3caj

From Proteopedia

(Difference between revisions)
Jump to: navigation, search

OCA (Talk | contribs)
(New page: 200px <!-- The line below this paragraph, containing "STRUCTURE_3caj", creates the "Structure Box" on the page. You may change the PDB parameter (which sets the PD...)
Next diff →

Revision as of 11:26, 9 April 2008

Template:STRUCTURE 3caj

Crystal structure of the human carbonic anhydrase II in complex with ethoxzolamide


Overview

Ethoxzolamide, an almost forgotten inhibitor of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), is the only classical inhibitor whose structure in adduct with any isoform was not reported yet. We report here the inhibition data of this molecule with the 12 catalytically active mammalian isozymes (CA I-CA XIV) and the X-ray crystal structure with the cytosolic, ubiquitous isoform CA II. These data are presumably useful for the design of novel CA inhibitors, targeting various CA isozymes, considering that ethoxzolamide was already the lead molecule to obtain the second generation inhibitors, dorzolamide and brinzolamide, clinically used antiglaucoma agents with topical action, as well as various other investigational agents.

About this Structure

3CAJ is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Carbonic anhydrase inhibitors: The X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitors., Di Fiore A, Pedone C, Antel J, Waldeck H, Witte A, Wurl M, Scozzafava A, Supuran CT, De Simone G, Bioorg Med Chem Lett. 2008 Mar 18;. PMID:18359629

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools