6ZYE

YnaI in an open-like conformation


Experimental Data Snapshot

  • Method: ELECTRON MICROSCOPY
  • Resolution: 4.10 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

wwPDB Validation   3D Report Full Report


This is version 1.0 of the entry. See complete history


Literature

The MscS-like channel YnaI has a gating mechanism based on flexible pore helices.

Flegler, V.J.Rasmussen, A.Rao, S.Wu, N.Zenobi, R.Sansom, M.S.P.Hedrich, R.Rasmussen, T.Bottcher, B.

(2020) Proc Natl Acad Sci U S A 117: 28754-28762

  • DOI: https://doi.org/10.1073/pnas.2005641117
  • Primary Citation of Related Structures:  
    6ZYD, 6ZYE, 7A46

  • PubMed Abstract: 

    The mechanosensitive channel of small conductance (MscS) is the prototype of an evolutionarily diversified large family that fine-tunes osmoregulation but is likely to fulfill additional functions. Escherichia coli has six osmoprotective paralogs with different numbers of transmembrane helices. These helices are important for gating and sensing in MscS but the role of the additional helices in the paralogs is not understood. The medium-sized channel YnaI was extracted and delivered in native nanodiscs in closed-like and open-like conformations using the copolymer diisobutylene/maleic acid (DIBMA) for structural studies. Here we show by electron cryomicroscopy that YnaI has an extended sensor paddle that during gating relocates relative to the pore concomitant with bending of a GGxGG motif in the pore helices. YnaI is the only one of the six paralogs that has this GGxGG motif allowing the sensor paddle to move outward. Access to the pore is through a vestibule on the cytosolic side that is fenestrated by side portals. In YnaI, these portals are obstructed by aromatic side chains but are still fully hydrated and thus support conductance. For comparison with large-sized channels, we determined the structure of YbiO, which showed larger portals and a wider pore with no GGxGG motif. Further in silico comparison of MscS, YnaI, and YbiO highlighted differences in the hydrophobicity and wettability of their pores and vestibule interiors. Thus, MscS-like channels of different sizes have a common core architecture but show different gating mechanisms and fine-tuned conductive properties.


  • Organizational Affiliation

    Biocenter, Julius-Maximilians-Universität Würzburg, 97080 Würzburg, Germany.


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
YnaI,Low conductance mechanosensitive channel YnaI387Escherichia coli K-12Mutation(s): 0 
Gene Names: ynaIb1330JW1323
Membrane Entity: Yes 
UniProt
Find proteins for P0AEB5 (Escherichia coli (strain K12))
Explore P0AEB5 
Go to UniProtKB:  P0AEB5
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP0AEB5
Sequence Annotations
Expand
  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: ELECTRON MICROSCOPY
  • Resolution: 4.10 Å
  • Aggregation State: PARTICLE 
  • Reconstruction Method: SINGLE PARTICLE 

Structure Validation

View Full Validation Report



Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
German Research Foundation (DFG)GermanyBo1150/15-1
German Research Foundation (DFG)GermanyINST 93/903-1 FUGG

Revision History  (Full details and data files)

  • Version 1.0: 2020-11-25
    Type: Initial release