5k7s

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'''Unreleased structure'''
 
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The entry 5k7s is ON HOLD until Paper Publication
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==MicroED structure of proteinase K at 1.6 A resolution==
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<StructureSection load='5k7s' size='340' side='right' caption='[[5k7s]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5k7s]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Engyodontium_album Engyodontium album]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5K7S OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5K7S FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5k7n|5k7n]], [[5k7o|5k7o]], [[5k7p|5k7p]], [[5k7q|5k7q]], [[5k7r|5k7r]], [[5k7t|5k7t]]</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Peptidase_K Peptidase K], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.64 3.4.21.64] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5k7s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5k7s OCA], [http://pdbe.org/5k7s PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5k7s RCSB], [http://www.ebi.ac.uk/pdbsum/5k7s PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5k7s ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/PRTK_ENGAL PRTK_ENGAL]] Hydrolyzes keratin at aromatic and hydrophobic residues.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Traditionally, crystallographic analysis of macromolecules has depended on large, well-ordered crystals, which often require significant effort to obtain. Even sizable crystals sometimes suffer from pathologies that render them inappropriate for high-resolution structure determination. Here we show that fragmentation of large, imperfect crystals into microcrystals or nanocrystals can provide a simple path for high-resolution structure determination by the cryoEM method MicroED and potentially by serial femtosecond crystallography.
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Authors:
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Atomic-resolution structures from fragmented protein crystals with the cryoEM method MicroED.,de la Cruz MJ, Hattne J, Shi D, Seidler P, Rodriguez J, Reyes FE, Sawaya MR, Cascio D, Weiss SC, Kim SK, Hinck CS, Hinck AP, Calero G, Eisenberg D, Gonen T Nat Methods. 2017 Feb 13;14(4):399-402. doi: 10.1038/nmeth.4178. PMID:28192420<ref>PMID:28192420</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 5k7s" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Engyodontium album]]
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[[Category: Peptidase K]]
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[[Category: Cascio, D]]
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[[Category: Cruz, M J.de la]]
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[[Category: Eisenberg, D]]
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[[Category: Gonen, T]]
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[[Category: Hattne, J]]
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[[Category: Reyes, F E]]
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[[Category: Rodriguez, J]]
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[[Category: Sawaya, M R]]
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[[Category: Seidler, P]]
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[[Category: Shi, D]]
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[[Category: Hydrolase]]

Revision as of 13:22, 5 April 2017

MicroED structure of proteinase K at 1.6 A resolution

5k7s, resolution 1.60Å

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