5LQN

Crystal Structure of COMT in complex with 2-[(3-chlorophenoxy)methyl]-4-methyl-5-(1H-pyrazol-5-yl)-1,3-thiazole

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	SLS BEAMLINE X10SA
Synchrotron site	SLS
Beamline	X10SA
Temperature [K]	100
Detector technology	PIXEL
Collection date	2010-11-11
Detector	PSI PILATUS 6M
Wavelength(s)	1.000000
Spacegroup name	P 21 21 21
Unit cell lengths	47.186, 59.945, 78.546
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	47.650 - 1.720
R-factor	0.1988
Rwork	0.196
R-free	0.24260
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	inhouse model
Data reduction software	XDS
Data scaling software	XSCALE
Phasing software	PHASER
Refinement software	REFMAC (5.6.0081)

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	47.650	47.650	1.760
High resolution limit [Å]	1.720	7.690	1.720
Rmerge	0.060	0.026	1.379
Number of reflections	24349
<I/σ(I)>	14.51	35.76	1.3
Completeness [%]	99.8	99.4	100
Redundancy	6.3
CC(1/2)	0.999	0.999	0.572

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP	9	295	AMMONIUM SULPHATE, CHES, PH 9