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(a) Which antibacterial compound does NOT directly inhibit this process? H₂N NH cycloserine A Ph CO₂H penicillin G B OH NH₂ B-fluoro-L-alanine C H3C NH (b) Which statement about the "Park nucleotide" is correct? A. the N-acetylglucosamine ring is the L-enantiomer B. the diphosphate group at the anomeric center forms exclusively as the ß-anomer C. the five amino acids all have D configurations D. the anomeric center of the glucosamine ring has R configuration

(a) Which antibacterial compound does NOT directly inhibit this process? H₂N NH cycloserine A Ph CO₂H penicillin G B OH NH₂ B-fluoro-L-alanine C H3C NH (b) Which statement about the "Park nucleotide" is correct? A. the N-acetylglucosamine ring is the L-enantiomer B. the diphosphate group at the anomeric center forms exclusively as the ß-anomer C. the five amino acids all have D configurations D. the anomeric center of the glucosamine ring has R configuration

Biochemistry
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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7. To prepare the "Park nucleotide", five amino acids must be attached to the lactide intermediate. HO- HO ACHN O OH 6969 lactide intermediate O. HO ÕH _H construct pentapeptide НО HOO CO₂H H₂C ACHNO. N-H HO₂C Park nucleotide j H (a) Which antibacterial compound does NOT directly inhibit this process? H₂N ad ex NH P o'90'9 OH H NH₂ B-fluoro-L-alanine 0. HO ÕH H NH₂ OH NH₂ OH H H3C cycloserine penicillin G B A (b) Which statement about the "Park nucleotide" is correct? A. the N-acetylglucosamine ring is the L-enantiomer B. the diphosphate group at the anomeric center forms exclusively as the ß-anomer C. the five amino acids all have D configurations D. the anomeric center of the glucosamine ring has R configuration D SCH3 H
Transcribed Image Text:7. To prepare the "Park nucleotide", five amino acids must be attached to the lactide intermediate. HO- HO ACHN O OH 6969 lactide intermediate O. HO ÕH _H construct pentapeptide НО HOO CO₂H H₂C ACHNO. N-H HO₂C Park nucleotide j H (a) Which antibacterial compound does NOT directly inhibit this process? H₂N ad ex NH P o'90'9 OH H NH₂ B-fluoro-L-alanine 0. HO ÕH H NH₂ OH NH₂ OH H H3C cycloserine penicillin G B A (b) Which statement about the "Park nucleotide" is correct? A. the N-acetylglucosamine ring is the L-enantiomer B. the diphosphate group at the anomeric center forms exclusively as the ß-anomer C. the five amino acids all have D configurations D. the anomeric center of the glucosamine ring has R configuration D SCH3 H
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