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5I3H

Structure-Function Studies on Role of Hydrophobic Clamping of a Basic Glutamate in Catalysis by Triosephosphate Isomerase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]100
Detector technologyCCD
Collection date2012-06-04
DetectorRIGAKU SATURN 944+
Wavelength(s)1.5418
Spacegroup nameP 1
Unit cell lengths46.282, 46.656, 60.981
Unit cell angles72.68, 88.47, 80.60
Refinement procedure
Resolution28.470 - 2.250
R-factor0.1681
Rwork0.166
R-free0.21070
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3tim
RMSD bond length0.002
RMSD bond angle0.617
Data reduction softwared*TREK
Data scaling softwared*TREK
Phasing softwareMOLREP
Refinement softwarePHENIX (1.9_1692)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]28.4702.299
High resolution limit [Å]2.2502.250
Rmerge0.052
Number of reflections23315
<I/σ(I)>15.9
Completeness [%]98.4
Redundancy2.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP728715-25% Peg 8000, 50-100 mM potassium acetate, 100 mM BTP pH 7.0

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