2mkv
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2mkv]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MKV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MKV FirstGlance]. <br> | <table><tr><td colspan='2'>[[2mkv]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MKV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2MKV FirstGlance]. <br> | ||
- | </td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2jo1|2jo1]], [[2jp3|2jp3]]</td></tr> | + | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2jo1|2jo1]], [[2jp3|2jp3]]</td></tr> |
- | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2mkv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mkv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2mkv RCSB], [http://www.ebi.ac.uk/pdbsum/2mkv 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=2mkv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mkv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2mkv RCSB], [http://www.ebi.ac.uk/pdbsum/2mkv PDBsum]</span></td></tr> |
- | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/ATNG_HUMAN ATNG_HUMAN]] Autosomal dominant primary hypomagnesemia with hypocalcuria. The disease is caused by mutations affecting the gene represented in this entry. | [[http://www.uniprot.org/uniprot/ATNG_HUMAN ATNG_HUMAN]] Autosomal dominant primary hypomagnesemia with hypocalcuria. The disease is caused by mutations affecting the gene represented in this entry. | ||
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Structure of the Na,K-ATPase regulatory protein FXYD2b in micelles: Implications for membrane-water interfacial arginines.,Gong XM, Ding Y, Yu J, Yao Y, Marassi FM Biochim Biophys Acta. 2014 May 2. pii: S0005-2736(14)00156-4. doi:, 10.1016/j.bbamem.2014.04.021. PMID:24794573<ref>PMID:24794573</ref> | Structure of the Na,K-ATPase regulatory protein FXYD2b in micelles: Implications for membrane-water interfacial arginines.,Gong XM, Ding Y, Yu J, Yao Y, Marassi FM Biochim Biophys Acta. 2014 May 2. pii: S0005-2736(14)00156-4. doi:, 10.1016/j.bbamem.2014.04.021. PMID:24794573<ref>PMID:24794573</ref> | ||
- | From | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> |
</div> | </div> | ||
== References == | == References == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: Gong, X | + | [[Category: Gong, X]] |
- | [[Category: Marassi, F M | + | [[Category: Marassi, F M]] |
[[Category: Fxyd]] | [[Category: Fxyd]] | ||
[[Category: Fxyd2b]] | [[Category: Fxyd2b]] |
Revision as of 11:18, 24 December 2014
Structure of the NA,K-ATPASE regulatory protein FXYD2b in micelles
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Categories: Gong, X | Marassi, F M | Fxyd | Fxyd2b | K-atpase | Micelle | Na | Transport protein