4h43
From Proteopedia
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==Structure of the Salmonella plasmid virulence C protein (SpvC) H106N mutant.== | ==Structure of the Salmonella plasmid virulence C protein (SpvC) H106N mutant.== | ||
- | <StructureSection load='4h43' size='340' side='right' caption='[[4h43]], [[Resolution|resolution]] 2.30Å' scene=''> | + | <StructureSection load='4h43' size='340' side='right'caption='[[4h43]], [[Resolution|resolution]] 2.30Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[4h43]] is a 2 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4h43]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Salmonella_enterica_subsp._enterica_serovar_Typhimurium_str._LT2 Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4H43 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4H43 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]] 2.304Å</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=4h43 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4h43 OCA], [https://pdbe.org/4h43 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4h43 RCSB], [https://www.ebi.ac.uk/pdbsum/4h43 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4h43 ProSAT]</span></td></tr> |
</table> | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/SPVC_SALTY SPVC_SALTY] Secreted effector that irreversibly inactivates host MAP kinases by catalyzing the dephosphorylation of the phosphothreonine residue in the pT-X-pY motif in MAPK2/ERK2, MAPK3/ERK1, and p38, via a beta-elimination reaction leading to a dehydrobutyrine residue. Is also able to remove the phosphate group from phospho-JNK in vitro, but JNK may not be a substrate in vivo. Could help suppress localized proinflammatory responses at infection foci in the spleen and liver, and thereby facilitate bacterial growth.<ref>PMID:17303758</ref> <ref>PMID:18060821</ref> <ref>PMID:18084305</ref> <ref>PMID:18284579</ref> | ||
+ | == References == | ||
+ | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: Salmonella enterica subsp. enterica serovar | + | [[Category: Large Structures]] |
- | [[Category: Hengge | + | [[Category: Salmonella enterica subsp. enterica serovar Typhimurium str. LT2]] |
- | [[Category: Johnson | + | [[Category: Hengge AC]] |
- | [[Category: Shenoy | + | [[Category: Johnson SJ]] |
- | + | [[Category: Shenoy AG]] | |
- | + | ||
- | + |
Current revision
Structure of the Salmonella plasmid virulence C protein (SpvC) H106N mutant.
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