Consider this structure.CH₂OHHOPart 1 of 3NHIdentify the monosaccharide. Select the single best answer.D-2-deoxyriboseD-ribosePart 2 of 3Identify the base. Select the single best answer.thymineguaninecytosineadenineOuracilPart: 2/3Part 3 of 3Name the structure.хNH₂

Ribose sugar has a hydroxyl (OH) group at position 2, whereas deoxyribose sugar has a hydrogen (H)…

Answered: Consider this structure. CH₂OH HO Part…

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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6. b. Draw a box around the disulfide bridge in oxytocin, if present, or write "none". 7. Mark each peptide bond in oxytocin by making the corresponding line in the structure thicker or marking it with a different color. The first one is shown for you as an example (in dark orange). 8. Number the central carbon of each amino acid in oxytocin by pointing a small arrow to it or by circling the corresponding vertex in the image. Numbers 1 and 2 indicate the central carbons of the first and second amino acids of oxytocin, and are shown for you as an example. 9. Fill out the following table, listing amino acids that make up oxytocin in order, from the N terminus to the C terminus, characterizing each amino acid by the properties of its R group (side chains), and briefly indicating the reasoning for the characterization. You may consult amino acid groupings by category in the slides (or the textbook, p.49), but you must explain the reasoning for each in your own words. CO 1 AA# Abbre- Full…
Explain these diagrams
The structure below shows that of a trisaccharide that is composed of (going from top left to bottom right) galactose, glucose, and fructose. More specifically, the component monosaccharides are [D-galactose, L-galactose], [D-glucose, L-glucose], and [D-fructose, L-fructose] .
Consider this monosaccharide. H H OH H .OH HO H HO H CH₂OH Part: 0/3 Part 1 of 3 Label the chirality center(s) for the monosaccharide by highlighting the carbon(s) in the structure below. H H -OH H -OH HO -H HO -H CH₂OH હે
Consider this structure. Part 1 of 3 но Identify the monosaccharide. Select the single best answer. D-ribose D-2-deoxyribose Part 2 of 3 Identify the base. Select the single best answer. thymine guanine cytosine adenine uracil Part: 2/3 Part 3 of 3 Name the structure. NH₂
Briefly and in simple terms, describe the glycoside bond connecting two monosaccharides in a di- or polysaccharide.
Consider the disaccharide maltose. сон H -= H OH OH Part 1 of 2 д- CH₂OH H H H он Н Н д- ОН Н Он Н Он Classify the glycosidic linkage as a or ẞ. Select the single best answer. α В Part: 1/2 Part 2 of 2 Modify the structure of maltose to show the monosaccharide products that form from hydrolysis. You may draw the structures in any arrangement th you like, so long as they aren't touching. Н он Снон Н -= Он Н снон Н H H Он Н д- Н он -= Н Он H Он
1. (a) The diagram below shows a structure of monosaccharide. CH,OH C=0 H-C-OH НО—С—Н ČH,OH i. Draw the figure above on your answer sheet and indicate ALL chiral carbon(s) in your figure with *. ii. With reference to the number of carbon, the type of carbonyl group and D/L configuration, suggest a name consisting these three properties to describe the monosaccharide shown above. Explain why this monosaccharide is in D- or L- configuration as you suggested in (ii). 111. (b) The diagram below shows different configurations of glucose. CH,OH CHO ÇH,OH H H-C-OH O. OH H. H. OH H. H OH HO-C-H но H-C-OH но H. H-C-OH OH OH ČH,OH A В C i. Which glucose molecule, A or C, is in a configuration? Explain. ii. What is the name of the conversion among different configurations? iii. Glycosaminoglycans (GAG) consist of modified sugars. Give a name of the typical modification to the sugar. What makes GAG ideal for the fluid in the joints? to
Consider the disaccharide trehalulose. CH₂OH H Н Он H он Н он H CH2 HO Н Н носн,он Он Н Part: 0/3 Part 1 of 3 Highlight the glycosidic linkage in the structure of trehalulose. Снон Н H он Н он Н Он Н CH2 но Н H HỌ/CH,OH Он H ✓
Consider the following cyclic monosaccharide. CH₂OH H H H H OH HO OH Part 1 of 2 OH H Classify the monosaccharide as an aor ẞ isomer. Select the single best answer. ○ẞ isomer a isomer Part: 1/2 Part 2 of 2 Draw the other isomer of the cyclic form using a Haworth projection. Click and drag to start drawing a structure. ם' G
Consider the structure shown below. он 3 5 CH; O CH, O H CH; O 1 H-N-CH,-C-N-CH;-C-N-CH-C-N-CH-C-N-CH-C-ơ 2 H. H H Fill in the blank with an integer (1, 2, 3, 4, 5..) as shown in the diagram or to represent a specified number. A hydrophilic side chain is indicated by the number
Hhhh

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Consider this structure. CH₂OH HO Part 1 of 3 NH Identify the monosaccharide. Select the single best answer. D-2-deoxyribose D-ribose Part 2 of 3 Identify the base. Select the single best answer. thymine guanine cytosine adenine Ouracil Part: 2/3 Part 3 of 3 Name the structure. х NH₂