2lgw
From Proteopedia
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| <StructureSection load='2lgw' size='340' side='right' caption='[[2lgw]], [[NMR_Ensembles_of_Models | 15 NMR models]]' scene=''> | <StructureSection load='2lgw' size='340' side='right' caption='[[2lgw]], [[NMR_Ensembles_of_Models | 15 NMR models]]' scene=''> | ||
| == Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2lgw]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[2lgw]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LGW OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LGW FirstGlance]. <br> | 
| </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2lmg|2lmg]]</td></tr> | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2lmg|2lmg]]</td></tr> | ||
| - | <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=2lgw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lgw OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2lgw RCSB], [http://www.ebi.ac.uk/pdbsum/2lgw PDBsum]</span></td></tr> | + | <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=2lgw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lgw OCA], [http://pdbe.org/2lgw PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2lgw RCSB], [http://www.ebi.ac.uk/pdbsum/2lgw PDBsum]</span></td></tr> | 
| </table> | </table> | ||
| + | == Disease == | ||
| + | [[http://www.uniprot.org/uniprot/DNJB2_HUMAN DNJB2_HUMAN]] Young adult-onset distal hereditary motor neuropathy. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  | ||
| __TOC__ | __TOC__ | ||
| </StructureSection> | </StructureSection> | ||
| - | [[Category:  | + | [[Category: Human]] | 
| [[Category: Cao, C]] | [[Category: Cao, C]] | ||
| [[Category: Gao, X]] | [[Category: Gao, X]] | ||
Revision as of 03:11, 10 September 2015
Solution Structure of the J Domain of HSJ1a
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Categories: Human | Cao, C | Gao, X | Hu, H | Zhou, C | Chaperone | Co-chaperon | Hsj1a | J domain
