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3mzc
From Proteopedia
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| - | [[Image:3mzc. | + | [[Image:3mzc.png|left|200px]] |
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{{STRUCTURE_3mzc| PDB=3mzc | SCENE= }} | {{STRUCTURE_3mzc| PDB=3mzc | SCENE= }} | ||
===Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor=== | ===Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor=== | ||
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{{ABSTRACT_PUBMED_20922253}} | {{ABSTRACT_PUBMED_20922253}} | ||
==About this Structure== | ==About this Structure== | ||
| - | [[3mzc]] 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=3MZC OCA]. | + | [[3mzc]] 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=3MZC OCA]. |
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| + | ==See Also== | ||
| + | *[[Carbonic anhydrase|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 inhibitor]] | ||
| + | [[Category: Lyase]] | ||
| + | [[Category: Lyase-lyase inhibitor complex]] | ||
| + | [[Category: Zinc coordination]] | ||
| + | [[Category: Zinc metalloenzyme]] | ||
Revision as of 21:07, 26 July 2012
Contents |
Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor
Template:ABSTRACT PUBMED 20922253
About this Structure
3mzc 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
