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==Human Spectrin SH3 domain D48G, E7A, K60A== | |||
<StructureSection load='5fwc' size='340' side='right' caption='[[5fwc]], [[Resolution|resolution]] 1.40Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5fwc]] is a 1 chain structure. 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://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5FWC FirstGlance]. <br> | |||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><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://oca.weizmann.ac.il/oca-docs/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> | |||
</table> | |||
== Disease == | |||
[[http://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN]] West syndrome. The disease is caused by mutations affecting the gene represented in this entry. | |||
== Function == | |||
[[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. | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Gallego, P]] | [[Category: Gallego, P]] | ||
[[Category: Navarro, S]] | |||
[[Category: Reverter, D]] | [[Category: Reverter, D]] | ||
[[Category: Ventura, S]] | [[Category: Ventura, S]] | ||
[[Category: Spectrin sh3]] | |||
[[Category: Structural protein]] | |||
Revision as of 19:22, 2 January 2017
Human Spectrin SH3 domain D48G, E7A, K60AHuman Spectrin SH3 domain D48G, E7A, K60A
Structural highlights
Disease[SPTN1_HUMAN] West syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function[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. |
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