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5vh8
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 5vh8 is ON HOLD Authors: Chen, J.L., VanEtten, D.M., Fountain, M.A., Yildirim, I., Disney, M.D. Description: Structure and dynamics of RNA repeat e...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure and dynamics of RNA repeat expansions that cause Huntington's Disease and myotonic dystrophy type 1== | |
| - | + | <StructureSection load='5vh8' size='340' side='right'caption='[[5vh8]]' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5vh8]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VH8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5VH8 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5vh8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vh8 OCA], [https://pdbe.org/5vh8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5vh8 RCSB], [https://www.ebi.ac.uk/pdbsum/5vh8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5vh8 ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: | + | __TOC__ |
| - | [[Category: Fountain | + | </StructureSection> |
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: Yildirim | + | [[Category: Large Structures]] |
| + | [[Category: Chen JL]] | ||
| + | [[Category: Disney MD]] | ||
| + | [[Category: Fountain MA]] | ||
| + | [[Category: VanEtten DM]] | ||
| + | [[Category: Yildirim I]] | ||
Current revision
Structure and dynamics of RNA repeat expansions that cause Huntington's Disease and myotonic dystrophy type 1
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