3r16
From Proteopedia
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| - | [[Image:3r16. | + | [[Image:3r16.png|left|200px]] |
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===Human CAII bound to N-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide=== | ===Human CAII bound to N-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide=== | ||
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_21620713}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 21620713 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_21620713}} | ||
==About this Structure== | ==About this Structure== | ||
| - | [[3r16]] 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=3R16 OCA]. | + | [[3r16]] 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=3R16 OCA]. |
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| + | ==See Also== | ||
| + | *[[Carbonic anhydrase]] | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:021620713</ref><references group="xtra"/> | ||
[[Category: Carbonate dehydratase]] | [[Category: Carbonate dehydratase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: McKenna, R.]] | [[Category: McKenna, R.]] | ||
[[Category: Supuran, C T.]] | [[Category: Supuran, C T.]] | ||
| + | [[Category: Lyase]] | ||
| + | [[Category: Reversible hydration of carbondioxide]] | ||
Revision as of 05:26, 15 June 2011
Contents |
Human CAII bound to N-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
Template:ABSTRACT PUBMED 21620713
About this Structure
3r16 is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Biswas S, Aggarwal M, Guzel O, Scozzafava A, McKenna R, Supuran CT. Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms. Bioorg Med Chem. 2011 Jun 15;19(12):3732-8. Epub 2011 May 10. PMID:21620713 doi:10.1016/j.bmc.2011.05.006
