3n2p: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:3n2p.jpg|left|200px]] | |||
The | <!-- | ||
The line below this paragraph, containing "STRUCTURE_3n2p", 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_3n2p| PDB=3n2p | SCENE= }} | |||
===Crystal structure of humban carbonic anhydrase 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== | |||
[[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]. | |||
==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 09:22, 9 March 2011
Crystal structure of humban carbonic anhydrase II in complex with a benzenesulfonamide inhibitorCrystal structure of humban carbonic anhydrase II in complex with a benzenesulfonamide inhibitor
Template:ABSTRACT PUBMED 20922253
About this StructureAbout this Structure
3n2p is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
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