5AOO

X-ray structure of a human Kobuvirus: Aichi virus A (AiV)


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.10 Å
  • R-Value Work: 0.330 
  • R-Value Observed: 0.330 

wwPDB Validation   3D Report Full Report


This is version 1.2 of the entry. See complete history


Literature

The Use of Noncrystallographic Symmetry Averaging to Solve Structures from Data Affected by Perfect Hemihedral Twinning

Sabin, C.Plevka, P.

(2016) Acta Crystallogr Sect F Struct Biol Cryst Commun 72: 188

  • DOI: https://doi.org/10.1107/S2053230X16000923
  • Primary Citation of Related Structures:  
    5AOO

  • PubMed Abstract: 

    Hemihedral twinning is a crystal-growth anomaly in which a specimen is composed of two crystal domains that coincide with each other in three dimensions. However, the orientations of the crystal lattices in the two domains differ in a specific way. In diffraction data collected from hemihedrally twinned crystals, each observed intensity contains contributions from both of the domains. With perfect hemihedral twinning, the two domains have the same volumes and the observed intensities do not contain sufficient information to detwin the data. Here, the use of molecular replacement and of noncrystallographic symmetry (NCS) averaging to detwin a 2.1 Å resolution data set for Aichi virus 1 affected by perfect hemihedral twinning is described. The NCS averaging enabled the correction of errors in the detwinning introduced by the differences between the molecular-replacement model and the crystallized structure. The procedure permitted the structure to be determined from a molecular-replacement model that had 16% sequence identity and a 1.6 Å r.m.s.d. for C(α) atoms in comparison to the crystallized structure. The same approach could be used to solve other data sets affected by perfect hemihedral twinning from crystals with NCS.


  • Organizational Affiliation

    Central European Institute of Technology - Masaryk University, Kamenice 653/25, 625 00 Brno, Czech Republic.


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
VP0253Aichivirus AMutation(s): 0 
UniProt
Find proteins for O91464 (Aichi virus (strain Human/A846/88/1989))
Explore O91464 
Go to UniProtKB:  O91464
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupO91464
Sequence Annotations
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  • Reference Sequence
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 2
MoleculeChains Sequence LengthOrganismDetailsImage
VP1370Aichivirus AMutation(s): 0 
UniProt
Find proteins for O91464 (Aichi virus (strain Human/A846/88/1989))
Explore O91464 
Go to UniProtKB:  O91464
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupO91464
Sequence Annotations
Expand
  • Reference Sequence
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 3
MoleculeChains Sequence LengthOrganismDetailsImage
VP3223Aichivirus AMutation(s): 0 
UniProt
Find proteins for O91464 (Aichi virus (strain Human/A846/88/1989))
Explore O91464 
Go to UniProtKB:  O91464
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupO91464
Sequence Annotations
Expand
  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.10 Å
  • R-Value Work: 0.330 
  • R-Value Observed: 0.330 
  • Space Group: I 2 3
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 350.816α = 90
b = 350.816β = 90
c = 350.816γ = 90
Software Package:
Software NamePurpose
XDSdata reduction
GLRFphasing
MOLREPphasing
CNSrefinement

Structure Validation

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Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 2016-03-09
    Type: Initial release
  • Version 1.1: 2017-04-05
    Changes: Refinement description
  • Version 1.2: 2024-01-10
    Changes: Data collection, Database references, Derived calculations, Other, Refinement description