9w2b: Difference between revisions
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The entry | ==Tspan-7 dimer in retraction fibers== | ||
<StructureSection load='9w2b' size='340' side='right'caption='[[9w2b]], [[Resolution|resolution]] 5.87Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[9w2b]] is a 2 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=9W2B OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9W2B FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 5.87Å</td></tr> | |||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9w2b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9w2b OCA], [https://pdbe.org/9w2b PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9w2b RCSB], [https://www.ebi.ac.uk/pdbsum/9w2b PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9w2b 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]] | |||
Latest revision as of 07:31, 8 July 2026
Tspan-7 dimer in retraction fibers
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