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PDBsum entry 1v7s

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Hydrolase PDB id
1v7s

 

 

 

 

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Contents
Protein chain
129 a.a. *
Ligands
NO3 ×7
Waters ×161
* Residue conservation analysis
PDB id:
1v7s
Name: Hydrolase
Title: Triclinic hen lysozyme crystallized at 313k from a d2o solution
Structure: LysozymE C. Chain: a. Synonym: 1,4-beta-n-acetylmuramidasE C, allergen gal d 4, gal d iv. Ec: 3.2.1.17
Source: Gallus gallus. Chicken. Organism_taxid: 9031. Tissue: egg white
Resolution:
1.14Å     R-factor:   0.090     R-free:   0.120
Authors: K.Harata,T.Akiba
Key ref:
K.Harata and T.Akiba (2004). Phase transition of triclinic hen egg-white lysozyme crystal associated with sodium binding. Acta Crystallogr D Biol Crystallogr, 60, 630-637. PubMed id: 15039550 DOI: 10.1107/S0907444904001805
Date:
22-Dec-03     Release date:   06-Apr-04    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P00698  (LYSC_CHICK) -  Lysozyme C from Gallus gallus
Seq:
Struc:
147 a.a.
129 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.3.2.1.17  - lysozyme.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Hydrolysis of the 1,4-beta-linkages between N-acetyl-D-glucosamine and N-acetylmuramic acid in peptidoglycan heteropolymers of the prokaryotes cell walls.

 

 
DOI no: 10.1107/S0907444904001805 Acta Crystallogr D Biol Crystallogr 60:630-637 (2004)
PubMed id: 15039550  
 
 
Phase transition of triclinic hen egg-white lysozyme crystal associated with sodium binding.
K.Harata, T.Akiba.
 
  ABSTRACT  
 
A triclinic crystal of hen egg-white lysozyme obtained from a D2O solution at 313 K was transformed into a new triclinic crystal by slow release of solvent under a temperature-regulated nitrogen-gas stream. The progress of the transition was monitored by X-ray diffraction. The transition started with the appearance of strong diffuse streaks. The diffraction spots gradually fused and faded with the emergence of diffraction from the new lattice; the scattering power of the crystal fell to a resolution of 1.5 A from the initial 0.9 A resolution. At the end of the transition, the diffuse streaks disappeared and the scattering power recovered to 1.1 A resolution. The transformed crystal contained two independent molecules and the solvent content had decreased to 18% from the 32% solvent content of the native crystal. The structure was determined at 1.1 A resolution and compared with the native structure refined at the same resolution. The backbone structures of the two molecules in the transformed crystal were superimposed on the native structure with root-mean-square deviations of 0.71 and 0.96 A. A prominent structural difference was observed in the loop region of residues Ser60-Leu75. In the native crystal, a water molecule located at the centre of this helical loop forms hydrogen bonds to main-chain peptide groups. In the transformed crystal, this water molecule is replaced by a sodium ion with octahedral coordination that involves water molecules and a nitrate ion. The peptide group connecting Arg73 and Asn74 is rotated by 180 degrees so that the CO group of Arg73 can coordinate to the sodium ion. The change in the X-ray diffraction pattern during the phase transition suggests that the transition proceeds at the microcrystal level. A mechanism is proposed for the crystal transformation.
 
  Selected figure(s)  
 
Figure 2.
Figure 2 Crystal packing of the native crystal (a) and the transformed crystal (b). The structures are viewed along the a axis. The independent molecules in the asymmetric unit are shown in a red colour. The transformed crystal contains two molecules in the unit cell.
Figure 5.
Figure 5 Structure of the sodium-binding site in the native crystal (a) and the transformed crystal (b). The water molecule in the native crystal is replaced by a sodium ion in the transformed crystal. In molecule 1 a nitrate anion is directly coordinated, but in molecule 2 a nitrate ion is bound by water-mediated hydrogen bonds.
 
  The above figures are reprinted by permission from the IUCr: Acta Crystallogr D Biol Crystallogr (2004, 60, 630-637) copyright 2004.  
  Figures were selected by the author.  

 

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