5SHS

CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 10 IN COMPLEX WITH c34c(n(Cc1cccc2c1cccc2)nn3)ncnc4N5CCCCC5, micromolar IC50=0.183

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	SLS BEAMLINE X10SA
Synchrotron site	SLS
Beamline	X10SA
Temperature [K]	100
Detector technology	CCD
Collection date	2008-01-31
Detector	MARMOSAIC 225 mm CCD
Wavelength(s)	0.999800
Spacegroup name	H 3
Unit cell lengths	135.350, 135.350, 235.800
Unit cell angles	90.00, 90.00, 120.00

Refinement procedure

Resolution	43.770 - 2.300
R-factor	0.1665
Rwork	0.163
R-free	0.23250
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	inhouse model
RMSD bond length	0.017
RMSD bond angle	2.230
Data reduction software	XDS
Data scaling software	XSCALE
Phasing software	PHASER
Refinement software	REFMAC (5.8.0258)

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	43.750	43.770	2.360
High resolution limit [Å]	2.300	10.290	2.300
Rmerge	0.092	0.019	0.986
Rmeas	0.107	0.022	1.147
Total number of observations	270612
Number of reflections	71486	788	5305
<I/σ(I)>	10.66	36.64	1.37
Completeness [%]	99.9	98.5	99.9
Redundancy	3.786	3.85	3.828
CC(1/2)	0.997	1.000	0.545

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP	7.5	295	5-20 mg/mL protein in 25mM HEPES/NaOH pH7.5, 150mM NaCl, 50mM BME mixed 1:1 with reservoir 0.1M HEPES/NaOH pH7.5, 30% PEG550MME, 50mM MgCl2