1P7Z

Crystal structure of the D181S variant of catalase HPII from E. coli

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	ESRF BEAMLINE BM14
Synchrotron site	ESRF
Beamline	BM14
Temperature [K]	100
Detector technology	CCD
Collection date	2001-09-21
Detector	MARRESEARCH
Wavelength(s)	0.9762
Spacegroup name	P 1 21 1
Unit cell lengths	93.340, 132.880, 121.450
Unit cell angles	90.00, 109.40, 90.00

Refinement procedure

Resolution	29.800 - 2.200 *
R-factor	0.148
Rwork	0.144
R-free	0.21600 *
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	1gge
RMSD bond length	0.012
RMSD bond angle	2.000
Data reduction software	DENZO
Data scaling software	SCALEPACK
Phasing software	MOLREP
Refinement software	REFMAC

Data quality characteristics

	Overall	Outer shell
Low resolution limit [Å]	29.800	2.270
High resolution limit [Å]	2.200	2.200
Rmerge	0.100	0.330
Number of reflections	138759 *	11109 *
<I/σ(I)>	8.5	2.8
Completeness [%]	99.6	99.5
Redundancy	3.5	3.4

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, HANGING DROP	9	22 *	PEG 3350, LiCl, Tris, pH 9.0, VAPOR DIFFUSION, HANGING DROP, temperature 295.0K

Crystallization Reagents in Literatures

ID	crystal ID	solution	reagent name	concentration (unit)	details
1	1	reservoir	PEG3350	15-17 (%)
2	1	reservoir		1.6-1.7 (M)
3	1	reservoir	Tris	0.1 (M)	pH9.0