2mkv: Difference between revisions

Line 1:

'''~~Unreleased structure~~'''

==Structure of the NA,K-ATPASE regulatory protein FXYD2b in micelles==

~~The entry~~ 2mkv is ~~ON HOLD~~

== 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].

~~Authors~~: ~~Marassi~~, F.M., ~~Gong~~, X.

</td></tr><tr><td class="sblockLbl">[[Related_structure|Related:]]</td><td class="sblockDat">[[2jo1|2jo1]], [[2jp3|2jp3]]</td></tr>

<tr><td class="sblockLbl">Activity:</td><td class="sblockDat">[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </td></tr>

~~Description~~: ~~Structure~~ of the NA,K-~~ATPASE regulatory~~ protein ~~FXYD2b in micelles~~

<tr><td class="sblockLbl">Resources:</td><td class="sblockDat">[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]</td></tr>

<table>

== 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.

== Function ==

[[http://www.uniprot.org/uniprot/ATNG_HUMAN ATNG_HUMAN]] May be involved in forming the receptor site for cardiac glycoside binding or may modulate the transport function of the sodium ATPase.

__TOC__

</StructureSection>

[[Category: Gong, X.]]

[[Category: Marassi, F M.]]

[[Category: Fxyd]]

[[Category: Fxyd2b]]

[[Category: K-atpase]]

[[Category: Micelle]]

[[Category: Na]]

[[Category: Transport protein]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+==Structure of the NA,K-ATPASE regulatory protein FXYD2b in micelles==
+<StructureSection load='2mkv' size='340' side='right' caption='[[2mkv]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
-The entry 2mkv is ON HOLD
+== 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]. <br>
-Authors: Marassi, F.M., Gong, X.
+</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2jo1|2jo1]], [[2jp3|2jp3]]</td></tr>
+<tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span></td></tr>
-Description: Structure of the NA,K-ATPASE regulatory protein FXYD2b in micelles
+<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>
+<table>
+== 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.
+== Function ==
+[[http://www.uniprot.org/uniprot/ATNG_HUMAN ATNG_HUMAN]] May be involved in forming the receptor site for cardiac glycoside binding or may modulate the transport function of the sodium ATPase.
+__TOC__
+</StructureSection>
+[[Category: Gong, X.]]
+[[Category: Marassi, F M.]]
+[[Category: Fxyd]]
+[[Category: Fxyd2b]]
+[[Category: K-atpase]]
+[[Category: Micelle]]
+[[Category: Na]]
+[[Category: Transport protein]]