6w6z

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==BlsA ground state==
==BlsA ground state==
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<StructureSection load='6w6z' size='340' side='right'caption='[[6w6z]]' scene=''>
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<StructureSection load='6w6z' size='340' side='right'caption='[[6w6z]], [[Resolution|resolution]] 1.71&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6W6Z OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6W6Z FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6w6z]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Acinetobacter_baumannii Acinetobacter baumannii]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6W6Z OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6W6Z FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6w6z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6w6z OCA], [http://pdbe.org/6w6z PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6w6z RCSB], [http://www.ebi.ac.uk/pdbsum/6w6z PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6w6z ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.71&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FMN:FLAVIN+MONONUCLEOTIDE'>FMN</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6w6z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6w6z OCA], [https://pdbe.org/6w6z PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6w6z RCSB], [https://www.ebi.ac.uk/pdbsum/6w6z PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6w6z ProSAT]</span></td></tr>
</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/V5VB82_ACIBA V5VB82_ACIBA]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The opportunistic human pathogen, A. baumannii, senses and responds to light using the blue light sensing A (BlsA) photoreceptor protein. BlsA is a blue-light-using flavin adenine dinucleotide (BLUF) protein that is known to regulate a wide variety of cellular functions through interactions with different binding partners. Using immunoprecipitation of tagged BlsA in A. baumannii lysates, we observed a number of proteins that interact with BlsA, including several transcription factors. In addition to a known binding partner, the iron uptake regulator Fur, we identified the biofilm response regulator BfmR as a putative BlsA-binding partner. Using microscale thermophoresis, we determined that both BfmR and Fur bind to BlsA with nanomolar binding constants. To better understand how BlsA interacts with and regulates these transcription factors, we solved the X-ray crystal structures of BlsA in both a ground (dark) state and a photoactivated light state. Comparison of the light- and dark-state structures revealed that, upon photoactivation, the two alpha-helices comprising the variable domain of BlsA undergo a distinct conformational change. The flavin-binding site, however, remains largely unchanged from dark to light. These structures, along with docking studies of BlsA and Fur, reveal key mechanistic details about how BlsA propagates the photoactivation signal between protein domains and on to its binding partner. Taken together, our structural and biophysical data provide important insights into how BlsA controls signal transduction in A. baumannii and provides a likely mechanism for blue-light-dependent modulation of biofilm formation and iron uptake.
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Structural Basis for the Regulation of Biofilm Formation and Iron Uptake in A. baumannii by the Blue-Light-Using Photoreceptor, BlsA.,Chitrakar I, Iuliano JN, He Y, Woroniecka HA, Tolentino Collado J, Wint JM, Walker SG, Tonge PJ, French JB ACS Infect Dis. 2020 Sep 30. doi: 10.1021/acsinfecdis.0c00156. PMID:32926768<ref>PMID:32926768</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 6w6z" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Acinetobacter baumannii]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Chitrakar I]]
[[Category: Chitrakar I]]
[[Category: French JB]]
[[Category: French JB]]

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BlsA ground state

PDB ID 6w6z

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