1cra: Difference between revisions

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New page: left|200px<br /> <applet load="1cra" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cra, resolution 1.9Å" /> '''THE COMPLEX BETWEEN ...
 
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[[Image:1cra.gif|left|200px]]<br />
[[Image:1cra.gif|left|200px]]<br /><applet load="1cra" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1cra" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1cra, resolution 1.9&Aring;" />
caption="1cra, resolution 1.9&Aring;" />
'''THE COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND THE AROMATIC INHIBITOR 1,2,4-TRIAZOLE'''<br />
'''THE COMPLEX BETWEEN HUMAN CARBONIC ANHYDRASE II AND THE AROMATIC INHIBITOR 1,2,4-TRIAZOLE'''<br />


==Overview==
==Overview==
The X-ray crystal structure of the complex between human carbonic, anhydrase II and the inhibitor 1,2,4-triazole has been refined at 1.9 A, resolution to a final R-factor of 0.153. Triazole is an analogue of the, competitive inhibitor imidazole, but the crystal structure shows a, different type of binding to the enzyme. 1,2,4-Triazole is directly bound, to the zinc(II) ion through the nitrogen in position 4, replacing the, native water/hydroxyl (Wat263) in a distorted four-co-ordinated complex., The interaction of the inhibitor with the active site is completed by two, hydrogen bonds to O gamma of Thr200 and to the amide nitrogen atom of, Thr199 through the two adjacent N-1 and N-2 atoms. The binding site of, triazole overlaps the proposed binding sites for the substrates, explaining the observed competitive behaviour of the inhibitor towards, CO2/HCO3- under equilibrium conditions.
The X-ray crystal structure of the complex between human carbonic anhydrase II and the inhibitor 1,2,4-triazole has been refined at 1.9 A resolution to a final R-factor of 0.153. Triazole is an analogue of the competitive inhibitor imidazole, but the crystal structure shows a different type of binding to the enzyme. 1,2,4-Triazole is directly bound to the zinc(II) ion through the nitrogen in position 4, replacing the native water/hydroxyl (Wat263) in a distorted four-co-ordinated complex. The interaction of the inhibitor with the active site is completed by two hydrogen bonds to O gamma of Thr200 and to the amide nitrogen atom of Thr199 through the two adjacent N-1 and N-2 atoms. The binding site of triazole overlaps the proposed binding sites for the substrates, explaining the observed competitive behaviour of the inhibitor towards CO2/HCO3- under equilibrium conditions.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1CRA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ZN, HG, ACE and TRI as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CRA OCA].  
1CRA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=HG:'>HG</scene>, <scene name='pdbligand=ACE:'>ACE</scene> and <scene name='pdbligand=TRI:'>TRI</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CRA OCA].  


==Reference==
==Reference==
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[[Category: lyase(oxo-acid)]]
[[Category: lyase(oxo-acid)]]


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