Sandbox 156: Difference between revisions

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=== Reaction of CAT III ===
=== Reaction of CAT III ===
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Both reactions take place in the binding site of chloramphenicol, where acetyl-CoA is tunneled through from the opposing side of the trimer<ref>PMID: 3288984</ref>.
Both reactions take place in the active site of CAT III, where acetyl-CoA is tunneled through from the opposing side of the trimer<ref>PMID: 3288984</ref>.


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[[Image:Picture2.jpg|500x400 px|center]]
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===The Active Site===
===The Active Site===


The active site, also the chloramphenicol binding site, catalyzes sequential acetylations of the chloramphenicol molecule. This is initiated by the deprotonation of the 3-hydroxyl of chloramphenicol by <scene name='Sandbox_156/Scene_two/1'>His-195</scene><ref>PMID:2015231</ref>. Numerous hydrogen bonds are present and, importantly, van der Waals interactions between the benzene ring of the <scene name='Sandbox_156/Scene_4/1'>Tyr-25</scene> residue and the imidazole ring. This van der Waals contact may help stabilize side-chain orientations, promoting specificity in the reaction. The acetyl group is already properly positioned after tunneling, and reacts readily without any major structural changes<ref>PMID: 3288984</ref>.  
The active site catalyzes sequential acetylations of the chloramphenicol molecule. This is initiated by the deprotonation of the 3-hydroxyl of chloramphenicol by <scene name='Sandbox_156/Scene_two/1'>His-195</scene><ref>PMID:2015231</ref>. Numerous hydrogen bonds are present and, importantly, van der Waals interactions between the benzene ring of the <scene name='Sandbox_156/Scene_4/1'>Tyr-25</scene> residue and the imidazole ring. This van der Waals contact may help stabilize side-chain orientations, promoting specificity in the reaction. The acetyl group is already properly positioned after tunneling, and reacts readily without any major structural changes<ref>PMID: 3288984</ref>.  
Ace-coa.gif
Ace-coa.gif