3n3j

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[[Image:3n3j.jpg|left|200px]]
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{{STRUCTURE_3n3j| PDB=3n3j | SCENE= }}
{{STRUCTURE_3n3j| PDB=3n3j | SCENE= }}
===Crystal structure of human 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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{{ABSTRACT_PUBMED_20922253}}
{{ABSTRACT_PUBMED_20922253}}
==About this Structure==
==About this Structure==
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[[3n3j]] 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=3N3J OCA].
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[[3n3j]] 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=3N3J OCA].
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==See Also==
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*[[Carbonic anhydrase|Carbonic anhydrase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:20922253</ref><references group="xtra"/>
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<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.]]
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[[Category: Benzenesulfonamide]]
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[[Category: Glycerol]]
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[[Category: Inhibitor]]
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[[Category: Lyase]]
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[[Category: Lyase-lyase inhibitor complex]]
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[[Category: Metalloenzyme]]
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[[Category: Zinc ligand]]

Revision as of 06:49, 26 July 2012

Template:STRUCTURE 3n3j

Contents

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

Template:ABSTRACT PUBMED 20922253

About this Structure

3n3j is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • 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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