2o4z: Difference between revisions

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[[Image:2o4z.gif|left|200px]]
[[Image:2o4z.gif|left|200px]]


{{Structure
<!--
|PDB= 2o4z |SIZE=350|CAPTION= <scene name='initialview01'>2o4z</scene>, resolution 2.10&Aring;
The line below this paragraph, containing "STRUCTURE_2o4z", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=HG:MERCURY+(II)+ION'>HG</scene>, <scene name='pdbligand=HSW:N-HYDROXYSULFAMIDE'>HSW</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Carbonate_dehydratase Carbonate dehydratase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.2.1.1 4.2.1.1] </span>
or leave the SCENE parameter empty for the default display.
|GENE=  
-->
|DOMAIN=
{{STRUCTURE_2o4z| PDB=2o4z  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2o4z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2o4z OCA], [http://www.ebi.ac.uk/pdbsum/2o4z PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2o4z RCSB]</span>
}}


'''Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor'''
'''Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor'''
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[[Category: Temperini, C.]]
[[Category: Temperini, C.]]
[[Category: Winum, J Y.]]
[[Category: Winum, J Y.]]
[[Category: carbonic anhydrase]]
[[Category: Carbonic anhydrase]]
[[Category: crystal structure]]
[[Category: Crystal structure]]
[[Category: inhibitor]]
[[Category: Inhibitor]]
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 04:12:45 2008''

Revision as of 10:19, 4 May 2008

File:2o4z.gif

Template:STRUCTURE 2o4z

Crystal structure of the Carbonic Anhydrase II complexed with hydroxysulfamide inhibitor


OverviewOverview

N-Hydroxysulfamide is a 2000-fold more potent inhibitor of the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1) as compared to sulfamide. It also inhibits other physiologically relevant isoforms, such as the tumor-associated CA IX and XII (K(I)s in the range of 0.865-1.34microM). In order to understand the binding of this inhibitor to the enzyme active site, the X-ray crystal structure of the human hCA II-N-hydroxysulfamide adduct was resolved. The inhibitor coordinates to the active site zinc ion by the ionized primary amino group, participating in an extended network of hydrogen bonds with amino acid residues Thr199, Thr200 and two water molecules. The additional two hydrogen bonds in which N-hydroxysulfamide bound to hCA II is involved as compared to the corresponding adduct of sulfamide may explain its higher affinity for the enzyme, also providing hints for the design of tight-binding CA inhibitors possessing an organic moiety substituting the NH group in the N-hydroxysulfamide structure.

About this StructureAbout this Structure

2O4Z is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors., Temperini C, Winum JY, Montero JL, Scozzafava A, Supuran CT, Bioorg Med Chem Lett. 2007 May 15;17(10):2795-801. Epub 2007 Feb 28. PMID:17346964 Page seeded by OCA on Sun May 4 10:19:57 2008

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