1nm0

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(New page: 200px<br /><applet load="1nm0" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nm0, resolution 2.30&Aring;" /> '''Proteus mirabilis ca...)
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[[Image:1nm0.jpg|left|200px]]<br /><applet load="1nm0" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1nm0, resolution 2.30&Aring;" />
caption="1nm0, resolution 2.30&Aring;" />
'''Proteus mirabilis catalase in complex with formiate'''<br />
'''Proteus mirabilis catalase in complex with formiate'''<br />
==Overview==
==Overview==
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The structure of Proteus mirabilis catalase in complex with an inhibitor, formic acid, has been solved at 2.3 A resolution. Formic acid is a key, ligand of catalase because of its ability to react with the ferric enzyme, giving a high-spin iron complex. Alternatively, it can react with two, transient oxidized intermediates of the enzymatic mechanism, compounds I, and II. In this work, the structures of native P. mirabilis catalase (PMC), and compound I have also been determined at high resolution (2.0 and 2.5, A, respectively) from frozen crystals. Comparisons between these three PMC, structures show that a water molecule present at a distance of 3.5 A from, the haem iron in the resting state is absent in the formic acid complex, but reappears in compound I. In addition, movements of solvent molecules, are observed during formation of compound I in a cavity located away from, the active site, in which a glycerol molecule is replaced by a sulfate., These results give structural insights into the movement of solvent, molecules, which may be important in the enzymatic reaction.
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The structure of Proteus mirabilis catalase in complex with an inhibitor, formic acid, has been solved at 2.3 A resolution. Formic acid is a key ligand of catalase because of its ability to react with the ferric enzyme, giving a high-spin iron complex. Alternatively, it can react with two transient oxidized intermediates of the enzymatic mechanism, compounds I and II. In this work, the structures of native P. mirabilis catalase (PMC) and compound I have also been determined at high resolution (2.0 and 2.5 A, respectively) from frozen crystals. Comparisons between these three PMC structures show that a water molecule present at a distance of 3.5 A from the haem iron in the resting state is absent in the formic acid complex, but reappears in compound I. In addition, movements of solvent molecules are observed during formation of compound I in a cavity located away from the active site, in which a glycerol molecule is replaced by a sulfate. These results give structural insights into the movement of solvent molecules, which may be important in the enzymatic reaction.
==About this Structure==
==About this Structure==
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1NM0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Proteus_mirabilis Proteus mirabilis] with SO4, HEM, FMT and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Catalase Catalase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.6 1.11.1.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NM0 OCA].
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1NM0 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Proteus_mirabilis Proteus mirabilis] with <scene name='pdbligand=SO4:'>SO4</scene>, <scene name='pdbligand=HEM:'>HEM</scene>, <scene name='pdbligand=FMT:'>FMT</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Catalase Catalase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.6 1.11.1.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NM0 OCA].
==Reference==
==Reference==
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[[Category: Andreoletti, P.]]
[[Category: Andreoletti, P.]]
[[Category: Gouet, P.]]
[[Category: Gouet, P.]]
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[[Category: Jouve, H.M.]]
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[[Category: Jouve, H M.]]
[[Category: Pernoud, A.]]
[[Category: Pernoud, A.]]
[[Category: FMT]]
[[Category: FMT]]
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[[Category: alpha+beta]]
[[Category: alpha+beta]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:22:49 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:07:33 2008''

Revision as of 12:07, 21 February 2008


1nm0, resolution 2.30Å

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Proteus mirabilis catalase in complex with formiate

Overview

The structure of Proteus mirabilis catalase in complex with an inhibitor, formic acid, has been solved at 2.3 A resolution. Formic acid is a key ligand of catalase because of its ability to react with the ferric enzyme, giving a high-spin iron complex. Alternatively, it can react with two transient oxidized intermediates of the enzymatic mechanism, compounds I and II. In this work, the structures of native P. mirabilis catalase (PMC) and compound I have also been determined at high resolution (2.0 and 2.5 A, respectively) from frozen crystals. Comparisons between these three PMC structures show that a water molecule present at a distance of 3.5 A from the haem iron in the resting state is absent in the formic acid complex, but reappears in compound I. In addition, movements of solvent molecules are observed during formation of compound I in a cavity located away from the active site, in which a glycerol molecule is replaced by a sulfate. These results give structural insights into the movement of solvent molecules, which may be important in the enzymatic reaction.

About this Structure

1NM0 is a Single protein structure of sequence from Proteus mirabilis with , , and as ligands. Active as Catalase, with EC number 1.11.1.6 Full crystallographic information is available from OCA.

Reference

Structural studies of Proteus mirabilis catalase in its ground state, oxidized state and in complex with formic acid., Andreoletti P, Pernoud A, Sainz G, Gouet P, Jouve HM, Acta Crystallogr D Biol Crystallogr. 2003 Dec;59(Pt 12):2163-8. Epub 2003, Nov 27. PMID:14646074

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