5dse: Difference between revisions

<StructureSection load='5dse' size='340' side='right'caption='[[5dse]], [[Resolution|resolution]] 2.90&Aring;' scene=''>

<table><tr><td colspan='2'>[[5dse]] 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=5DSE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5DSE FirstGlance]. <br>

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.9&#8491;</td></tr>

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5dse FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5dse OCA], [https://pdbe.org/5dse PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5dse RCSB], [https://www.ebi.ac.uk/pdbsum/5dse PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5dse ProSAT]</span></td></tr>

[https://www.uniprot.org/uniprot/HYCCI_HUMAN HYCCI_HUMAN] Hypomyelination - congenital cataract. The disease is caused by mutations affecting the gene represented in this entry.

[https://www.uniprot.org/uniprot/HYCCI_HUMAN HYCCI_HUMAN] May have a role in the beta-catenin/Lef signaling pathway. May have a role in the process of myelination of the central and peripheral nervous system.<ref>PMID:16951682</ref>  

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Baskin JM]]

[[Category: De Camilli P]]

[[Category: Reinisch KM]]

[[Category: Wu X]]