Classify each of the amino acids below.Note for advanced students: none of these amino acids are found in normal proteins.+H3N-CH-COOH3NCH-COOH3NCH COOCH2CH NH3CH2SCH2CH3CH3(Choose one)(Choose one)(Choose one) ▼nonpolarpolar neutralH3N—CH CAO HƠN CHCOOpolar acidicpolar basicCH2COOCH2CH2H3CCH3NH2(Choose one)(Choose one)(Choose one)

Certainly! Amino acids, the building blocks of proteins, are typically classified by the properties…

Answered: Classify each of the amino acids below.…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Similar questions

Identify the amino acid shown below. (Note: single letter code is provided as answer) H H₂N-C-COOH CH₂ CH₂ S CH₁ M Ow F Oc
A protein that is normally found in an aqueous solution has these amino acids in its primary structure: glutamic acid, lysine, leucine, arginine, and tryptophan. Predict the location of each amino acid: in the interior portion of the protein (away from water) or on the outside of the protein (facing water). glutamic acid _________________________ lysine _________________________ leucine _________________________ arginine ________________________ tryptophan _________________________ Indicate whether each of the following statements describes a reversible competitive inhibitor, reversible noncompetitive inhibition, or an irreversible inhibitor. ________ a. It bonds covalently to the active site ________ b. The inhibitor effect can be reversed by the addition of more substrate ________ c. Inhibitor structure resembles that of the substrate ________ d. The inhibitor and substrate cannot bind to the enzyme simultaneously.
A protein that is normally found in an aqueous solution has these amino acids in its primary structure: glutamic acid, lysine, leucine, arginine, and tryptophan. Predict the location of each amino acid: in the interior portion of the protein (away from water) or on the outside of the protein (facing water). glutamic acid _________________________ lysine _________________________ leucine _________________________ arginine ________________________ tryptophan _________________________
Many bioactive compounds are derived from amino acids. This compound, found in trace amounts in mammalian brains and hypothesized to play a role as a neuromodulator or neurotransmitter, is derived from an amino acid through removal of the backbone carboxylic acid group. The amino acid from which it is derived must be: (Write out the entire name; Spelling matters, but case does not; Do not include L- or D- in the name; For acidic amino acids write the full name, e.g. “so-and-so acid”)
Use circles to represent amino acids in the polypeptide shown below. OColor each amino acid using the color scheme: polar, basic amino acid = blue; polar acidic amino acid = red; non-polar amino acid = yellow H3N*-ala-ile-trp-arg-gly-ala-his-tyr-trp-gly-gly-tyr-arg-ile-val-thr-ile-trp-cys- met-gly-ile-asp-cys-thr-glu-cys-trp-gly-cys-phe-arg-his-pro-val-phe-Co-
Identify the nonpolar amino acids and the acidic aminoacids in the following peptide:Glu-Thr-Val-Asp-Ile-Ser-Ala
Write down the abbreviations (both 1 letter and 3 letter) for the amino acids given below:Tryptophan, Glutamine, Isoleucine, Cysteine, Arginine
Please clearly identify each numbered amino acid side chain, below. Your description should include the name or 3 letter code for the amino acid and the type (i.e., chemical class) of the amino acid. 1 4 OH OH CH, CH, CH2 CH2 CH, "H,N-C-C-0 "H,N-C-C-0 "H,N-C-C-0 _0-5-5-N H. H O H O HO но
Select the choice that best describes the stereochemistry of the following amino acid, and rank the priority of the four groups surrounding the alpha carbon (in DESCENDING order: 1-highest 4-lowest) NH₂ CO₂II CH₂SH Cysteine H D and S, (1-NH2, 2-CH2SH, 3-COOH, 4-H) Land R, (1-NH2, 2-COOH, 3-CH2SH, 4-H) OL and R, (1-NH2, 2-CH2SH, 3-COOH, 4-H) D and S, (1-CH2SH, 2-COQH, 3-NH2, 4-H) H
For the protein given in the attached picture: Write the name of these 5 amino acids corresponding to their abbreviation of 3 letters. Describe precisely how the functional groups in the amino acids are involved in bonding between two successive amino acids in the protein.
Provide the correct three-letter abbreviation for the following amino acid: O || H₂N-CH-C-OH I CH₂ CH₂ C=O I NH₂
Fill out the related information for all three amino acids in the chart. On a separate piece of paper provide calculations for all pl values; one a-amino group; one a-carboxyl group and all the ionizable R-groups. pKa table provided. pH = pKa + log (cb/ca)

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