3ibi
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
| - | + | [[3ibi]] 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=3IBI OCA]. | |
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| + | ==See Also== | ||
| + | *[[Carbonic anhydrase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:019731956</ref><references group="xtra"/> |
[[Category: Carbonate dehydratase]] | [[Category: Carbonate dehydratase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Alterio, V.]] | [[Category: Alterio, V.]] | ||
[[Category: Simone, G De.]] | [[Category: Simone, G De.]] | ||
| - | [[Category: Acetylation]] | ||
[[Category: Aliphatic sulfamate inhibitor]] | [[Category: Aliphatic sulfamate inhibitor]] | ||
[[Category: Carbonic anhydrase ii]] | [[Category: Carbonic anhydrase ii]] | ||
| - | [[Category: Cytoplasm]] | ||
[[Category: Disease mutation]] | [[Category: Disease mutation]] | ||
| - | [[Category: Lyase]] | + | [[Category: Lyase-lyase inhibitor complex]] |
[[Category: Metal-binding]] | [[Category: Metal-binding]] | ||
| - | [[Category: Polymorphism]] | ||
[[Category: Protein-inhibitor complex]] | [[Category: Protein-inhibitor complex]] | ||
| - | [[Category: Zinc]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 23 08:41:34 2009'' | ||
Revision as of 04:55, 24 August 2011
Contents |
The crystal structure of the human carbonic anhydrase II in complex with an aliphatic sulfamate inhibitor
Template:ABSTRACT PUBMED 19731956
About this Structure
3ibi is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Vitale RM, Alterio V, Innocenti A, Winum JY, Monti SM, De Simone G, Supuran CT. Carbonic Anhydrase Inhibitors. Comparison of Aliphatic Sulfamate/Bis-sulfamate Adducts with Isozymes II and IX as a Platform for Designing Tight-Binding, More Isoform-Selective Inhibitors. J Med Chem. 2009 Sep 4. PMID:19731956 doi:10.1021/jm900641r
