5SFH

CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 10 IN COMPLEX WITH N(C1CC1)(C)c2nn(c(n2)CCc4nn3c(cnc(c3n4)C)C)C, micromolar IC50=0.042255

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	2012-02-05
Detector	PSI PILATUS 6M
Wavelength(s)	0.999990
Spacegroup name	H 3
Unit cell lengths	135.463, 135.463, 235.776
Unit cell angles	90.00, 90.00, 120.00

Refinement procedure

Resolution	43.750 - 2.290
R-factor	0.1762
Rwork	0.174
R-free	0.22130
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	inhouse model
RMSD bond length	0.007
RMSD bond angle	1.451
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	43.750	2.350
High resolution limit [Å]	2.290	10.240	2.290
Rmerge	0.085	0.020	1.318
Rmeas	0.095	0.022	1.465
Total number of observations	378895
Number of reflections	72627	808	5384
<I/σ(I)>	13.75	58.91	1.3
Completeness [%]	99.9	98.9	100
Redundancy	5.217	5.402	5.289
CC(1/2)	0.999	1.000	0.494

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