a) Please draw the products form the following reaction catalyzed by a restriction enzyme includingstereochemistry. Also state whether the stereochemistry at P is inverted or conserved.thymineH₂Hadenine

Answered: Image /qna-images/answer/b72baa53-7ccd-4338-a9c6-735a639e7ec1.jpg

Answered: a) Please draw the products form the…

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter1: Lewis Structures

Section: Chapter Questions

Problem 75EQ

See similar textbooks

Similar questions

Draw a diagram of the linear and ring structures of ribose. Show the biochemical mechanism of cyclization of each and name the resultant ring – including the ring type & anomeric carbon designation. Draw and name an amine version, reduced version, and oxidized version, either in ring or Fisher projection.
Catalytic antibodies catalyze a reaction by forcing the conformation of the substrate in the direction of the transition state. The synthesis of the antibody is carried out in the presence of a transition state analog—a stable molecule that structurally resembles the transition state. This causes an antibody to be generated that recognizes and binds to the transition state, thereby stabilizing it. For example, the following transition state analog has been used to generate a catalytic antibody that catalyzes the hydrolysis of the structurally similar ester: a. Draw a possible transition state for the hydrolysis reaction. b. The following transition state analog is used to generate a catalytic antibody for the catalysis of ester hydrolysis. Draw the structure of an ester whose rate of hydrolysis would be increased by this catalytic antibody.
Draw the complete electron pushing mechanism that is enzyme catalyzed.
1. Aminoacyl-tRNA is used for peptide synthesis. It is synthesized by aminoacyl tRNA synthetase, via an ATP-dependent mechanism. Review what was discussed in lecture about aminoacyl tRNA synthetase and draw a stepwise mechanism for the reaction using arrow formalism. Include any relevant intermediates. You may abbreviate adenosine or adenine as necessary. NH2 tRNA но OH NH2 но он NH tRNA ATP protein synthesis "AMP-aa" "ERNA-aa" O он "H3N- R PPI AMP "H3N CO2 ARS ARS amino acid ARS (aa)
e) 4) Identify the type of glycosidic bond for each of the following sugars. Choose from a-(1→2), a-(1-3), a-(1-4), a-(1-5), a-(1-6), B-(1-2), B-(1-3), B-(1-4), B (15), B-(1-6), or a,ß-(142) a) c) HO b) Н H CH OH а H OH N H ОН Н CH₂OH OH H CI CH₂OH N HO HO H Н ОН HO Н H HO H H CH OH хох OH H H 0 H CH₂OH CH₂ OH H НО CH2OH H HO Н O HO Н HO H 0 H b. HO Н H Н d) CH₂OH НО H - 0 Н H OH НО CH OH H HO Н И H ОН 9 HOCH₂ OH H Н ОН CH₂OH 5 H OH H H Но Н CI H N 5. Determine the number of chiral carbons in the following structures, and how many stereoisomers are possible. НО HO H H CH OH
Find the product of this enzyme catalyzed reaction.
The enzyme that catalyzes the Ca ¬ Cb bond cleavage reaction that converts serine to glycine removes thesubstituent (R) bonded to the a-carbon in the first step of the reaction. Starting with PLP bound to serine inan imine linkage, propose a mechanism for this reaction. (Hint: The first step involves removal of the protonfrom serine’s OH group.)
Which of the following enzymes catalyzes a reaction with the pictured compound as an intermediate? = Hz C—6 ཆོས་རིག་ག་ག་ག་ག་ག་གས་པ་ 0—P, O succinyl-CoA synthetase fumarase succinate dehydrogenase malate dehydrogenase a-ketoglutarate dehydrogenase
The following figure shows the intermediate of the transketolase mechanism. Use arrow pushing to form the resonance stabilized enzyme intermediate. Show the mechanism for reaction of this intermediate with the given aldose, using the protonated acid/base residue suppliec by the enzyme. Clearly show the product of the reaction and make sure that the acid/base residue ends up in the protonated state at the end or your mechanism. H. CH,OH H-B H- HO- OH H- OH CH,OPO,
18.35a1 Draw step 1 of the mechanism. Br Edit + OH
Part B Determine whether each of the following molecules are activators or inhibitors of gluconeogenesis. Drag the appropriate compounds to their respective bins. > View Available Hint(s) Reset Help adenosine diphosphate (ADP) fructose-1,6-bisphosphate (F-1,6-BP) glucose-6-phosphate (G-6-P) adenosine monophosphate (AMP) glucagon insulin acetyl-CoA Activators of gluconeogenesis Inhibitors of gluconeogenesis Neither an activator nor inhibitor of gluconeogenesis Submit
FInd the product of this enzyme catalyzed reaction.

SEE MORE QUESTIONS

Recommended textbooks for you

Pushing Electrons

Chemistry

ISBN:

9781133951889

Author:

Weeks, Daniel P.

Publisher:

Cengage Learning

Introduction to General, Organic and Biochemistry

Chemistry

ISBN:

9781285869759

Author:

Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Pushing Electrons

Chemistry

ISBN:

9781133951889

Author:

Weeks, Daniel P.

Publisher:

Cengage Learning

Introduction to General, Organic and Biochemistry

Chemistry

ISBN:

9781285869759

Author:

Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Chemistry & Chemical Reactivity

Chemistry

ISBN:

9781337399074

Author:

John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

a) Please draw the products form the following reaction catalyzed by a restriction enzyme including stereochemistry. Also state whether the stereochemistry at P is inverted or conserved. thymine H₂ H adenine