protein backbone for any amino acid residues from exercise 4 that are capable.6. For each of the following representations (from OpenStax Biology), indicate whether it isdescribing primary, secondary or tertiary protein structurea.OHH RHARICHOHH R OHH ROHHC-NCC-NCC-NCC-NCC-NH HRHHA ARRHHORCCN_C_CONHHOCCN-C CON-C CN-CHHC=OHITIRHFRH HOR HCN-CCN-C CN-C CN-C CN-CREH-NRICHQ=0b.Gly Ser His Leu Val Glu Ala Leu Tyr Leu ValasSC.

Let's break down each of the representations and explain whether they describe primary, secondary,…

Answered: protein backbone for any amino acid…

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...

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Similar questions

23. The amino acid side chains of 17 of the 20 most common amino acids are shown below. Which are aromatic side chains? Type their corresponding letter in alphabetical order.
Current What type of interaction would you expect between the following R groups of a protein? CH3 and CH2 O hydrophobic interactions O hydrogen bonding O disulfide bond O salt bridge
Which of the following amino acids is polar acidic? OH CH3 CH, H-C-OH H,C CH-C-0 NH H-N-C-C-0 H,N-C-C-O H O но C=CH CH2 CH, H3N*-C-C-O- H,N-C-C-o H O H O a b. C. e O a O b O d O e
Researchers discover a new amino acid. Its R-group exclusively has hydrogen and carbon atoms. What behavior will this amino acid show? O Relative to the amino acids found in organisms, its interactions with water will be very high. It is hydrophilic. Relative to the amino acids found in organisms, its interactions with water will be intermediate. It is hydrophobic.
Which of the following is the correct structure for Ser-Ala-Asp? The appropriate side chains look like this. Ala -CH3: Ser -CH₂-OH; Asp -CH2-C-OH O O CH ₂0 1 11 0 OH 1 Top CH2 O 1 11 111 +H_N-CH-C-NH-CH-C-NH-CH-CO- COOH COOH 1 CH) Ổ 11 +H_N-CH-C-NH-CH-C-NH-CH-CƠ 1 CH2 O +H₂N-CH OH 1 CH2 O 0 COOH COOH 1 CH 20 OH 1 CH2 O 1 CH2 O CH, O II CH, O ||||| I - C -NH-CH-C-NH-CH-CO- OH T CH2O #TI CH₂0 +H_N-CH-C-NH-CH-C-NH-CH-CO- COOH
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
Q2
Identify the features of the two bonded amino acids depicted in the image. HOHH | || | | N-C-C-N-C-C CH CH₂2 CH₂2 CH₂ CH₂ I I CH₂ CH₂ NH₂+ O OH Answer Bank hydrophilic side chain hydrophobic side chain peptide bond carboxyl group amino group
This amino acid would be more likely to bind to a receptor inside of the cell. COO- H3N-C-H CH2 CH2 CH2 CH2 *NH3 True O False This amino acid would be more likely to bind to a receptor inside of the cell. COO H3N-C-H H-C-CH3 CH2 CH3 O True O False
Name the following amino acids using their common name
DF eas fil PDF e UNOFFIC TRANSCR 59°F Mostly cloudy CH3 Classify the amino acid with the R group -CH₂-CH-CH3 according to its polarity. O polar, acidic O polar, neutral O polar, basic O nonpolar 10 4 % M LO 5 10 6 7 os hp 4+ 8

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