3mzc
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | + | [[Image:3mzc.jpg|left|200px]] | |
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3mzc", creates the "Structure Box" on the page. | ||
| + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| + | or leave the SCENE parameter empty for the default display. | ||
| + | --> | ||
| + | {{STRUCTURE_3mzc| PDB=3mzc | SCENE= }} | ||
| - | + | ===Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor=== | |
| - | Description: Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor | ||
| - | + | <!-- | |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_20922253}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 20922253 is the PubMed ID number. | ||
| + | --> | ||
| + | {{ABSTRACT_PUBMED_20922253}} | ||
| + | |||
| + | ==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]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:20922253</ref><references group="xtra"/> | ||
| + | [[Category: Carbonate dehydratase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Avvaru, B S.]] | ||
| + | [[Category: Mckenna, R.]] | ||
| + | [[Category: Robbins, A H.]] | ||
| + | [[Category: Wagner, J.]] | ||
Revision as of 06:21, 9 March 2011
Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor
Template:ABSTRACT PUBMED 20922253
About this Structure
3mzc is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
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
