6ybo
From Proteopedia
(Difference between revisions)
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==RT structure of Glucose Isomerase obtained at 1.06 A resolution from crystal grown in a Kapton microchip.== | ==RT structure of Glucose Isomerase obtained at 1.06 A resolution from crystal grown in a Kapton microchip.== | ||
- | <StructureSection load='6ybo' size='340' side='right'caption='[[6ybo]]' scene=''> | + | <StructureSection load='6ybo' size='340' side='right'caption='[[6ybo]], [[Resolution|resolution]] 1.06Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YBO OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6YBO FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6ybo]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Streptomyces_rubiginosus Streptomyces rubiginosus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6YBO OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6YBO FirstGlance]. <br> |
- | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6ybo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ybo OCA], [http://pdbe.org/6ybo PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ybo RCSB], [http://www.ebi.ac.uk/pdbsum/6ybo PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ybo ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr> |
+ | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6ybf|6ybf]], [[6ybi|6ybi]]</td></tr> | ||
+ | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[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] </span></td></tr> | ||
+ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6ybo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ybo OCA], [http://pdbe.org/6ybo PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ybo RCSB], [http://www.ebi.ac.uk/pdbsum/6ybo PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ybo ProSAT]</span></td></tr> | ||
</table> | </table> | ||
+ | == Function == | ||
+ | [[http://www.uniprot.org/uniprot/XYLA_STRRU XYLA_STRRU]] Involved in D-xylose catabolism. | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | Sample handling and manipulation for cryoprotection currently remain critical factors in X-ray structural determination. While several microchips for macromolecular crystallization have been proposed during the last two decades to partially overcome crystal-manipulation issues, increased background noise originating from the scattering of chip-fabrication materials has so far limited the attainable resolution of diffraction data. Here, the conception and use of low-cost, X-ray-transparent microchips for in situ crystallization and direct data collection, and structure determination at atomic resolution close to 1.0 A, is presented. The chips are fabricated by a combination of either OSTEMER and Kapton or OSTEMER and Mylar materials for the implementation of counter-diffusion crystallization experiments. Both materials produce a sufficiently low scattering background to permit atomic resolution diffraction data collection at room temperature and the generation of 3D structural models of the tested model proteins lysozyme, thaumatin and glucose isomerase. Although the high symmetry of the three model protein crystals produced almost complete data sets at high resolution, the potential of in-line data merging and scaling of the multiple crystals grown along the microfluidic channels is also presented and discussed. | ||
+ | |||
+ | Attaining atomic resolution from in situ data collection at room temperature using counter-diffusion-based low-cost microchips.,Gavira JA, Rodriguez-Ruiz I, Martinez-Rodriguez S, Basu S, Teychene S, McCarthy AA, Mueller-Dieckman C Acta Crystallogr D Struct Biol. 2020 Aug 1;76(Pt 8):751-758. doi:, 10.1107/S2059798320008475. Epub 2020 Jul 27. PMID:32744257<ref>PMID:32744257</ref> | ||
+ | |||
+ | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
+ | </div> | ||
+ | <div class="pdbe-citations 6ybo" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Gavira | + | [[Category: Streptomyces rubiginosus]] |
- | [[Category: Martinez-Rodriguez S]] | + | [[Category: Xylose isomerase]] |
+ | [[Category: Gavira, J A]] | ||
+ | [[Category: Martinez-Rodriguez, S]] | ||
+ | [[Category: D-xylose ketol isomerase]] | ||
+ | [[Category: Isomerase]] |
Revision as of 06:41, 19 August 2020
RT structure of Glucose Isomerase obtained at 1.06 A resolution from crystal grown in a Kapton microchip.
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