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1A5M

K217A VARIANT OF KLEBSIELLA AEROGENES UREASE

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]298
Detector technologyAREA DETECTOR
Collection date1996-08
DetectorXUONG-HAMLIN MULTIWIRE
Spacegroup nameI 21 3
Unit cell lengths170.800, 170.800, 170.800
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 2.000
R-factor0.194
Rwork0.194
Structure solution methodDIFFERENCE FOURIER
RMSD bond length0.006
RMSD bond angle24.830

*

Data reduction softwareSDMS
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]2.070
High resolution limit [Å]2.0002.000
Rmerge0.083

*

0.336

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Number of reflections48752
<I/σ(I)>7.52
Completeness [%]90.059
Redundancy1.81.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.525

*

PROTEIN WAS CRYSTALLIZED FROM 100 MM HEPES, PH 7.5, 1.6 M LI2SO4
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropurease5 (mg/ml)
21dropTris-HCl10 (mM)
31dropEDTA0.5 (mM)
41dropbeta-mercaptoethanol0.5 (mM)
51drop0.75-0.85 (M)
61dropHEPES50 (mM)
71reservoir1.5-1.7 (M)
81reservoirHEPES100 (mM)

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