• Structural basis of NPR1 in activating plant immunity
    • Structural basis of NPR1 in activating plant immunity
    • Structural basis of NPR1 in activating plant immunity

    • ,
    •   Structural basis of NPR1 in activating plant immunity We report cryo-electron microscopy and crystal structures of Arabidopsis NPR1 and its complex with the transcription factor TGA3. Cryo-electron microscopy analysis reveals that NPR1 is a bird-shaped homodimer comprising a central Broad-complex, Tramtrack and Bric-à-brac (BTB) domain, a BTB and carboxyterminal Kelch helix bundle, four ankyrin repeats and a disordered salicylic-acid-binding…
  • Fab-dimerized glycan-reactive antibodies are a structural category of natural antibodies
  • Structural Basis for Virulence Activation of Francisella tularensis
    • Structural Basis for Virulence Activation of Francisella tularensis
    • Structural Basis for Virulence Activation of Francisella tularensis

    • , ,
    •   Structural Basis for Virulence Activation of Francisella tularensis The bacterium Francisella tularensis (Ft) is one of the most infectious agents known. Ft virulence is controlled by a unique combination of transcription regulators: the MglA-SspA heterodimer, PigR, and the stress signal, ppGpp. MglA-SspA assembles with the σ70-associated RNAP holoenzyme (RNAPσ70), forming a virulence-specialized polymerase. These factors activate Francisella pathogenicity island…
  • Data-driven determination of number of discrete conformations in single-particle cryo-EM
    • Data-driven determination of number of discrete conformations in single-particle cryo-EM
    • Data-driven determination of number of discrete conformations in single-particle cryo-EM

    • , ,
    •   Data-driven determination of number of discrete conformations in single-particle cryo-EM Single-particle cryo-EM can be used to image heterogeneous samples containing multiple molecular species, different oligomeric states or distinct conformations. This, however, requires expert-user knowledge and trial-and-error experimentation to determine the correct number of conformations present in a mixture. Here, we propose an approach to address the problem of automatically…
  • Redox-sensitive E2 Rad6 controls cellular response to oxidative stress via K63-linked ubiquitination of ribosomes
  • Disruption of the HIV-1 Envelope allosteric network blocks CD4-induced rearrangements
    • Disruption of the HIV-1 Envelope allosteric network blocks CD4-induced rearrangements
    • Disruption of the HIV-1 Envelope allosteric network blocks CD4-induced rearrangements

    • , ,
    •   Disruption of the HIV-1 Envelope allosteric network blocks CD4-induced rearrangements The trimeric HIV-1 Envelope protein (Env) mediates viral-host cell fusion via a network of conformational transitions, with allosteric elements in each protomer orchestrating host receptor-induced exposure of the co-receptor binding site and fusion elements. To understand the molecular details of this allostery, here, we introduce Env mutations aimed to…
  • Accurate Detection of Proteins in Cryo-Electron Tomograms from Sparse Labels
    • Accurate Detection of Proteins in Cryo-Electron Tomograms from Sparse Labels
    • Accurate Detection of Proteins in Cryo-Electron Tomograms from Sparse Labels

    • , ,
    •   Accurate Detection of Proteins in Cryo-Electron Tomograms from Sparse Labels Cryo-electron tomography (CET) combined with sub-volume averaging (SVA), is currently the only imaging technique capable of determining the structure of proteins imaged inside cells at molecular resolution. To obtain high-resolution reconstructions, sub-volumes containing randomly distributed copies of the protein of interest need be identified, extracted and subjected to SVA,…
  • Structure and dynamics of the Arabidopsis O-fucosyltransferase SPINDLY
    • Structure and dynamics of the Arabidopsis O-fucosyltransferase SPINDLY
    • Structure and dynamics of the Arabidopsis O-fucosyltransferase SPINDLY

    • ,
    •   Structure and dynamics of the Arabidopsis O-fucosyltransferase SPINDLY SPINDLY (SPY) in Arabidopsis thaliana is a novel nucleocytoplasmic protein O-fucosyltransferase (POFUT), which regulates diverse developmental processes. Sequence analysis indicates that SPY is distinct from ER-localized POFUTs and contains N-terminal tetratricopeptide repeats (TPRs) and a C-terminal catalytic domain resembling the O-linked-N-acetylglucosamine (GlcNAc) transferases (OGTs). However, the structural feature that determines the…