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4OZA

Backbone Modifications in the Protein GB1 Helix: beta-3-Ala24, beta-3-Lys28, beta-3-Gln32, beta-3-Asp36

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU FR-E SUPERBRIGHT
Temperature [K]100
Detector technologyCCD
Collection date2012-08-30
DetectorRIGAKU SATURN 944
Wavelength(s)1.5418
Spacegroup nameI 41
Unit cell lengths65.944, 65.944, 21.896
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution23.315 - 2.201
R-factor0.2345
Rwork0.233
R-free0.26000
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2qmt
RMSD bond length0.007
RMSD bond angle1.139
Data scaling softwared*TREK
Phasing softwareCrystalClear
Refinement softwarePHENIX ((phenix.refine: 1.8_1069))
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]23.31023.3102.280
High resolution limit [Å]2.2004.7302.200
Rmerge0.1020.0720.296
Total number of observations1330316551295
Number of reflections2418
<I/σ(I)>1129.23.2
Completeness [%]96.610098.8
Redundancy5.466.055.42
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.62980.2 M calcium chloride, 0.1 M sodium acetate pH 4.6, 30% v/v isopropanol

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