3n2p: Difference between revisions
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[[Image:3n2p. | [[Image:3n2p.png|left|200px]] | ||
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{{STRUCTURE_3n2p| PDB=3n2p | SCENE= }} | {{STRUCTURE_3n2p| PDB=3n2p | SCENE= }} | ||
===Crystal structure of | ===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: | <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 08:19, 7 September 2011
Crystal structure of human carbonic anhydrase II in complex with a benzenesulfonamide inhibitorCrystal structure of human carbonic anhydrase II in complex with a benzenesulfonamide inhibitor
Template:ABSTRACT PUBMED 20922253
About this StructureAbout this Structure
3n2p is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ 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