1t5g: Difference between revisions

New page: left|200px<br /><applet load="1t5g" size="450" color="white" frame="true" align="right" spinBox="true" caption="1t5g, resolution 2.40Å" /> '''Arginase-F2-L-Argini...
 
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[[Image:1t5g.gif|left|200px]]<br /><applet load="1t5g" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1t5g.gif|left|200px]]<br /><applet load="1t5g" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1t5g, resolution 2.40&Aring;" />
caption="1t5g, resolution 2.40&Aring;" />
'''Arginase-F2-L-Arginine complex'''<br />
'''Arginase-F2-L-Arginine complex'''<br />


==Overview==
==Overview==
Arginase is a manganese metalloenzyme that catalyzes the hydrolysis of, L-arginine to form L-ornithine and urea. The structure and stability of, the binuclear manganese cluster are critical for catalytic activity as it, activates the catalytic nucleophile, metal-bridging hydroxide ion, and, stabilizes the tetrahedral intermediate and its flanking states. Here, we, report X-ray structures of a series of inhibitors bound to the active site, of arginase, and each inhibitor exploits a different mode of coordination, with the Mn(2+)(2) cluster. Specifically, we have studied the binding of, fluoride ion (F(-); an uncompetitive inhibitor) and L-arginine, L-valine, dinor-N(omega)-hydroxy-L-arginine, descarboxy-nor-N(omega)-hydroxy-L-arginine, and, dehydro-2(S)-amino-6-boronohexanoic acid. Some inhibitors, such as, fluoride ion, dinor-N(omega)-hydroxy-L-arginine, and, dehydro-2(S)-amino-6-boronohexanoic acid, cause the net addition of one, ligand to the Mn(2+)(2) cluster. Other inhibitors, such as, descarboxy-nor-N(omega)-hydroxy-L-arginine, simply displace the, metal-bridging hydroxide ion of the native enzyme and do not cause any net, change in the metal coordination polyhedra. The highest affinity, inhibitors displace the metal-bridging hydroxide ion (and sometimes occupy, a Mn(2+)(A) site found vacant in the native enzyme) and maintain a, conserved array of hydrogen bonds with their alpha-amino and -carboxylate, groups.
Arginase is a manganese metalloenzyme that catalyzes the hydrolysis of L-arginine to form L-ornithine and urea. The structure and stability of the binuclear manganese cluster are critical for catalytic activity as it activates the catalytic nucleophile, metal-bridging hydroxide ion, and stabilizes the tetrahedral intermediate and its flanking states. Here, we report X-ray structures of a series of inhibitors bound to the active site of arginase, and each inhibitor exploits a different mode of coordination with the Mn(2+)(2) cluster. Specifically, we have studied the binding of fluoride ion (F(-); an uncompetitive inhibitor) and L-arginine, L-valine, dinor-N(omega)-hydroxy-L-arginine, descarboxy-nor-N(omega)-hydroxy-L-arginine, and dehydro-2(S)-amino-6-boronohexanoic acid. Some inhibitors, such as fluoride ion, dinor-N(omega)-hydroxy-L-arginine, and dehydro-2(S)-amino-6-boronohexanoic acid, cause the net addition of one ligand to the Mn(2+)(2) cluster. Other inhibitors, such as descarboxy-nor-N(omega)-hydroxy-L-arginine, simply displace the metal-bridging hydroxide ion of the native enzyme and do not cause any net change in the metal coordination polyhedra. The highest affinity inhibitors displace the metal-bridging hydroxide ion (and sometimes occupy a Mn(2+)(A) site found vacant in the native enzyme) and maintain a conserved array of hydrogen bonds with their alpha-amino and -carboxylate groups.


==About this Structure==
==About this Structure==
1T5G is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with F, MN and ARG as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Arginase Arginase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.3.1 3.5.3.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1T5G OCA].  
1T5G is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=F:'>F</scene>, <scene name='pdbligand=MN:'>MN</scene> and <scene name='pdbligand=ARG:'>ARG</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Arginase Arginase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.3.1 3.5.3.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1T5G OCA].  


==Reference==
==Reference==
Line 14: Line 14:
[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ash, D.E.]]
[[Category: Ash, D E.]]
[[Category: Boucher, J.L.]]
[[Category: Boucher, J L.]]
[[Category: Cama, E.]]
[[Category: Cama, E.]]
[[Category: Christianson, D.W.]]
[[Category: Christianson, D W.]]
[[Category: Emig, F.A.]]
[[Category: Emig, F A.]]
[[Category: Han, S.]]
[[Category: Han, S.]]
[[Category: Mansuy, D.]]
[[Category: Mansuy, D.]]
[[Category: Pethe, S.]]
[[Category: Pethe, S.]]
[[Category: Viola, R.E.]]
[[Category: Viola, R E.]]
[[Category: ARG]]
[[Category: ARG]]
[[Category: F]]
[[Category: F]]
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[[Category: l-arginine]]
[[Category: l-arginine]]


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