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=" | [[Image:1t5g.gif|left|200px]]<br /><applet load="1t5g" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1t5g, resolution 2.40Å" /> | caption="1t5g, resolution 2.40Å" /> | ||
'''Arginase-F2-L-Arginine complex'''<br /> | '''Arginase-F2-L-Arginine complex'''<br /> | ||
==Overview== | ==Overview== | ||
Arginase is a manganese metalloenzyme that catalyzes the hydrolysis of | 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:// | 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== | ||
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[[Category: Rattus norvegicus]] | [[Category: Rattus norvegicus]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Ash, D | [[Category: Ash, D E.]] | ||
[[Category: Boucher, J | [[Category: Boucher, J L.]] | ||
[[Category: Cama, E.]] | [[Category: Cama, E.]] | ||
[[Category: Christianson, D | [[Category: Christianson, D W.]] | ||
[[Category: Emig, F | [[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 | [[Category: Viola, R E.]] | ||
[[Category: ARG]] | [[Category: ARG]] | ||
[[Category: F]] | [[Category: F]] | ||
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[[Category: l-arginine]] | [[Category: l-arginine]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:10:06 2008'' |