5kef: Difference between revisions

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'''Unreleased structure'''


The entry 5kef is ON HOLD  until Paper Publication
==Structure of hypothetical Staphylococcus protein SA0856 with zinc==
<StructureSection load='5kef' size='340' side='right' caption='[[5kef]], [[Resolution|resolution]] 2.23&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5kef]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5KEF OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5KEF FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3l20|3l20]]</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=5kef FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5kef OCA], [http://pdbe.org/5kef PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5kef RCSB], [http://www.ebi.ac.uk/pdbsum/5kef PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5kef ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The crystal structures of protein SA0856 from Staphylococcus aureus in its apo-form and in complex with a Zn2+-ion have been presented. The 152 amino acid protein consists of two similar domains with alpha + beta topology. In both crystalline state and in solution, the protein forms a dimer with monomers related by a twofold pseudo-symmetry rotation axis. A sequence homology search identified the protein as a member of the structural family Glyoxalase I. We have shown that the enzyme possesses glyoxalase I activity in the presence of Zn2+, Mg2+, Ni2+, and Co2+, in this order of preference. Sequence and structure comparisons revealed that human glyoxalase I should be assigned to a subfamily A, while S. aureus glyoxalase I represents a new subfamily B, which includes also proteins from other bacteria. Both subfamilies have a similar protein chain fold but rather diverse sequences. The active sites of human and staphylococcus glyoxalases I are also different: the former contains one Zn-ion per chain; the latter incorporates two of these ions. In the active site of SA0856, the first Zn-ion is well coordinated by His58, Glu60 from basic molecule and Glu40*, His44* from adjacent symmetry-related molecule. The second Zn3-ion is coordinated only by residue His143 from protein molecule and one acetate ion. We suggest that only single Zn1-ion plays the role of catalytic center. The newly found differences between the two subfamilies could guide the design of new drugs against S. aureus, an important pathogenic micro-organism.


Authors:  
Crystal structure of Staphylococcus aureus Zn-glyoxalase I: new subfamily of glyoxalase I family.,Chirgadze YN, Boshkova EA, Battaile KP, Mendes VG, Lam R, Chan TS, Romanov V, Pai EF, Chirgadze NY J Biomol Struct Dyn. 2017 Jan 16:1-11. doi: 10.1080/07391102.2016.1278038. PMID:28034013<ref>PMID:28034013</ref>


Description:  
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
<div class="pdbe-citations 5kef" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Battaile, K P]]
[[Category: Chan, T]]
[[Category: Chirgadze, N Y]]
[[Category: Chirgadze, Y N]]
[[Category: Lam, R]]
[[Category: Mendez, V]]
[[Category: Mihajlovic, V]]
[[Category: Pai, E]]
[[Category: Romanov, V]]
[[Category: Glyoxalase]]
[[Category: Metal binding protein]]
[[Category: Metalloprotein]]

Revision as of 16:07, 18 January 2017

Structure of hypothetical Staphylococcus protein SA0856 with zinc

5kef, resolution 2.23Å

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