5Q7K

PanDDA analysis group deposition -- Crystal Structure of DCLRE1A after initial refinement with no ligand modelled (structure 193)

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	DIAMOND BEAMLINE I04-1
Synchrotron site	Diamond
Beamline	I04-1
Detector technology	PIXEL
Collection date	2017-04-11
Detector	DECTRIS PILATUS 6M
Wavelength(s)	0.92
Spacegroup name	P 21 21 21
Unit cell lengths	51.826, 58.022, 114.548
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	57.340 - 2.000
R-factor	0.2381
Rwork	0.236
R-free	0.28120
Structure solution method	FOURIER SYNTHESIS
Starting model (for MR)	5aho
RMSD bond length	0.019
RMSD bond angle	1.889
Data reduction software	XDS
Data scaling software	Aimless (0.5.31)
Phasing software	REFMAC
Refinement software	REFMAC (5.8.0155)

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	57.340	57.990	1.560
High resolution limit [Å]	1.520	6.800	1.520
Rmerge	0.061	0.024	1.235
Rmeas	0.067	0.026	1.341
Rpim	0.026	0.010	0.516
Total number of observations	338369	4335	24909
Number of reflections	52960
<I/σ(I)>	12.1	51.3	1.4
Completeness [%]	98.4	99.9	97.1
Redundancy	6.4	6.1	6.5
CC(1/2)	0.999	0.998	0.773

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP	6	298	30% PEG 1000, 0.1M MIB buffer