In the peptide shown below, a covalent bond that could rotate to form secondary structureis correctly identified / labeled by letter:ABOHstill fotDOBOCOOOBDFCOAHNENHOH"NH₂- F

There are two types of secondary structures are which are found in protein: alpha helix and beta…

Answered: In the peptide shown below, a covalent…

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

If the protein you are studying is known to bind the molecule shown below, what types of amino acids would you expect to be forming interactions at each of the numbered positions. Explain your reasoning for your choices 2 0 N* H- H H. 4. 3. 1,
Rank these amino acids from most to least hydrophobic. H #3 13N-C-H CH₂OH 1 Q .000 OB) 3>2 > 1 E D A) 1>3>2 C) 3 >1 > 2 $ 4 R F % 5 coo™ H₂N-C-H T + __8_5 A CH 2 CH₂ CH₂ 3 2 6 CH MacBook Pro Y & 7 G | H U * 00 8 J 1 + _000 H₂N-C-H CH ₂ 1 CH₂ _000 9 3 K O 0 L d
Which of the numbered bonds in this polypeptide fragment are peptide bond(s)? (Select all that apply!)
Identify each of the amino acid in the polypeptide and then name it using the 3-letter abbreviations.
Identify an amino acid that complies with the following characteristic: (VWrite the COMPLETE name) Contains a side chain with a thioether bond
Name the following nucleotide.
The structure given is NH OH 'N' HO-P=0 ÓH A uridine monophosphate deoxycytidylate C thymidylic acid uridylate
Which of these amino acids is a hydrophobic amino acid? (Select all that apply, if necessary.) A. B. C. D. E. iº H₂N-CH-C CH₂ T CH₂ CH₂ NH C=NH2 NH₂ amino acid E amino acid D amino acid B amino acid C amino acid A 200 H₂N-CH-C CH₂ C=O I OO H₂N-CH-C- CH₂ CH₂ T C=O T NH₂ 0 H₂N-CH- CH₂ CH-CH3 CH3 H₂N-CH-C CH₂ I OH -0
I-D-E-L-Y-S-Q-V-C-S-H-L-D-T-V-R Circle the hydrophobic residues in the amino acid sequence above and box the hydrophobic residues.
Identify the amino acid: pic 2.png Tryptophan Asparagine Histidine Proline
Create an oligopeptide via dehydration synthesis using the following amino acids. O. H Tryptophan (TRP) C-C-N но сн, C-C-N. но Glycine (GLY) H H HN
Which of the following best describes how the secondary structure of a protein is formed? A B с D O=U a-helix H O=C N-H R-C-H C=0 H-N H-C-R O=C N-H R-C-H C=O H-N O-C N-H R-C-H C=O H-N N-H 0= H-C-R H-N C=O R-C-4 N-H O=C H-C-R 4-1 Ç=O R-C-H N-H 0=C H-C-R (=O R-C-H B-pleated sheet ionic bonds between the R groups of the polypeptide amino acids -Uh hydrogen bonds between the carboxyl and amino groups of non-adjacent amino acids covalent bonds between the carboxyl and amino groups of adjacent amino acids hydrogen bonds between the R groups of the polypeptide amino acids

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In the peptide shown below, a covalent bond that could rotate to form secondary structure is correctly identified/labeled by letter: B E OH Thil fond OE OC B D C OF OA D HN NH OH "NH₂ F