How many carbon atoms are present in the R group in each of the following standard amino acids? 3-10 a. b. COOH OH CH2 CH H,N--C-COOH H2N-C-COOH H H d. CH3 с. CH3 CH2 CH--OH CH--CH3 H,N-C--COOH H2N-C-COOH H. H.
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How many carbon atoms are present in the R group in each of the following standard amino acids? Please see picture. Thank you!
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- 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 -0The structure of the dipeptide Gly-Asn is given by . The structures of the amino acids Gly and Asn are given below. NH2 H. ČH2 H3N-C-CO H. H3N-C-CO H. Asn Gly NH2 CH2 H H H2 C COO 2. H3N-C -C H. 1. H&N C C-NH C COO NH, NH2 CH2 H. H2 C C NH2 3. H3N-C C- -C COO 4. 0OC-C NH3" Click Save and Submit to save and submit. Click Save All Ansuwers to save all answers. MacBook Air esc 吕0 DII DD F1 F2 F3 F4 F5 F6 F7 F8 F9 @ 2$ & 1 2 4 5 7 8 Q W E R Y | A S D F G K C V N M < CO # 3 HICHShown below are three amino acids: H,N-CH-C-o ҫн, H,N-CH-C-o CH, H,N-CH-C-o ČH, Tyrosine Tyr Y Phenylalanine Phe F Alanine Ala A 1. Which amino acid is the least hydrophobic? 2. Which amino acid is most hydrophobic? 3. Which amino acid is intermediate? 4. Explain why (2) is more hydrophobic than (3). 5. Explain why (3) is more hydrophobic than (1).
- Which of these amino acids is a basic amino acid? (Select all that apply, if necessary.) A. B. C. D. O MNCHI MCHEⓇ || H₂N- H₂N- CH-C- CH₂ CH₂ CH₂ C=O CH₂ Oe NH + C=NH2 NH₂ amino acid E amino acid D amino acid A amino acid B amino acid C H₂N-CH- CH₂ T CH₂ C=O T NH₂ H₂NⓇ 용_。 CH₂ CH-CH3 CH3 E. H₂N-CH-C-0 CH₂ OHWhich of these amino acids is an acidic amino acid? (Select all that apply, if necessary.) B. C. D. A. H₂ND CH-&- H₂ND H₂ND CH-1 CH₂ CH₂ CH-CH3 C=O I CH3 оӨ H₂N- -CH-C I CH₂ CH₂ CH₂ NH + C=NH2 NH₂ amino acid D amino acid C amino acid E amino acid B amino acid A O H₂N-CH-C- CH₂ T CH₂ C=0 NH₂ E. His H₂N-CH-C CH₂ ОНIn the following scheme: HH, H₂C-C-C-Coo II HO H • NH, 1 H₂C-C-C-C000 H 2-Amino-3-ketobutyrate ↓ O H,C-C-CH₂-NH₂ Aminoacetone 0 0 H₂C-C-C-H Methylglyoxal H H₂C-C-COO OH D-Lactate O H₂C-C-C000 Pyruvate What molecule is being metabolized? Identify the reaction at each step. If it is an oxidation-reduction prove this is correct by showing oxidation state changes on the atoms in the structure.
- 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) HBelow are two amino acids at physiological pH. Number labels are for part c. Answer the following questions about the side chains of these amino acids. H C. H;N* 2 CH2 A H H3N* C 3 CH2 В 4он В a. Which amino acid has a polar side chain? b. Which amino acid is more soluble in water? B c. Select the atom that serves as the hydrogen bond donor in the amino acid's R group.Exercise A: Amino Acid Functional Groups Figure 1 below shows one of the 20 amino acids that make up proteins. Recall that carbon can form four covalent bonds. Amino acids consist of a central carbon, called the a-carbon, that is bonded to four different chemical groups. H + CH2 OH Figure 1. Structure of an amino acid Answer the below questions in your own document. • On the amino acid shown in Figure 1, label the a-carbon. • The a-carbon of each of the 20 amino acids is bonded to one hydrogen atom, one amino group, one carboxyl group, and one R group (more on that below). You should recognize the amino and carboxyl groups from our discussion of functional groups in organic molecules. Circle and label* the amino group and the carboxyl group in Figure 1. *Note: our goal in this question, and in similar questions throughout this lab, is for you to be able to identify specific structures. You can do this circling/labeling in whatever way is easiest for you. You might want to draw the…
- In the following list, identify the carbohydrate, the fatty acid, the amino acid, and the polypeptide:a. methionine-valine-proline-leucine-serineb. C6H12O6c. NH2CHRCOOHd. CH3(CH2)16COOHPlease 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 ноIdentify 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