3mzc: Difference between revisions

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[[Image:3mzc.jpg|left|200px]]
[[Image:3mzc.png|left|200px]]


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{{STRUCTURE_3mzc|  PDB=3mzc  |  SCENE=  }}  
{{STRUCTURE_3mzc|  PDB=3mzc  |  SCENE=  }}  


===Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor===
===Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor===


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{{ABSTRACT_PUBMED_20922253}}
{{ABSTRACT_PUBMED_20922253}}


==About this Structure==
==About this Structure==
[[3mzc]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3MZC OCA].  
[[3mzc]] is a 1 chain structure of [[Carbonic anhydrase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3MZC OCA].  
 
==See Also==
*[[Carbonic anhydrase|Carbonic anhydrase]]


==Reference==
==Reference==
<ref group="xtra">PMID:20922253</ref><references group="xtra"/>
<ref group="xtra">PMID:020922253</ref><references group="xtra"/>
[[Category: Carbonate dehydratase]]
[[Category: Carbonate dehydratase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Robbins, A H.]]
[[Category: Robbins, A H.]]
[[Category: Wagner, J.]]
[[Category: Wagner, J.]]
[[Category: Benzenesulfonamide inhibitor]]
[[Category: Lyase]]
[[Category: Lyase-lyase inhibitor complex]]
[[Category: Zinc coordination]]
[[Category: Zinc metalloenzyme]]

Revision as of 21:07, 26 July 2012

File:3mzc.png

Template:STRUCTURE 3mzc

Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor

Template:ABSTRACT PUBMED 20922253

About this Structure

3mzc is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  1. Pacchiano F, Aggarwal M, Avvaru BS, Robbins AH, Scozzafava A, McKenna R, Supuran CT. Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency. Chem Commun (Camb). 2010 Nov 28;46(44):8371-3. Epub 2010 Oct 5. PMID:20922253 doi:10.1039/c0cc02707c

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