View source for 6fl0


==Crystal structure of the membrane attack complex assembly inhibitor BGA71 from Lyme disease agent Borreliella bavariensis==
<StructureSection load='6fl0' size='340' side='right' caption='[[6fl0]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6fl0]] is a 18 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6FL0 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6FL0 FirstGlance]. <br>
</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=6fl0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6fl0 OCA], [http://pdbe.org/6fl0 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6fl0 RCSB], [http://www.ebi.ac.uk/pdbsum/6fl0 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6fl0 ProSAT]</span></td></tr>
</table>
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== Publication Abstract from PubMed ==
Borrelia (B.) bavariensis, B. burgdorferi, B. afzelii, B. garinii, B. spielmanii, and B. mayonii are the causative agents in Lyme disease. Lyme disease spirochetes reside in infected Ixodes ticks and are transferred to mammalian hosts during tick feeding. Once transmitted, spirochetes must overcome the first line of defense of the innate immune system either by binding complement regulators or by terminating the formation of the membrane attack complex (MAC). In B. bavariensis, the proteins BGA66 and BGA71 inhibit complement activation by interacting with the late complement components C7, C8, and C9, as well as with the formed MAC. In this study, we have determined the crystal structure of the potent MAC inhibitor BGA71 at 2.9 A resolution. The structure revealed a cysteine cross-linked homodimer. Based on the crystal structure of BGA71 and the structure-based sequence alignment with CspA from B. burgdorferi, we have proposed a potential binding site for C7 and C9, both of which are constituents of the formed MAC. Our results shed light on the molecular mechanism of immune evasion developed by the human pathogenic Borrelia species to overcome innate immunity. These results will aid in the understanding of Lyme disease pathogenesis and pave the way for the development of new strategies to prevent Lyme disease.

Crystal structure of the membrane attack complex assembly inhibitor BGA71 from the Lyme disease agent Borrelia bavariensis.,Brangulis K, Akopjana I, Petrovskis I, Kazaks A, Kraiczy P, Tars K Sci Rep. 2018 Jul 26;8(1):11286. doi: 10.1038/s41598-018-29651-9. PMID:30050126<ref>PMID:30050126</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
<references/>
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</StructureSection>
[[Category: Akopjana, I]]
[[Category: Brangulis, K]]
[[Category: Kazaks, A]]
[[Category: Petrovskis, I]]
[[Category: Tars, K]]
[[Category: Complement system inhibitor]]
[[Category: Immune system]]
[[Category: Outer surface protein]]