2o4z

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[[Image:2o4z.png|left|200px]]
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{{STRUCTURE_2o4z| PDB=2o4z | SCENE= }}
{{STRUCTURE_2o4z| PDB=2o4z | SCENE= }}
===Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor===
===Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor===
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{{ABSTRACT_PUBMED_17346964}}
{{ABSTRACT_PUBMED_17346964}}
==About this Structure==
==About this Structure==
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2O4Z is a 1 chain structure of 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=2O4Z OCA].
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[[2o4z]] 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=2O4Z 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:17346964</ref><references group="xtra"/>
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<ref group="xtra">PMID:017346964</ref><references group="xtra"/>
[[Category: Carbonate dehydratase]]
[[Category: Carbonate dehydratase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Winum, J Y.]]
[[Category: Winum, J Y.]]
[[Category: Carbonic anhydrase]]
[[Category: Carbonic anhydrase]]
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[[Category: Crystal structure]]
 
[[Category: Inhibitor]]
[[Category: Inhibitor]]
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[[Category: Lyase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 22:08:28 2009''
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Revision as of 01:17, 26 July 2012

Template:STRUCTURE 2o4z

Contents

Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor

Template:ABSTRACT PUBMED 17346964

About this Structure

2o4z is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Temperini C, Winum JY, Montero JL, Scozzafava A, Supuran CT. Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors. Bioorg Med Chem Lett. 2007 May 15;17(10):2795-801. Epub 2007 Feb 28. PMID:17346964 doi:http://dx.doi.org/10.1016/j.bmcl.2007.02.068

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