**Title: Understanding the Conversion from α-D-glucose-6-phosphate to myo-inositol-1-phosphate**### Chemical Reaction ExplanationIn the image, a chemical reaction facilitated by the enzyme *myo-inositol-1-phosphate synthase* is depicted. This reaction converts α-D-glucose-6-phosphate to myo-inositol-1-phosphate.#### Chemical Structures:- **α-D-glucose-6-phosphate**: - A hexose sugar with a phosphate group at the 6-position. The structure shows the sugar ring with hydroxyl groups (OH) and one phosphate group (O₃PO²⁻) attached.- **myo-inositol-1-phosphate**: - A cyclohexane structure with multiple hydroxyl groups (OH) and a phosphate group (O₃PO²⁻) at the 1-position. The reaction is reversible, as indicated by the two-way arrow, showing the interconversion between these molecules.### Student Exercisesa. **Determine Configuration**: Identify the absolute configuration (R or S) at C-2 of naturally occurring α-D-glucose-6-phosphate.b. **Draw Enantiomer**: Using unambiguous notation, draw the enantiomer (mirror image) of myo-inositol-1-phosphate. Place your drawing in the provided space.

Answered: Image /qna-images/answer/b7294d6f-e68c-4a84-a5a1-9fa3202d5055.jpg

OPO 2- 2-03PO HO myo-inositol-1-phosphate synthase HO HO HO HO" "OH (1) ÕH a-D-glucose-6-phosphate myo-inositol-1-phosphate a. What is the absolute configuration (R or S) at C-2 of naturally occurring a-D-glucose-6-phosphate? p. Using any unambiguous notation, draw the enantiomer (mirror image) of myo- inositol-1-phosphate. Place your answer in the space provided here.

OPO 2- 2-03PO HO myo-inositol-1-phosphate synthase HO HO HO HO" "OH (1) ÕH a-D-glucose-6-phosphate myo-inositol-1-phosphate a. What is the absolute configuration (R or S) at C-2 of naturally occurring a-D-glucose-6-phosphate? p. Using any unambiguous notation, draw the enantiomer (mirror image) of myo- inositol-1-phosphate. Place your answer in the space provided here.

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...

See similar textbooks

Similar questions

Choose the enzyme and cofactors involved in the reaction of oxaloacetate to phosphoenolpyruvate in gluconeogenesis. all K 00 OPO 200 00 C D E glyceraldehyde-3-phosphate dehydrogenase phosphoglycerate kinase pyruvate carboxylase phosphoenolpyruvate carboxykinase Done phosphoglycerate mutase
ACTIVITY-4. Refer to the structures below. Draw the Haworth formula (pyranose) -OH но H- FOH FOH- но но H- H FOH H FOH- H- CH2OH CH2OH Alpha-D- glucopyranose Beta-D-glucopyranose (Haworth) Beta-D-glucopyranose Alpha-D- glucopyranose (Haworth) ACTIVITY-5. Draw the Haworth formula for D-mannose and D-galactose. Label the alpha and beta anomer. CYCLIC FORMS OF FRUCTOSE D-fructose, a ketohexose sugar, can be presented using furanose and pyranose. Cyclic Fisher (furanose) 1 2OH Open chain Fisher Haworth formula (furanose) 1 CH2OH HOH,C- 1 2 F0 НО 3_H. ÇH2OH ÇH2OH но з—н 4 H- H но 2 H-4 HO- H- 5. OH 13 H-5 FOH 6 CH,OH 14 OH H. 6 CH2OH D-fructose Alpha form Alpha form Cyclic Fisher (pyranose) Haworth formula (pyranose) 1 HOH2C-2 3. 1 HO- CH2OH Но H. 5 он 2 H-4 HO- Но 4 OH 3 H-5 FHO- OH H-6 H Alpha form of D-fructose Alpha form of D-fructose ACTIVITY-6. Draw the Fisher and Haworth formula for beta-D-fructose (furanose and pyranose form). Label the beta furanose and beta pyranose.
Identify each given example as describing either a glycolysis intermediate or another compound. Glycolysis intermediate Other compound fructose COO™ c-o- -POS || CH₂ HO CH₂ OH OH Answer Bank a five-carbon phosphorylated compound H-C=O H-C-OH H-C-O-PO H -²0₂PO. CH₂ OH H₂C-OPO OH 2-
エエO 6. Draw the beta-Haworth projection for the following carbohydrate. ( HO HO HO HO H. OH HO HO H- H- HO- HO- H- -HO- alomaxe ns yionsbi bns sla nsT ageinil ( ) OH les
Please answer 4,5,6
For the sugar below OH CH2OH OH OH O-glycosidic bond in the beta configuration N-glycosidic bond in the beta configuration O-glycosidic bond in the alpha configuration it does not have a glycosidic bond O N-glycosidic bond in the alpha configuration OH Draw this with a phosphate group attached to the 4 position: Choose File No file chosen This contains a(n)
1. Identify the most likely additional substrates, products, and coen- zymes for each reaction in the following imaginary pathway. COO Н—с—NH— сно CoO COO CH, Н—с—NH—сно H-C-NH3 CH2 CH2 CH2 CH2 H-C-CH3 H-C-CH3 H-C-NH, H-C-NH3 H-C-NH3 COO COO || C-NH2 || C-NH2 C- NH2 H-C-NH3 H-C-NH3 H-C-NH-CH3 CH2 CH2 CH2 H-C-CH3 H-C-CH3 H-C-CH3 H-C- NH3 C=0 C=0 CoO CoO COO -0- O=0- -
None
2. Using arrow formalism, draw the reaction mechanism for the steps of glycolysis specified below. a. hexokinase: glucose B glucose 6P b. phosphoglucoisomerase: glucose 6P + fructose 6P c. aldolase: fructose 1,6 diphosphate B dihydroxyacetone phosphate + glyceraldehyde 3 phosphate d. triosephosphate isomerase: DHAP + GAP
In the 1st reaction of citric acid cycle, acetyl CoA and oxaloacetate are combined to form citrate as shown below. What is the best way to describe this reaction? CH acetyl Col CH₂ co exaloncertate HO citrate synthase ço, CH₂ HO-C-00 CH₂ co₂ citrate O It begins with an Aldol reaction followed by hydrolysis of CoA thioester). It begins with a keto-enol tautomerization followed by an Aldol reaction. It involves a Claisen condentation. OIt involves an Aldol condensation. None of the above
91. Subject :- Chemistry
Shortly after adding 14C-labeled glyceraldehyde-3-phosphate to a yeast extract, fructose-1,6-bisphosphate labeled at C-3 and C-4 can be isolated. Where was the 14C-label in glyceraldehyde-3-phosphate?