1O24

Crystal structure of Thymidylate Synthase Complementing Protein (TM0449) from Thermotoga maritima at 2.0 A resolution

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	SSRL BEAMLINE BL9-1
Synchrotron site	SSRL
Beamline	BL9-1
Temperature [K]	100
Detector technology	CCD
Collection date	2002-04-14
Detector	ADSC QUANTUM 4
Spacegroup name	P 21 21 21
Unit cell lengths	54.480, 116.639, 142.252
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	20.000 - 2.000
Rwork	0.207
R-free	0.25200 *
Structure solution method	MR
Starting model (for MR)	1kq4
RMSD bond length	0.006
RMSD bond angle	1.230
Data reduction software	MOSFLM
Data scaling software	SCALA
Phasing software	SOLVE
Refinement software	CNS

Data quality characteristics

	Overall	Outer shell
Low resolution limit [Å]	46.600 *	2.050
High resolution limit [Å]	2.000	2.000
Rmerge	0.061 *	0.531 *
Total number of observations	275520 *
Number of reflections	59761
<I/σ(I)>	16.8	2.6
Completeness [%]	96.5	90.5
Redundancy	4.6	4.6

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, HANGING DROP	7.5 *	295	Kuhn, P., (2002) Proteins, 49, 142. *

Crystallization Reagents in Literatures

ID	crystal ID	solution	reagent name	concentration (unit)	details
1	1	reservoir	Tris-HCl	100 (mM)	pH8.0
2	1	reservoir	PEG200	49 (%(w/v))	or 100mM HEPES, pH7.5
3	1	reservoir	PEG200	44 (%)