Journal: The EMBO Journal
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Abbreviation
EMBO J
Publisher
Wiley
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Publications 1 - 10 of 51
- All-trans retinol, vitamin D and other hydrophobic compounds bind in the axial pore of the five-stranded coiled-coil domain of cartilage oligomeric matrix proteinItem type: Journal Article
The EMBO JournalGuo, Yuan; Bozic, Damir; Malashkevich, Vladimir N.; et al. (1998) - Competing interaction partners modulate the activity of Sgs1 helicase during DNA end resectionItem type: Journal Article
The EMBO JournalKasaciunaite, Kristina; Fettes, Fergus; Levikova, Maryna; et al. (2019) - The B-box dominates SAP-1-SRF interactions in the structure of the ternary complexItem type: Journal Article
The EMBO JournalHassler, Markus; Richmond, Timothy J. (2001) - Fission yeast Cactin restricts telomere transcription and elongation by controlling Rap1 levelsItem type: Journal Article
The EMBO JournalLorenzi, Luca E.; Bah, A.; Wischnewski, H.; et al. (2015) - In situ and high-resolution cryo-EM structure of a bacterial type VI secretion system membrane complexItem type: Journal Article
The EMBO JournalRapisarda, Chiara; Cherrak, Yassine; Kooger, Romain; et al. (2019)Bacteria have evolved macromolecular machineries that secrete effectors and toxins to survive and thrive in diverse environments. The type VI secretion system (T6SS) is a contractile machine that is related to Myoviridae phages. It is composed of a phage tail‐like structure inserted in the bacterial cell envelope by a membrane complex (MC) comprising the TssJ, TssL and TssM proteins. We previously reported the low‐resolution negative‐stain electron microscopy structure of the enteroaggregative Escherichia coli MC and proposed a rotational 5‐fold symmetry with a TssJ:TssL:TssM stoichiometry of 2:2:2. Here, cryo‐electron tomography analyses of the T6SS MC confirm the 5‐fold symmetry in situ and identify the regions of the structure that insert into the bacterial membranes. A high‐resolution model obtained by single‐particle cryo‐electron microscopy highlights new features: five additional copies of TssJ, yielding a TssJ:TssL:TssM stoichiometry of 3:2:2, an 11‐residue loop in TssM, protruding inside the lumen of the MC and constituting a functionally important periplasmic gate, and hinge regions. Based on these data, we propose an updated model on MC structure and dynamics during T6SS assembly and function. - Preferential binding of an unfolded protein to DsbAItem type: Journal Article
The EMBO JournalFrech, Christian; Wunderlich, Martina; Glockshuber, Rudi; et al. (1996) - Molecular basis of the C-terminal tail-to-tail assembly of the sarcomeric filament protein myomesinItem type: Journal Article
The EMBO JournalPinotsis, Nikos; Lange, Stephan; Perriard, Jean-Claude; et al. (2008) - Corrigendum: Differential effects of viral silencing suppressors on siRNA and miRNA loading support the existence of two distinct cellular pools of ARGONAUTE1Item type: Other Journal Item
The EMBO JournalSchott, Gregory; Mari-Ordonez, Arturo; Himber, Christophe; et al. (2015) - Genome‐scale, single‐cell‐type resolution of microRNA activities within a whole plant organItem type: Journal Article
The EMBO JournalBrosnan, Christopher A.; Sarazin, Alexis; Lim, PeiQi; et al. (2019) - CD19 and BAFF-R can signal to promote B-cell survival in the absence of SykItem type: Journal Article
The EMBO JournalHobeika, Elias; Levit-Zerdoun, Ella; Anastasopoulou, Vasiliki; et al. (2015)
Publications 1 - 10 of 51