3TOU

Crystal structure of GLUTATHIONE TRANSFERASE (TARGET EFI-501058) from Ralstonia solanacearum GMI1000 with GSH bound


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.75 Å
  • R-Value Free: 0.199 
  • R-Value Work: 0.174 
  • R-Value Observed: 0.175 

wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.4 of the entry. See complete history


Literature

Crystal structure of GLUTATHIONE S-TRANSFERASE from Ralstonia solanacearum

Patskovsky, Y.Toro, R.Bhosle, R.Zencheck, W.D.Hillerich, B.Washington, R.D.Scott Glenn, A.Chowdhury, S.Evans, B.Hammonds, J.Imker, H.J.Armstrong, R.N.Gerlt, J.A.Almo, S.C.

To be published.

Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Glutathione s-transferase protein
A, B
226Ralstonia solanacearumMutation(s): 0 
Gene Names: gstKRSc2721
EC: 2.5.1.18
UniProt
Find proteins for Q8XVV6 (Ralstonia nicotianae (strain GMI1000))
Explore Q8XVV6 
Go to UniProtKB:  Q8XVV6
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupQ8XVV6
Sequence Annotations
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  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.75 Å
  • R-Value Free: 0.199 
  • R-Value Work: 0.174 
  • R-Value Observed: 0.175 
  • Space Group: P 41 21 2
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 76.475α = 90
b = 76.475β = 90
c = 151.8γ = 90
Software Package:
Software NamePurpose
PHASERphasing
REFMACrefinement
HKL-2000data reduction
HKL-2000data scaling

Structure Validation

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Ligand Structure Quality Assessment 


Entry History 

Revision History  (Full details and data files)

  • Version 1.0: 2011-09-21
    Type: Initial release
  • Version 1.1: 2011-12-21
    Changes: Non-polymer description
  • Version 1.2: 2012-02-29
    Changes: Database references, Structure summary
  • Version 1.3: 2018-01-24
    Changes: Structure summary
  • Version 1.4: 2023-09-13
    Changes: Data collection, Database references, Derived calculations, Refinement description