5fwb
From Proteopedia
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<StructureSection load='5fwb' size='340' side='right'caption='[[5fwb]], [[Resolution|resolution]] 1.50Å' scene=''> | <StructureSection load='5fwb' size='340' side='right'caption='[[5fwb]], [[Resolution|resolution]] 1.50Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[5fwb]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[5fwb]] is a 1 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=5FWB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5FWB FirstGlance]. <br> |
| - | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.5Å</td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5fwb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5fwb OCA], [https://pdbe.org/5fwb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5fwb RCSB], [https://www.ebi.ac.uk/pdbsum/5fwb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5fwb ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN] West syndrome. The disease is caused by mutations affecting the gene represented in this entry. |
== Function == | == Function == | ||
| - | [ | + | [https://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. |
==See Also== | ==See Also== | ||
| - | *[[Spectrin|Spectrin]] | + | *[[Spectrin 3D structures|Spectrin 3D structures]] |
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Gallego | + | [[Category: Gallego P]] |
| - | [[Category: Navarro | + | [[Category: Navarro S]] |
| - | [[Category: Reverter | + | [[Category: Reverter D]] |
| - | [[Category: Ventura | + | [[Category: Ventura S]] |
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Current revision
Human Spectrin SH3 domain D48G, E7F, K60F
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