View source for 7lm6


==Crystal structure of the Zn(II)-bound AdcAII H205L mutant variant of Streptococcus pneumoniae==
<StructureSection load='7lm6' size='340' side='right'caption='[[7lm6]], [[Resolution|resolution]] 3.37&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[7lm6]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Streptococcus_pseudopneumoniae_5247 Streptococcus pseudopneumoniae 5247]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7LM6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LM6 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.367&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=7lm6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7lm6 OCA], [https://pdbe.org/7lm6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7lm6 RCSB], [https://www.ebi.ac.uk/pdbsum/7lm6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7lm6 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/V8IJK5_9STRE V8IJK5_9STRE] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Streptococcus pneumoniae scavenges essential zinc ions from the host during colonization and infection. This is achieved by the ATP-binding cassette transporter, AdcCB, and two solute-binding proteins (SBPs), AdcA and AdcAII. It has been established that AdcAII serves a greater role during initial infection, but the molecular details of how the protein selectively acquires Zn(II) remain poorly understood. This can be attributed to the refractory nature of metal-free AdcAII to high-resolution structural determination techniques. Here, we overcome this issue by separately mutating the Zn(II)-coordinating residues and performing a combination of structural and biochemical analyses on the variant proteins. Structural analyses of Zn(II)-bound AdcAII variants revealed that specific regions within the protein underwent conformational changes via direct coupling to each of the metal-binding residues. Quantitative in vitro metal-binding assays combined with affinity determination and phenotypic growth assays revealed that each of the four Zn(II)-coordinating residues contributes to metal binding by AdcAII. Intriguingly, the phenotypic growth impact of the mutant adcAII alleles was, in general, independent of affinity, suggesting that the Zn(II)-bound conformation of the SBP is crucial for efficacious metal uptake. Collectively, these data highlight the intimate coupling of ligand affinity with protein conformational change in ligand-receptor proteins and provide a putative mechanism for AdcAII. These findings provide further mechanistic insight into the structural and functional diversity of SBPs that is broadly applicable to other prokaryotes.

Conformation of the Solute-Binding Protein AdcAII Influences Zinc Uptake in Streptococcus pneumoniae.,Zupan ML, Luo Z, Ganio K, Pederick VG, Neville SL, Deplazes E, Kobe B, McDevitt CA Front Cell Infect Microbiol. 2021 Aug 19;11:729981. doi:, 10.3389/fcimb.2021.729981. eCollection 2021. PMID:34490149<ref>PMID:34490149</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 7lm6" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Streptococcus pseudopneumoniae 5247]]
[[Category: Kobe B]]
[[Category: Luo Z]]
[[Category: McDevitt CA]]
[[Category: Zupan M]]