4g3n

</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=4g3n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4g3n OCA], [https://pdbe.org/4g3n PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4g3n RCSB], [https://www.ebi.ac.uk/pdbsum/4g3n PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4g3n ProSAT]</span></td></tr>

<div style="background-color:#fffaf0;">

== Publication Abstract from PubMed ==

In contrast to most bacteria which possess two type II topoisomerases (Topo IV and DNA gyrase), Mycobacterium tuberculosis possesses only one, DNA gyrase, which is functionally a hybrid enzyme. Functional differences between the two type IIA topoisomerases are thought to be specified by a C-terminal DNA binding domain (CTD) which controls DNA recognition. To explore the molecular mechanism responsible for the hybrid functions of the M. tuberculosis DNA gyrase, we conducted a series of sequence analyses and structural and biochemical experiments with the isolated GyrA CTD and the holoenzyme. While the CTD displayed a global structure similar to that of bona fide GyrA and ParC paralogs, it harbors a second key motif similar in all respects to that of the conserved GyrA-box sequence motif. Biochemical assays showed that the GyrA-box is responsible for DNA supercoiling, whereas the second GyrA-box-like motif (GyrA-box-l) is responsible for the enhanced decatenation activity suggesting that the mechanistic originality of M. tuberculosis DNA gyrase depends largely on the particular DNA path around the CTD allowed for by the presence of GyrA-box-l. Our results provide also, through phylogenetic exploration of the entire Corynebacterineae suborder, new and broader insight into the functional diversity of bacterial type IIA topoisomerases.

The Mycobacterium tuberculosis DNA gyrase possesses two functional GyrA-boxes.,Bouige A, Darmon A, Piton J, Roue M, Petrella S, Capton E, Forterre P, Aubry A, Mayer C Biochem J. 2013 Jul 22. PMID:23869946<ref>PMID:23869946</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>

</div>

<div class="pdbe-citations 4g3n" style="background-color:#fffaf0;"></div>

== References ==

<references/>