6mhh
From Proteopedia
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==Proteus mirabilis ScsC linker (residues 39-49) deletion and N6K mutant== | ==Proteus mirabilis ScsC linker (residues 39-49) deletion and N6K mutant== | ||
| - | <StructureSection load='6mhh' size='340' side='right' | + | <StructureSection load='6mhh' size='340' side='right'caption='[[6mhh]], [[Resolution|resolution]] 2.08Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[6mhh]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MHH OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6MHH FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6mhh]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Atcc_29906 Atcc 29906]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MHH OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6MHH FirstGlance]. <br> |
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4yx8|4yx8]]</td></tr> | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4yx8|4yx8]]</td></tr> | ||
| + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PMI0440 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=584 ATCC 29906])</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=6mhh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mhh OCA], [http://pdbe.org/6mhh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6mhh RCSB], [http://www.ebi.ac.uk/pdbsum/6mhh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6mhh ProSAT]</span></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=6mhh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mhh OCA], [http://pdbe.org/6mhh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6mhh RCSB], [http://www.ebi.ac.uk/pdbsum/6mhh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6mhh ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Suppressor of copper sensitivity protein C from Proteus mirabilis (PmScsC) is a homotrimeric disulfide isomerase that plays a role in copper tolerance, which is a key virulence trait of this uropathogen. Each protomer of the enzyme has an N-terminal trimerization stem (59 residues) containing a flexible linker (11 residues) connected to a thioredoxin-fold-containing catalytic domain (163 residues). Here, two PmScsC variants, PmScsCDeltaN and PmScsCDeltaLinker, are characterized. PmScsCDeltaN is an N-terminally truncated form of the protomer with two helices of the trimerization stem removed, generating a protein with dithiol oxidase rather than disulfide isomerase activity. The crystal structure of PmScsCDeltaN reported here reveals, as expected, a monomer that is structurally similar to the catalytic domain of native PmScsC. The second variant, PmScsCDeltaLinker, was designed to remove the 11-amino-acid linker, and it is shown that it generates a protein that has neither disulfide isomerase nor dithiol oxidase activity. The crystal structure of PmScsCDeltaLinker reveals a trimeric arrangement, with the catalytic domains packed together very closely. Small-angle X-ray scattering analysis found that native PmScsC is predominantly trimeric in solution even at low concentrations, whereas PmScsCDeltaLinker exists as an equilibrium between monomeric, dimeric and trimeric states, with the monomeric form dominating at low concentrations. These findings increase the understanding of disulfide isomerase activity, showing how (i) oligomerization, (ii) the spacing between and (iii) the dynamic motion of catalytic domains in PmScsC all contribute to its native function. | ||
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| + | Engineered variants provide new insight into the structural properties important for activity of the highly dynamic, trimeric protein disulfide isomerase ScsC from Proteus mirabilis.,Furlong EJ, Kurth F, Premkumar L, Whitten AE, Martin JL Acta Crystallogr D Struct Biol. 2019 Mar 1;75(Pt 3):296-307. doi:, 10.1107/S2059798319000081. Epub 2019 Feb 26. PMID:30950400<ref>PMID:30950400</ref> | ||
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| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 6mhh" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Atcc 29906]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Furlong, E J]] | [[Category: Furlong, E J]] | ||
[[Category: Martin, J L]] | [[Category: Martin, J L]] | ||
Revision as of 07:01, 17 April 2019
Proteus mirabilis ScsC linker (residues 39-49) deletion and N6K mutant
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