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New page: left|200px<br /><applet load="1fa6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1fa6, resolution 1.9Å" /> '''CRYSTAL STRUCTURE OF ...
 
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[[Image:1fa6.jpg|left|200px]]<br /><applet load="1fa6" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1fa6.jpg|left|200px]]<br /><applet load="1fa6" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1fa6, resolution 1.9&Aring;" />
caption="1fa6, resolution 1.9&Aring;" />
'''CRYSTAL STRUCTURE OF THE CO(II)-BOUND GLYOXALASE I OF ESCHERICHIA COLI'''<br />
'''CRYSTAL STRUCTURE OF THE CO(II)-BOUND GLYOXALASE I OF ESCHERICHIA COLI'''<br />


==Overview==
==Overview==
The metalloenzyme glyoxalase I (GlxI) converts the nonenzymatically, produced hemimercaptal of cytotoxic methylglyoxal and glutathione to, nontoxic S-D-lactoylglutathione. Human GlxI, for which the structure is, known, is active in the presence of Zn(2+). Unexpectedly, the Escherichia, coli enzyme is inactive in the presence of Zn(2+) and is maximally active, with Ni(2+). To understand this difference in metal activation and also to, obtain a representative of the bacterial enzymes, the structure of E. coli, Ni(2+)-GlxI has been determined. Structures have also been determined for, the apo enzyme as well as complexes with Co(2+), Cd(2+), and Zn(2+). It is, found that each of the protein-metal complexes that is catalytically, active has octahedral geometry. This includes the complexes of the E. coli, enzyme with Ni(2+), Co(2+), and Cd(2+), as well as the structures reported, for the human Zn(2+) enzyme. Conversely, the complex of the E. coli enzyme, with Zn(2+) has trigonal bipyramidal coordination and is inactive. This, mode of coordination includes four protein ligands plus a single water, molecule. In contrast, the coordination in the active forms of the enzyme, includes two water molecules bound to the metal ion, suggesting that this, may be a key feature of the catalytic mechanism. A comparison of the human, and E. coli enzymes suggests that there are differences between the active, sites that might be exploited for therapeutic use.
The metalloenzyme glyoxalase I (GlxI) converts the nonenzymatically produced hemimercaptal of cytotoxic methylglyoxal and glutathione to nontoxic S-D-lactoylglutathione. Human GlxI, for which the structure is known, is active in the presence of Zn(2+). Unexpectedly, the Escherichia coli enzyme is inactive in the presence of Zn(2+) and is maximally active with Ni(2+). To understand this difference in metal activation and also to obtain a representative of the bacterial enzymes, the structure of E. coli Ni(2+)-GlxI has been determined. Structures have also been determined for the apo enzyme as well as complexes with Co(2+), Cd(2+), and Zn(2+). It is found that each of the protein-metal complexes that is catalytically active has octahedral geometry. This includes the complexes of the E. coli enzyme with Ni(2+), Co(2+), and Cd(2+), as well as the structures reported for the human Zn(2+) enzyme. Conversely, the complex of the E. coli enzyme with Zn(2+) has trigonal bipyramidal coordination and is inactive. This mode of coordination includes four protein ligands plus a single water molecule. In contrast, the coordination in the active forms of the enzyme includes two water molecules bound to the metal ion, suggesting that this may be a key feature of the catalytic mechanism. A comparison of the human and E. coli enzymes suggests that there are differences between the active sites that might be exploited for therapeutic use.


==About this Structure==
==About this Structure==
1FA6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with CO as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Lactoylglutathione_lyase Lactoylglutathione lyase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.4.1.5 4.4.1.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1FA6 OCA].  
1FA6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=CO:'>CO</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Lactoylglutathione_lyase Lactoylglutathione lyase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.4.1.5 4.4.1.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1FA6 OCA].  


==Reference==
==Reference==
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[[Category: Lactoylglutathione lyase]]
[[Category: Lactoylglutathione lyase]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Clugston, S.L.]]
[[Category: Clugston, S L.]]
[[Category: He, M.M.]]
[[Category: He, M M.]]
[[Category: Honek, J.F.]]
[[Category: Honek, J F.]]
[[Category: Matthews, B.W.]]
[[Category: Matthews, B W.]]
[[Category: CO]]
[[Category: CO]]
[[Category: beta-alpha-beta-beta-beta motif]]
[[Category: beta-alpha-beta-beta-beta motif]]
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[[Category: protein-co(ii) complex]]
[[Category: protein-co(ii) complex]]


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