5fwc

<table><tr><td colspan='2'>[[5fwc]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5FWC OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5FWC FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=NH4:AMMONIUM+ION'>NH4</scene></td></tr>

<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5fw6|5fw6]], [[5fw7|5fw7]], [[5fw8|5fw8]], [[5fw9|5fw9]], [[5fwb|5fwb]]</td></tr>

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

[[http://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN]] West syndrome. The disease is caused by mutations affecting the gene represented in this entry.

[[http://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN]] Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane.

*[[Spectrin|Spectrin]]

[[Category: Human]]

[[Category: Gallego, P]]

[[Category: Navarro, S]]

[[Category: Reverter, D]]

[[Category: Ventura, S]]

[[Category: Structural protein]]