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New page: left|200px<br /><applet load="2ddr" size="450" color="white" frame="true" align="right" spinBox="true" caption="2ddr, resolution 1.40Å" /> '''Crystal structure of...
 
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[[Image:2ddr.gif|left|200px]]<br /><applet load="2ddr" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2ddr.gif|left|200px]]<br /><applet load="2ddr" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2ddr, resolution 1.40&Aring;" />
caption="2ddr, resolution 1.40&Aring;" />
'''Crystal structure of sphingomyelinase from Bacillus cereus with calcium ion'''<br />
'''Crystal structure of sphingomyelinase from Bacillus cereus with calcium ion'''<br />


==Overview==
==Overview==
Sphingomyelinase (SMase) from Bacillus cereus (Bc-SMase) hydrolyzes, sphingomyelin to phosphocholine and ceramide in a divalent metal, ion-dependent manner. Bc-SMase is a homologue of mammalian neutral SMase, (nSMase) and mimics the actions of the endogenous mammalian nSMase in, causing differentiation, development, aging, and apoptosis. Thus Bc-SMase, may be a good model for the poorly characterized mammalian nSMase. The, metal ion activation of sphingomyelinase activity of Bc-SMase was in the, order Co2+ &gt; or = Mn2+ &gt; or = Mg2+ &gt;&gt; Ca2+ &gt; or = Sr2+. The first crystal, structures of Bc-SMase bound to Co2+, Mg2+, or Ca2+ were determined. The, water-bridged double divalent metal ions at the center of the cleft in, both the Co2+- and Mg2+-bound forms were concluded to be the catalytic, architecture required for sphingomyelinase activity. In contrast, the, architecture of Ca2+ binding at the site showed only one binding site. A, further single metal-binding site exists at one side edge of the cleft., Based on the highly conserved nature of the residues of the binding sites, the crystal structure of Bc-SMase with bound Mg2+ or Co2+ may provide a, common structural framework applicable to phosphohydrolases belonging to, the DNase I-like folding superfamily. In addition, the structural features, and site-directed mutagenesis suggest that the specific beta-hairpin with, the aromatic amino acid residues participates in binding to the, membrane-bound sphingomyelin substrate.
Sphingomyelinase (SMase) from Bacillus cereus (Bc-SMase) hydrolyzes sphingomyelin to phosphocholine and ceramide in a divalent metal ion-dependent manner. Bc-SMase is a homologue of mammalian neutral SMase (nSMase) and mimics the actions of the endogenous mammalian nSMase in causing differentiation, development, aging, and apoptosis. Thus Bc-SMase may be a good model for the poorly characterized mammalian nSMase. The metal ion activation of sphingomyelinase activity of Bc-SMase was in the order Co2+ &gt; or = Mn2+ &gt; or = Mg2+ &gt;&gt; Ca2+ &gt; or = Sr2+. The first crystal structures of Bc-SMase bound to Co2+, Mg2+, or Ca2+ were determined. The water-bridged double divalent metal ions at the center of the cleft in both the Co2+- and Mg2+-bound forms were concluded to be the catalytic architecture required for sphingomyelinase activity. In contrast, the architecture of Ca2+ binding at the site showed only one binding site. A further single metal-binding site exists at one side edge of the cleft. Based on the highly conserved nature of the residues of the binding sites, the crystal structure of Bc-SMase with bound Mg2+ or Co2+ may provide a common structural framework applicable to phosphohydrolases belonging to the DNase I-like folding superfamily. In addition, the structural features and site-directed mutagenesis suggest that the specific beta-hairpin with the aromatic amino acid residues participates in binding to the membrane-bound sphingomyelin substrate.


==About this Structure==
==About this Structure==
2DDR is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_cereus Bacillus cereus] with CA as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Sphingomyelin_phosphodiesterase Sphingomyelin phosphodiesterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.4.12 3.1.4.12] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2DDR OCA].  
2DDR is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_cereus Bacillus cereus] with <scene name='pdbligand=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Sphingomyelin_phosphodiesterase Sphingomyelin phosphodiesterase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.4.12 3.1.4.12] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2DDR OCA].  


==Reference==
==Reference==
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[[Category: Ochi, S.]]
[[Category: Ochi, S.]]
[[Category: Oda, M.]]
[[Category: Oda, M.]]
[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Sakurai, J.]]
[[Category: Sakurai, J.]]
[[Category: Takahashi, M.]]
[[Category: Takahashi, M.]]
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[[Category: structural genomics]]
[[Category: structural genomics]]


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