2ddr: Difference between revisions
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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=" | [[Image:2ddr.gif|left|200px]]<br /><applet load="2ddr" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="2ddr, resolution 1.40Å" /> | caption="2ddr, resolution 1.40Å" /> | ||
'''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 | 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+ > or = Mn2+ > or = Mg2+ >> Ca2+ > 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:// | 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 | [[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]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:57:48 2008'' | ||