View source for 22hr


==Crystal structure of Apo FtsZ from Acinetobacter baumannii==
<StructureSection load='22hr' size='340' side='right'caption='[[22hr]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[22hr]] is a 2 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=22HR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=22HR 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&#8491;</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=22hr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=22hr OCA], [https://pdbe.org/22hr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=22hr RCSB], [https://www.ebi.ac.uk/pdbsum/22hr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=22hr ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Acinetobacter baumannii is an opportunistic pathogen known for its extensive antibiotic resistance, posing a significant concern in healthcare settings. Given global concern over broad-spectrum antibiotic use and its impact on the human microbiome, targeting the bacterial cell-division protein Filamenting temperature-sensitive Z (FtsZ) is a promising strategy for developing new antibiotics, as this protein is essential for bacterial cell division. FtsZ polymerizes into filaments to form the Z-ring at the cell division site. This Z-ring orchestrates the recruitment of other crucial proteins in cytokinesis and cell wall synthesis, making it critical for bacterial viability. To target FtsZ from Acinetobacter baumannii (abFtsZ), we have elucidated the first crystal structures in the apo and GDP-bound state. The structural analysis revealed that the abFtsZ-GDP complex exists in a relaxed state conformation with weak inter-subunit interactions. The GTPase activity of abFtsZ showed a V(max) of 3.3 +/- 0.4 nmolP/nmolFtsZ/min, and a K(m) of 2.3 mM. By virtual screening using the crystal structure of abFtsZ, we identified six potential inhibitors: Gossypin, Stafib-1, Tryphostin A51, Sangivamycin, Scutellarin, and Ellagic acid that target the GTP-binding pocket. These inhibitors exhibited high docking scores ranging from -10.2 to -8.4 kcal/mol and remained stable throughout the 500 ns MD simulation. These inhibitors can serve as lead molecules for the development of a new antibacterial agent.

Crystal structure of FtsZ from Acinetobacter baumannii and identification of a potential inhibitor targeting its GTPase domain.,Yadav AK, Naz F, Singh A, Sharma S, Deka J, Madhuri M, Saini C, Kumar M, Kaur P, Singh TP, Ethayathulla AS Int J Biol Macromol. 2026 May;364:152295. doi: 10.1016/j.ijbiomac.2026.152295. , Epub 2026 Apr 30. PMID:42067083<ref>PMID:42067083</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 22hr" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Acinetobacter baumannii]]
[[Category: Large Structures]]
[[Category: Ethayathulla AS]]
[[Category: Kaur P]]
[[Category: Kumar M]]
[[Category: Madhuri M]]
[[Category: Saini C]]
[[Category: Singh A]]
[[Category: Singh TP]]
[[Category: Yadav AK]]