Drag the terms on the left to the appropriate blanks on the right to complete the sentences. Terms can be used once, more than once, or not at all.SubmitdCTPGMPAMPGTPdTTPactivationinhibitiondGTPMy Answers Give UpUTP + Gln + ATP → CTP + Glu+ ADP + P₁. Cofactor:dCMP + H₂O →→→→DUMP + NH3. Cofactor:CDP+ [2H] → dCDP+ H₂O. Cofactor:Effect:Effect:Effect:Reset Help

Nucleotide metabolism is the set of biochemical reactions that involve the synthesis and breakdown…

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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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3. (а) 0.0050 M operate at one-quarter of its maximum rate? At what substrate concentration would an enzyme with a kcat of 30.0 s-1 and a Km of (b) trations [So]: ½ Km, 2 KM, and 10 KM. Determine the fraction of Vmax that would be obtained at the following substrate concen- (c) 1 (HIV-1) has been the object of innumerable studies to develop effective chemotherapeutic agents. It has been shown that p6* known as the late assembly protein is an inhibitor of HIV protease. An assay was developed using an artificial polypeptide substrate containing a p-nitrophenylalanine residue at the cleavage point that undergoes a small change in absorption at 295 nm upon bond hydrolysis that could be followed spectrophotometrically. The cleavage of the peptide bond is shown schematically on the right. Results of the assay are given in the table below. The protease of the human immunodeficiency virus- Lys NH2 Ala Nle Arg Ala Val-Nle-NH-CH-Ċ–NH-Glu CH2 Lys NH2 Ala NO2 Nle Arg H2Ó N HIV-1 protease Ala Vo…
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The purified OXA-M290 enzyme can now be tested to determine which β-lactamase inhibitor is most effective. This inhibitor could be prescribed in combination with a β-lactam antibiotic to treat the infection caused by the E. coli KGH1 strain. Before testing inhibitors against OXA-M290, the kinetic activity of this enzyme must first be measured. The activity of OXA-M290 is measured using nitrocefin, a chromogenic β-lactam antibiotic. When nitrocefin is hydrolyzed by a β-lactamase, it changes from yellow to red in colour. The nitrocefin hydrolysis product has an extinction coefficient of 20,500 M-1 cm-1 at 486 nm. The hydrolysis of 60 μM nitrocefin by 1 nM OXA-M290 is monitored using a microplate reader. The absorbance of the wells in the plate is measured at 486 nm every 30 seconds. This experiment is carried out with three replicates, generating the following data: Time (min) Absorbance of Replicate 1 Absorbance of Replicate 2 Absorbance of Replicate 3 0.5 0.0984…
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