1xym: Difference between revisions

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New page: left|200px<br /><applet load="1xym" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xym, resolution 1.8Å" /> '''THE ROLE OF THE DIVAL...
 
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[[Image:1xym.gif|left|200px]]<br /><applet load="1xym" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1xym.gif|left|200px]]<br /><applet load="1xym" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1xym, resolution 1.8&Aring;" />
caption="1xym, resolution 1.8&Aring;" />
'''THE ROLE OF THE DIVALENT METAL ION IN SUGAR BINDING, RING OPENING, AND ISOMERIZATION BY D-XYLOSE ISOMERASE: REPLACEMENT OF A CATALYTIC METAL BY AN AMINO-ACID'''<br />
'''THE ROLE OF THE DIVALENT METAL ION IN SUGAR BINDING, RING OPENING, AND ISOMERIZATION BY D-XYLOSE ISOMERASE: REPLACEMENT OF A CATALYTIC METAL BY AN AMINO-ACID'''<br />


==Overview==
==Overview==
The distinct roles of the two magnesium ions essential to the activity of, D-xylose isomerase from Streptomyces olivochromogenes were examined. The, enzyme-magnesium complex was isolated, and the stoichiometry of cation, binding determined by neutron activation analysis to be 2 mol of magnesium, per mole of enzyme. A plot of Mg2+ added versus Mg2+ bound to enzyme is, consistent with apparent KD values of &lt; or = 0.5-1.0 mM for one Mg2+ and &lt;, or = 2-5 mM for the second. A site-directed mutant of D-xylose isomerase, was designed to remove the tighter, tetracoordinated magnesium binding, site (site 1, Mg-1); Glu180 was replaced with Lys180. The stoichiometry of, metal binding to this mutant, E180K, is 1 mol of magnesium per mole of, enzyme. Ring-opening assays with 1-thioglucose (H2S released upon ring, opening) show E180K catalyzes the opening of the sugar ring at 20% the, rate of the wild-type, but E180K does not catalyze isomerization of, glucose to fructose. Thus, the magnesium bound to Glu180 is essential for, isomerization but not essential for ring opening. The X-ray, crystallographic structures of E180K in the absence of magnesium and in, the presence and absence of 250 mM glucose were obtained to 1.8-A, resolution and refined to R factors of 17.7% and 19.7%, respectively. The, wild-type and both E180K structures show no significant structural, differences, except the epsilon-amino group of Lys180, which occupies the, position usually occupied by the Mg-1.(ABSTRACT TRUNCATED AT 250 WORDS)
The distinct roles of the two magnesium ions essential to the activity of D-xylose isomerase from Streptomyces olivochromogenes were examined. The enzyme-magnesium complex was isolated, and the stoichiometry of cation binding determined by neutron activation analysis to be 2 mol of magnesium per mole of enzyme. A plot of Mg2+ added versus Mg2+ bound to enzyme is consistent with apparent KD values of &lt; or = 0.5-1.0 mM for one Mg2+ and &lt; or = 2-5 mM for the second. A site-directed mutant of D-xylose isomerase was designed to remove the tighter, tetracoordinated magnesium binding site (site 1, Mg-1); Glu180 was replaced with Lys180. The stoichiometry of metal binding to this mutant, E180K, is 1 mol of magnesium per mole of enzyme. Ring-opening assays with 1-thioglucose (H2S released upon ring opening) show E180K catalyzes the opening of the sugar ring at 20% the rate of the wild-type, but E180K does not catalyze isomerization of glucose to fructose. Thus, the magnesium bound to Glu180 is essential for isomerization but not essential for ring opening. The X-ray crystallographic structures of E180K in the absence of magnesium and in the presence and absence of 250 mM glucose were obtained to 1.8-A resolution and refined to R factors of 17.7% and 19.7%, respectively. The wild-type and both E180K structures show no significant structural differences, except the epsilon-amino group of Lys180, which occupies the position usually occupied by the Mg-1.(ABSTRACT TRUNCATED AT 250 WORDS)


==About this Structure==
==About this Structure==
1XYM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptomyces_olivochromogenes Streptomyces olivochromogenes] with GLO, MG and OH as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Xylose_isomerase Xylose isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.5 5.3.1.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1XYM OCA].  
1XYM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptomyces_olivochromogenes Streptomyces olivochromogenes] with <scene name='pdbligand=GLO:'>GLO</scene>, <scene name='pdbligand=MG:'>MG</scene> and <scene name='pdbligand=OH:'>OH</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Xylose_isomerase Xylose isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.5 5.3.1.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XYM OCA].  


==Reference==
==Reference==
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[[Category: Streptomyces olivochromogenes]]
[[Category: Streptomyces olivochromogenes]]
[[Category: Xylose isomerase]]
[[Category: Xylose isomerase]]
[[Category: Allen, K.N.]]
[[Category: Allen, K N.]]
[[Category: Lavie, A.]]
[[Category: Lavie, A.]]
[[Category: Petsko, G.A.]]
[[Category: Petsko, G A.]]
[[Category: Ringe, D.]]
[[Category: Ringe, D.]]
[[Category: GLO]]
[[Category: GLO]]
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[[Category: isomerase(intramolecular oxidoreductase)]]
[[Category: isomerase(intramolecular oxidoreductase)]]


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