7v0q: Difference between revisions

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

The entry ~~7v0q is ON HOLD~~

==Local refinement of protein 4.2, class 1 of erythrocyte ankyrin-1 complex==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[7v0q]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7V0Q OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7V0Q FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.5Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7v0q FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7v0q OCA], [https://pdbe.org/7v0q PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7v0q RCSB], [https://www.ebi.ac.uk/pdbsum/7v0q PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7v0q ProSAT]</span></td></tr>

</table>

== Disease ==

[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Cali T]]

[[Category: Clarke OB]]

[[Category: Johnston JD]]

[[Category: Kim K]]

[[Category: Noble AJ]]

[[Category: Vallese F]]

[[Category: Yen LY]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 7v0q is ON HOLD
+==Local refinement of protein 4.2, class 1 of erythrocyte ankyrin-1 complex==
+<StructureSection load='7v0q' size='340' side='right'caption='[[7v0q]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[7v0q]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7V0Q OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7V0Q FirstGlance]. <br>
-Description:
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7v0q FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7v0q OCA], [https://pdbe.org/7v0q PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7v0q RCSB], [https://www.ebi.ac.uk/pdbsum/7v0q PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7v0q ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Hereditary spherocytosis. The disease is caused by variants affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/EPB42_HUMAN EPB42_HUMAN] Probably plays an important role in the regulation of erythrocyte shape and mechanical properties.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Cali T]]
+[[Category: Clarke OB]]
+[[Category: Johnston JD]]
+[[Category: Kim K]]
+[[Category: Noble AJ]]
+[[Category: Vallese F]]
+[[Category: Yen LY]]