Protein synthesis is which type of reaction? Group of answer choices A. ester synthesis is anabolism B. ester synthesis is catabolism C. amide synthesis is catabolism D. amide synthesis is anabolism Triglyceride synthesis is which type of reaction? Group of answer choices A. amide synthesis is anabolism B. amide synthesis is catabolism C. ester synthesis is catabolism D. ester synthesis is anabolism

Protein synthesis is which type of reaction? Group of answer choices A. ester synthesis is anabolism B. ester synthesis is catabolism C. amide synthesis is catabolism D. amide synthesis is anabolism Triglyceride synthesis is which type of reaction? Group of answer choices A. amide synthesis is anabolism B. amide synthesis is catabolism C. ester synthesis is catabolism D. ester synthesis is anabolism

Anatomy & Physiology

1st Edition

ISBN:9781938168130

Author:Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark Womble

Publisher:Kelly A. Young, James A. Wise, Peter DeSaix, Dean H. Kruse, Brandon Poe, Eddie Johnson, Jody E. Johnson, Oksana Korol, J. Gordon Betts, Mark Womble

Chapter24: Metabolism And Nutrition

Section: Chapter Questions

Problem 1RQ: A monosaccharide is formed from a polysaccharide in what kind of reaction? oxidation-reduction...

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adenine molecule ii. NH2 N- НО-Р—О—Р—О—Р—О. ОН ОН ОН i. Phosphate chain ОН ОН iii ribose sugar
Small molecules are used as inhibitors of protein action - as drugs. They most often do this by blocking the active site within the protein. Potential drugs can be screened computationally to determine if they are strongly bound to the protein. Figure 1 shows a possible conformation of a candidate drug molecule, 4-bromo-2- carboxymethylamide-pyrrole (abbreviation: BCMAP) at the active site of a protein (abbreviation: PR). Figure 2 shows the full protein structure whilst figure 3 shows a known inhibitor of the protein at the site, overlayed with another calculated conformer of BCMAP. (c) Outline how you would investigate whether BCMAP would be an effective inhibitor for the protein in competition with the molecules that the protein normally targets, and any solvent. Figure 1. 4-bromo-2-carboxymethylamide-pyrrole (BCMAP) (C, N, O, and Br atoms in yellow, blue, red, and brown, respectively) in the active site of the protein structure.
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FIGURE 6 substrate active site enzyme substrate denatured enzyme substrate cannot enter binding site 3 C enzyme products leaving active site substrate denatured enzyme 13. Figure 6 above shows what happens to an enzyme when exposed to heat. How is this similar to what happened to my crayons? 14. What term is used to describe when the shape of the enzyme has been altered? (Look at the figure in the middle!) 15. Can you predict other things that may influence the activity of enzymes in a positive or negative way?
Which of the followinga.B-D-riboseb. thyminec. phosphatewhich is not a component of deoxyribonucleotide?
out of 20 ..amino acids, identify the one that ..has a side chain that reacts with HCl via acid base reaction
______ 1. is a serine protease that cuts the peptide after aromatic amino acids______ 2. is a type of chemical bond formed by chymotrypsin with its substrate as a first step in the reaction mechanism______ 3. is the name of the compound that hydrolyzes the chemical bond formed between chymotrypsin and its substrate ______ 1. is the name of the inactive form of chymotrypsin
8. The chemical structure of Coenzyme A contains the following except— a phosphoanhydride moiety. a β-mercaptoethylamine residue. a lipoic acid residue. a pantothenic acid residue. an adenosine-3’- phosphate.