part 2 1Using Haworth projections, draw the structure of an a-disaccharide of mannoseB(1,2) galactose (mannose is the C-2 epimer of glucose, galactose is the C-4 epimer of glucose).Using the disaccharide that you have drawn, show one interaction that would occur between C-4of galactose and the R-group of His at pH 7. You will need to draw the structure of His. Use adotted line between the specific atoms to indicate the interaction. What type of interaction is this?O 2022 Arizona State University Online2.Draw the structure of the fatty acid, 16:247,10, as it occurs at pH 7. Make sure doublebonds have the correct configuration. Using the omega numbering system for fatty acids, whattype of fatty acid is this? © 2022 Arizona State University Online3.Draw a diagram that shows the formation of the sodium gradient using ATP coupledto active transport of glucose using the sodium gradient. Clearly label the sides of the membraneand transporter(s) used. Clearly show the direction of ion/molecule movement and the number ofions/molecules moving. O 2022 Arizona State University Online4.1The following curve shows typical hemoglobin to oxygen binding. Draw the curve onyour paper, then draw and clearly label curves for hemoglobin-oxygen binding following (1)decreased CO2 and (2) decreased pH. O 2022 Arizona State University OnlineV30%20100%Degree of saturation6080Og pressure (pOg in torr)40100

Fatty acids can be named and numbered in 2 ways. Fatty acids have a carboxylate end (COO- ) and a…

Answered: 2. Draw the structure of the fatty…

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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. Draw Haworth projections for the following: (a) CHO in a-furanose form. Name the sugar. H-C-OH | HO-C-H H-C-OH CH,OH (b) The L isomer of (a) (c) a-D-GlcNAc (d) a-D-Fructofuranose
Draw Haworth projections formulas for dimers of glucose with the following glycosidic linkages: 1. An alpha (1-4) linkage 2. A beta (1-6) linkage
Using Haworth projections, how can I draw a hetero trisaccharide containing two different types of glycosidic bonds? Also provide the names of each monosaccharide in the chain.
Imagine a trisaccharide that has D-Altrose, D-Gulose, and D-Ribose. D-Altrose is bonded to D-Gulose in an α(1→4) glycosidic bond and D-Ribose is bonded to D-Altrose in an α(1→6) glycosidic bond. Draw the imaginary trisaccharide using Haworth projection with the appropriate representation of each monosaccharide.
Suppose a polymer of glucose with alternating α(1-->4) and β(1-->4) glycosidic linkages has just been discovered. Draw a Haworth projection for a repeating tetramer (ie, two repeating dimers) of such a polysaccharide. Insert a photo of your drawing here. - Would you expect the polymer from Q13 to have primarily a structural role or an energy storage role in an organism? Briefly explain. - What type of organism, if any, might use the polysaccharide from Q13 as a food source?
Carbohydrates Instructions: (A) Show the conversion from Fischer to Haworth projections. (B) Draw and give the systematic names of the two (2) possible Haworth structures for the following monosaccharides. 1. D- Galactose
Carbohydrates Instructions: (A) Show the conversion from Fischer to Haworth projections. (B) Draw and give the systematic names of the two (2) possible Haworth structures for the following monosaccharides. 1.D- Ribose 2. D- Galactose 3. D- Fructose
16-24 diastereomers? Explain your answer. Both? when the motecue hasonly che stereocenter then the epiners are encintomers. When the molecule hastwo umor ster Draw Haworth projection formulas for dimers of glucose having the a B1-4 linkage (both molecules of glucose in the B form) a) b) c) an a,a (1-1) linkage a B1-6 linkage between 2 ß-glucose units epime are dia ster
Suppose a polymer of glucose with alternating α(1-->4) and β(1-->4) glycosidic linkages has just been discovered. Draw a Haworth projection for a repeating tetramer (ie, two repeating dimers) of such a polysaccharide. What organism might use this as a food source?
Ala-Arg-Val-His-Asp-Gln Given the polypeptide chain above Estimate the net charge of the polypeptide chain at physiological pH (7.4) and at pH 5.0 . How many peptide bonds are there? What kind of polypeptide is it?
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1. Draw the structure of the L-isomer of the Fisher projection of one epimer of D-allopyronoside. Discuss why is this an epimer of the monosaccharide. 2. Is this saccharide a good substrate for glycolysis? Explain.

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2. Draw the structure of the fatty acid, 16:247,10, as it occurs at pH 7. Make sure double bonds have the correct configuration. Using the omega numbering system for fatty acids, what type of fatty acid is this? © 2022 Arizona State University Online