\text{CH}_2\text{NH}\text{C(NH}_2)_2^+\) - Peptide bonds (\(-\text{C(O)NH}-\)) are connecting the backbone carbon and nitrogen atoms. - A terminal carboxylate group (\(\text{COO}^-\)) on the right. **Table:** _Check the box if the molecule has no peptide bonds._ **Molecules Released if Peptide Bonds Hydrolyzed:** (List one name per row)
Transcribed Image Text:**Instructions:** Highlight each peptide bond in the molecule provided. Also, 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 needed. (Note: you do not need to list water.) If there are **no** peptide bonds in the molecule, check the "no peptide bonds" box below the drawing area. **Molecular Diagram Description:** The diagram represents a structural formula of a peptide showing the following: - A backbone consisting of alternating nitrogen (N) and carbon (C) atoms. - A terminal amino group (\( \text{H}_3\text{N}^+ \)) on the left linked to a C atom. - Two side chains branching off from the central carbon atoms: - The first side chain: \(\text{CH}_2\text{CH}_2\text{S}\text{CH}_3\) - The second side chain: \(\text{CH}_2\text{CH}_2\text{NH}\text{C(NH}_2)_2^+\) - Peptide bonds (\(-\text{C(O)NH}-\)) are connecting the backbone carbon and nitrogen atoms. - A terminal carboxylate group (\(\text{COO}^-\)) on the right. **Table:** _Check the box if the molecule has no peptide bonds._ **Molecules Released if Peptide Bonds Hydrolyzed:** (List one name per row)
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