dc.contributor.author | Amado, Eric | |
dc.contributor.author | Muth, Gunther | |
dc.contributor.author | Arechaga Iturregui, Ignacio María | |
dc.contributor.author | Cabezón Navarro, María Elena | |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2019-12-16T16:08:14Z | |
dc.date.available | 2020-03-01T03:45:16Z | |
dc.date.issued | 2019-03 | |
dc.identifier.issn | 0021-9258 | |
dc.identifier.issn | 1083-351X | |
dc.identifier.other | BFU2016-78521-R | es_ES |
dc.identifier.uri | http://hdl.handle.net/10902/17587 | |
dc.description.abstract | TraB is an FtsK-like DNA translocase responsible for conjugative plasmid transfer in mycelial Streptomyces Unlike other conjugative systems, which depend on a type IV secretion system, Streptomyces requires only TraB protein to transfer the plasmid as dsDNA. The ?-domain of this protein specifically binds to repeated 8-bp motifs on the plasmid sequence, following a mechanism that is reminiscent of the FtsK/SpoIIIE chromosome segregation system. In this work, we purified and characterized the enzymatic activity of TraB, revealing that it is a DNA-dependent ATPase that is highly stimulated by dsDNA substrates. Interestingly, we found that unlike the SpoIIIE protein, the ?-domain of TraB does not confer sequence-specific ATPase stimulation. We also found that TraB binds G-quadruplex DNA structures with higher affinity than TraB-recognition sequences (TRSs). An EM-based structural analysis revealed that TraB tends to assemble as large complexes comprising four TraB hexamers, which might be a prerequisite for DNA translocation across cell membranes. In summary, our findings shed light on the molecular mechanism used by the DNA-translocating motor TraB, which may be shared by other membrane-associated machineries involved in DNA binding and translocation. | es_ES |
dc.description.sponsorship | Funding: This work was supported by the Spanish Ministerio de Economia y Competitividad (MINECO) grants BFU2016-78521-R (to E.C. and I.A.) and Deutsche Forschungsgemeinschaft SFB766 (to G.M). | es_ES |
dc.format.extent | 20 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | American Society for Biochemistry and Molecular Biology Inc. | es_ES |
dc.rights | © 2019 Amado et al. This research was originally published in Amado, Eric, et al. «The FtsK-like Motor TraB Is a DNA-Dependent ATPase That Forms Higher-Order Assemblies». Journal of Biological Chemistry, vol. 294, n.o 13, marzo de 2019, pp. 5050-59. | es_ES |
dc.source | J Biol Chem. 2019 Mar 29;294(13):5050-5059 | es_ES |
dc.subject.other | ATPase | es_ES |
dc.subject.other | DNA Binding Protein | es_ES |
dc.subject.other | DNA Segregation | es_ES |
dc.subject.other | DNA Translocase | es_ES |
dc.subject.other | DNA Translocation | es_ES |
dc.subject.other | DNA-Dependent ATPase | es_ES |
dc.subject.other | FtsK-Like ATPase | es_ES |
dc.subject.other | G-Guadruplex | es_ES |
dc.subject.other | Streptomyces | es_ES |
dc.subject.other | TRS Sequence | es_ES |
dc.subject.other | Antibiotics | es_ES |
dc.subject.other | Bacterial Conjugation | es_ES |
dc.subject.other | Conjugal Plasmid Transfer | es_ES |
dc.subject.other | Motor Protein | es_ES |
dc.title | The FtsK-like motor TraB is a DNA-dependent ATPase that forms higher-order assemblies | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://www.doi.org/10.1074/jbc.RA119.007459 | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.1074/jbc.RA119.007459 | |
dc.type.version | publishedVersion | es_ES |