2osx

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(New page: 200px<br /><applet load="2osx" size="350" color="white" frame="true" align="right" spinBox="true" caption="2osx, resolution 1.100&Aring;" /> '''Endo-glycoceramidas...)
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[[Image:2osx.jpg|left|200px]]<br /><applet load="2osx" size="350" color="white" frame="true" align="right" spinBox="true"
 
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caption="2osx, resolution 1.100&Aring;" />
 
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'''Endo-glycoceramidase II from Rhodococcus sp.: Ganglioside GM3 Complex'''<br />
 
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==Overview==
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==Endo-glycoceramidase II from Rhodococcus sp.: Ganglioside GM3 Complex==
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endo-Glycoceramidase, a membrane-associated family 5 glycosidase, deviates, from the typical polysaccharide substrate specificity of other soluble, members of the family, preferentially hydrolyzing glycosidic linkages, between the oligosaccharide and ceramide moieties of gangliosides. Here we, report the first x-ray crystal structures of an endo-glycoceramidase from, Rhodococcus sp., in the apo form, in complex with the ganglioside G(M3), (Svennerholm ganglioside nomenclature (Svennerholm, L. (1964) J. Lipid, Res. 5, 145-155)), and trapped as a glycosyl-enzyme intermediate. These, snapshots provide the first molecular insight into enzyme recognition and, association with gangliosides, revealing the structural adaptations, necessary for glycosidase-catalyzed hydrolysis and detailing a novel, ganglioside binding topology. Consistent with the chemical duality of the, substrate, the active site of endo-glycoceramidase is split into a wide, polar cavity to bind the polyhydroxylated oligosaccharide moiety and a, narrow, hydrophobic tunnel to bind the ceramide lipid chains. The specific, interactions with the ceramide polar head group manifest a surprising, aglycone specificity, an observation substantiated by our kinetic, analyses. Collectively, the reported structural and kinetic data provide, insight toward rational redesign of the synthetic glycosynthase mutant of, endo-glycoceramidase to enable facile synthesis of nonnatural, therapeutically useful gangliosides.
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<StructureSection load='2osx' size='340' side='right'caption='[[2osx]], [[Resolution|resolution]] 1.10&Aring;' scene=''>
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== Structural highlights ==
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==About this Structure==
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<table><tr><td colspan='2'>[[2osx]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Rhodococcus_sp. Rhodococcus sp.]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2OSX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2OSX FirstGlance]. <br>
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2OSX is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rhodococcus_sp. Rhodococcus sp.] with <scene name='pdbligand=NA:'>NA</scene>, <scene name='pdbligand=16C:'>16C</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Endoglycosylceramidase Endoglycosylceramidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.123 3.2.1.123] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2OSX OCA].
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.1&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=16C:N-((E,2S,3R)-1,3-DIHYDROXYOCTADEC-4-EN-2-YL)PALMITAMIDE'>16C</scene>, <scene name='pdbligand=BGC:BETA-D-GLUCOSE'>BGC</scene>, <scene name='pdbligand=GAL:BETA-D-GALACTOSE'>GAL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=SIA:O-SIALIC+ACID'>SIA</scene></td></tr>
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==Reference==
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2osx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2osx OCA], [https://pdbe.org/2osx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2osx RCSB], [https://www.ebi.ac.uk/pdbsum/2osx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2osx ProSAT]</span></td></tr>
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Structural and mechanistic analyses of endo-glycoceramidase II, a membrane-associated family 5 glycosidase in the Apo and GM3 ganglioside-bound forms., Caines ME, Vaughan MD, Tarling CA, Hancock SM, Warren RA, Withers SG, Strynadka NC, J Biol Chem. 2007 May 11;282(19):14300-8. Epub 2007 Feb 28. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17329247 17329247]
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</table>
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[[Category: Endoglycosylceramidase]]
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== Function ==
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[[Category: Rhodococcus sp.]]
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[https://www.uniprot.org/uniprot/O33853_RHOSO O33853_RHOSO]
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[[Category: Single protein]]
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== Evolutionary Conservation ==
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[[Category: Caines, M.E.C.]]
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[[Image:Consurf_key_small.gif|200px|right]]
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[[Category: Strynadka, N.C.J.]]
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Check<jmol>
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[[Category: 16C]]
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<jmolCheckbox>
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[[Category: GOL]]
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/os/2osx_consurf.spt"</scriptWhenChecked>
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[[Category: NA]]
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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[[Category: (alpha/beta)8 (tim) barrel]]
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 15:04:42 2008''
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2osx ConSurf].
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<div style="clear:both"></div>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Rhodococcus sp]]
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[[Category: Caines MEC]]
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[[Category: Strynadka NCJ]]

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Endo-glycoceramidase II from Rhodococcus sp.: Ganglioside GM3 Complex

PDB ID 2osx

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