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6vsv
From Proteopedia
(Difference between revisions)
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<StructureSection load='6vsv' size='340' side='right'caption='[[6vsv]], [[Resolution|resolution]] 1.62Å' scene=''> | <StructureSection load='6vsv' size='340' side='right'caption='[[6vsv]], [[Resolution|resolution]] 1.62Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[6vsv]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[6vsv]] 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=6VSV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6VSV 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]] 1.62Å</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=6vsv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6vsv OCA], [https://pdbe.org/6vsv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6vsv RCSB], [https://www.ebi.ac.uk/pdbsum/6vsv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6vsv ProSAT]</span></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=6vsv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6vsv OCA], [https://pdbe.org/6vsv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6vsv RCSB], [https://www.ebi.ac.uk/pdbsum/6vsv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6vsv ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | + | [https://www.uniprot.org/uniprot/SCN4B_HUMAN SCN4B_HUMAN] Romano-Ward syndrome. The disease is caused by mutations affecting the gene represented in this entry. | |
== Function == | == Function == | ||
| - | + | [https://www.uniprot.org/uniprot/SCN4B_HUMAN SCN4B_HUMAN] Modulates channel gating kinetics. Causes negative shifts in the voltage dependence of activation of certain alpha sodium channels, but does not affect the voltage dependence of inactivation (By similarity). | |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Das | + | [[Category: Das S]] |
| - | [[Category: Petegem | + | [[Category: Van Petegem F]] |
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Current revision
Crystal structure of a disease mutant of the Voltage-gated Sodium Channel Beta 4 subunit extracellular domain
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