3n2p: Difference between revisions

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[[Image:3n2p.jpg|left|200px]]
[[Image:3n2p.png|left|200px]]


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{{STRUCTURE_3n2p|  PDB=3n2p  |  SCENE=  }}  
{{STRUCTURE_3n2p|  PDB=3n2p  |  SCENE=  }}  


===Crystal structure of humban carbonic anhydrase II in complex with a benzenesulfonamide inhibitor===
===Crystal structure of human carbonic anhydrase II in complex with a benzenesulfonamide inhibitor===




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==About this Structure==
==About this Structure==
[[3n2p]] 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=3N2P OCA].  
[[3n2p]] 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=3N2P OCA].  
 
==See Also==
*[[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]]
[[Category: Inhibitor.]]
[[Category: Lyase]]
[[Category: Lyase-lyase inhibitor complex]]
[[Category: Zinc ligand]]
[[Category: Zinc metalloenzyme]]

Revision as of 05:19, 7 September 2011

File:3n2p.png

Template:STRUCTURE 3n2p

Crystal structure of human carbonic anhydrase II in complex with a benzenesulfonamide inhibitor

Template:ABSTRACT PUBMED 20922253

About this Structure

3n2p 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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