3ml2: Difference between revisions
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[[Image:3ml2. | [[Image:3ml2.png|left|200px]] | ||
{{STRUCTURE_3ml2| PDB=3ml2 | SCENE= }} | {{STRUCTURE_3ml2| PDB=3ml2 | SCENE= }} | ||
===Human carbonic anhydsase II in complex with an aryl sulfonamide inhibitor=== | ===Human carbonic anhydsase II in complex with an aryl sulfonamide inhibitor=== | ||
{{ABSTRACT_PUBMED_20598552}} | {{ABSTRACT_PUBMED_20598552}} | ||
==About this Structure== | ==About this Structure== | ||
[[3ml2]] 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=3ML2 OCA]. | [[3ml2]] 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=3ML2 OCA]. | ||
==See Also== | |||
*[[Carbonic anhydrase|Carbonic anhydrase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:020598552</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: Inhibitor]] | |||
[[Category: Lyase]] | |||
[[Category: Lyase-lyase inhibitor complex]] | |||
[[Category: Metal-binding]] | |||
[[Category: Sulfonamide]] | |||
[[Category: Zinc ligand]] | |||
[[Category: Zinc metalloenzyme]] | |||
Revision as of 00:35, 27 July 2012
Human carbonic anhydsase II in complex with an aryl sulfonamide inhibitor
Template:ABSTRACT PUBMED 20598552
About this Structure
3ml2 is a 1 chain structure of Carbonic anhydrase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Wagner J, Avvaru BS, Robbins AH, Scozzafava A, Supuran CT, McKenna R. Coumarinyl-substituted sulfonamides strongly inhibit several human carbonic anhydrase isoforms: solution and crystallographic investigations. Bioorg Med Chem. 2010 Jul 15;18(14):4873-8. Epub 2010 Jun 15. PMID:20598552 doi:10.1016/j.bmc.2010.06.028