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1BH5

HUMAN GLYOXALASE I Q33E, E172Q DOUBLE MUTANT

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-03-23
DetectorRIGAKU RAXIS
Spacegroup nameP 41
Unit cell lengths67.280, 67.280, 164.730
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.200
R-factor0.25

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Rwork0.180
R-free0.28000

*

Structure solution methodMR
Starting model (for MR)1fro
RMSD bond length0.010
RMSD bond angle0.030
Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.320
High resolution limit [Å]2.2002.200
Rmerge0.0480.128
Number of reflections33195
<I/σ(I)>275.5
Completeness [%]89.763

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Redundancy3.51.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

5.815

*

Cameron, A.D., (1997) EMBO J., 16, 3386.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropPEG200012.5-15 (%(w/v))
21dropMES25 (mM)
31drop0.05 (M)
41dropprotein6 (mg/ml)
51drop2-mercaptoethanol0.5 (%)
61dropS-benzyl-glutathione1 (mM)
71reservoirPEG200025-30 (%(w/v))
81reservoirMES50 (mM)
91reservoir0.1 (M)

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