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PDBsum entry 4l5o

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protein ligands metals Protein-protein interface(s) links
Transferase PDB id
4l5o

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
217 a.a.
Ligands
GSH ×3
SO4 ×6
Metals
_ZN ×2
Waters ×255
PDB id:
4l5o
Name: Transferase
Title: Crystal structure of 26 kda gst d26h mutant of clonorchis sinensis
Structure: Putative glutathione transferase. Chain: a, b, c. Engineered: yes. Mutation: yes
Source: Clonorchis sinensis. Oriental liver fluke. Organism_taxid: 79923. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.09Å     R-factor:   0.204     R-free:   0.248
Authors: Y.J.Chung,Y.H.Han
Key ref: Y.H.Han et al. (2013). Crystal structures of 26kDa Clonorchis sinensis glutathione S-transferase reveal zinc binding and putative metal binding. Biochem Biophys Res Commun, 438, 457-461. PubMed id: 23916611 DOI: 10.1016/j.bbrc.2013.07.102
Date:
11-Jun-13     Release date:   11-Sep-13    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q25595  (Q25595_CLOSI) -  glutathione transferase from Clonorchis sinensis
Seq:
Struc:
218 a.a.
217 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.2.5.1.18  - glutathione transferase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: RX + glutathione = an S-substituted glutathione + a halide anion + H+
RX
Bound ligand (Het Group name = GSH)
corresponds exactly
+ glutathione
= S-substituted glutathione
+ halide anion
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
DOI no: 10.1016/j.bbrc.2013.07.102 Biochem Biophys Res Commun 438:457-461 (2013)
PubMed id: 23916611  
 
 
Crystal structures of 26kDa Clonorchis sinensis glutathione S-transferase reveal zinc binding and putative metal binding.
Y.H.Han, S.J.Hong, H.K.Cheong, Y.J.Chung.
 
  ABSTRACT  
 
The crystal structures of CsGST in two different space groups revealed that Asp26 and His79 coordinate a zinc ion. In one space group, His46 of an adjacent molecule participates in the coordination within 2.0Å. In the other space group, Asp26, His79 and a water molecule coordinate a zinc ion. The CsGST-D26H structure showed that four histidine residues - His26 and His79 from one molecule and the same residues from a symmetry-related neighboring molecule - coordinate a zinc ion. The coordinated zinc ions are located between two molecules and mediate molecular contacts within the crystal.
 

 

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