5HIK

Crystal structure of glycine sarcosine N-methyltransferase from Methanohalophilus portucalensis in complex with S-adenosylmethionine

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	NSRRC BEAMLINE BL13C1
Synchrotron site	NSRRC
Beamline	BL13C1
Temperature [K]	100
Detector technology	CCD
Collection date	2012-04-18
Detector	ADSC QUANTUM 210
Wavelength(s)	0.97622
Spacegroup name	I 2 2 2
Unit cell lengths	51.906, 120.970, 131.789
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	27.486 - 2.354
R-factor	0.1686
Rwork	0.166
R-free	0.21420
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	5hil
RMSD bond length	0.007
RMSD bond angle	1.035
Data scaling software	HKL-2000
Refinement software	PHENIX (1.9_1692)

Data quality characteristics

	Overall	Outer shell
Low resolution limit [Å]	30.000	2.430
High resolution limit [Å]	2.350	2.350
Number of reflections	17545
<I/σ(I)>	22.8	4.9
Completeness [%]	99.9	100
Redundancy	4.6	4.8

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, HANGING DROP		277.15	Protein solution: GSMT (6.6 mg/ml) in 100 mM TES pH 7.3, 2 M KCl, 1 mM EDTA, 1 mM 2-Mercaptoethanol, 0.1 mM SAH and 0.2 M betaine. Crystallization reagent: 0.1 M Tris-HCl pH 8.5 and 1.5 M sodium chloride. SAM was soaked into crystals before data collection.