Sandbox 156

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<table style="background-color:#ffffc0" cellpadding="8" width="95%" border="0"><tr><td>Please do NOT make changes to this Sandbox until after April 23, 2010. Sandboxes 151-200 are reserved until then for use by the Chemistry 307 class at UNBC taught by Prof. [[User:Andrea Gorrell|Andrea Gorrell]].</td></tr>
 
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Anthony Daniele
 
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= Chloramphenicol Acetyltransferase Type III =
= Chloramphenicol Acetyltransferase Type III =
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==Structure==
==Structure==
<applet load='4CLA' size='300' frame='true' align='right' caption='' />
<applet load='4CLA' size='300' frame='true' align='right' caption='' />
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<table style="background-color:#ffffc0" cellpadding="8" width="95%" border="0"><tr><td>Please do NOT make changes to this Sandbox until after April 23, 2010. Sandboxes 151-200 are reserved until then for use by the Chemistry 307 class at UNBC taught by Prof. [[User:Andrea Gorrell|Andrea Gorrell]].</td></tr>

Revision as of 04:45, 21 March 2010

Contents

Chloramphenicol Acetyltransferase Type III

Chloramphenicol acetyltransferase type III (CAT III) is an enzyme which catalyzes the transfer of an acetyl group from acetyl-CoA to hydroxyl groups of chloramphenicol. CAT III is a trimeric protein

Introduction

Reaction of CAT III



In the first step of the reaction, Histidine-156 abstracts a proton from the 3-hydroxyl of chloramphenicol, promoting a nucleophilic attack from the deprotonated oxygen to the thioester bond of the acetyl-CoA. The intermediate produced, 3-acetylchloramphenicol, then rearranges non-enzymatically to 1-acetylchloramphenicol. Regeneration of the 3-hydroxyl allows another CAT III catalyzed nucleophilic attack to another acetyl-CoA and a 1,3-diacetylchloramphenicol product is formed.

Structure

PDB ID 4CLA

Drag the structure with the mouse to rotate







Please do NOT make changes to this Sandbox until after April 23, 2010. Sandboxes 151-200 are reserved until then for use by the Chemistry 307 class at UNBC taught by Prof. Andrea Gorrell.
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