9w2d: Difference between revisions

Line 1:

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

The entry ~~9w2d is ON HOLD until Paper Publication~~

==Tspan7 tetramer in retraction fiber==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[9w2d]] is a 4 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=9W2D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9W2D 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]] 6.63Å</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=9w2d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9w2d OCA], [https://pdbe.org/9w2d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9w2d RCSB], [https://www.ebi.ac.uk/pdbsum/9w2d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9w2d ProSAT]</span></td></tr>

</table>

== Disease ==

[https://www.uniprot.org/uniprot/TSN7_HUMAN TSN7_HUMAN] X-linked non-syndromic intellectual disability. The disease is caused by variants affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/TSN7_HUMAN TSN7_HUMAN] May be involved in cell proliferation and cell motility.

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Jia X]]

[[Category: Li XP]]

[[Category: Liu N]]

[[Category: Wang DJ]]

[[Category: Wang HW]]

[[Category: Yu L]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 9w2d is ON HOLD  until Paper Publication
+==Tspan7 tetramer in retraction fiber==
+<StructureSection load='9w2d' size='340' side='right'caption='[[9w2d]], [[Resolution|resolution]] 6.63&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[9w2d]] is a 4 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=9W2D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9W2D 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]] 6.63&#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=9w2d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9w2d OCA], [https://pdbe.org/9w2d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9w2d RCSB], [https://www.ebi.ac.uk/pdbsum/9w2d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9w2d ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[https://www.uniprot.org/uniprot/TSN7_HUMAN TSN7_HUMAN] X-linked non-syndromic intellectual disability. The disease is caused by variants affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/TSN7_HUMAN TSN7_HUMAN] May be involved in cell proliferation and cell motility.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Jia X]]
+[[Category: Li XP]]
+[[Category: Liu N]]
+[[Category: Wang DJ]]
+[[Category: Wang HW]]
+[[Category: Yu L]]