2ima: Difference between revisions

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[[Image:2ima.jpg|left|200px]]
{{Seed}}
[[Image:2ima.png|left|200px]]


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{{STRUCTURE_2ima|  PDB=2ima  |  SCENE=  }}  
{{STRUCTURE_2ima|  PDB=2ima  |  SCENE=  }}  


'''Clostridium botulinum Neurotoxin Serotype A Light Chain Inhibited by 2,4-dichlorocinnamic hydroxamate'''
===Clostridium botulinum Neurotoxin Serotype A Light Chain Inhibited by 2,4-dichlorocinnamic hydroxamate===




==Overview==
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The potential for the use of Clostridial neurotoxins as bioweapons makes the development of small-molecule inhibitors of these deadly toxins a top priority. Recently, screening of a random hydroxamate library identified a small-molecule inhibitor of C. botulinum Neurotoxin Serotype A Light Chain (BoNT/A-LC), 4-chlorocinnamic hydroxamate, a derivative of which has been shown to have in vivo efficacy in mice and no toxicity. We describe the X-ray crystal structures of BoNT/A-LC in complexes with two potent small-molecule inhibitors. The structures of the enzyme with 4-chlorocinnamic hydroxamate or 2,4-dichlorocinnamic hydroxamate bound are compared to the structure of the enzyme complexed with L-arginine hydroxamate, an inhibitor with modest affinity. Taken together, this suite of structures provides surprising insights into the BoNT/A-LC active site, including unexpected conformational flexibility at the S1' site that changes the electrostatic environment of the binding pocket. Information gained from these structures will inform the design and optimization of more effective small-molecule inhibitors of BoNT/A-LC.
The line below this paragraph, {{ABSTRACT_PUBMED_17524984}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_17524984}}


==About this Structure==
==About this Structure==
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[[Category: Substrate specificity]]
[[Category: Substrate specificity]]
[[Category: Substrate switching]]
[[Category: Substrate switching]]
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