1O29

Crystal structure of Thymidylate Synthase Complementing Protein (TM0449) from Thermotoga maritima with FAD and FdUMP 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	2002-04-22
Detector	ADSC QUANTUM 4r
Spacegroup name	P 21 21 21
Unit cell lengths	54.636, 116.955, 141.926
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	20.000 - 2.000
Rwork	0.194
R-free	0.23200 *
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	1kq4
RMSD bond length	0.006
RMSD bond angle	1.190
Data reduction software	MOSFLM
Data scaling software	SCALA
Phasing software	SOLVE
Refinement software	CNS

Data quality characteristics

	Overall	Outer shell
Low resolution limit [Å]	45.200 *	1.950
High resolution limit [Å]	2.000 *	1.900
Rmerge	0.068 *	0.429 *
Total number of observations	264891 *
Number of reflections	62119 *
<I/σ(I)>	14	1.8
Completeness [%]	99.6 *	98 *
Redundancy	4.2	4.1

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	Vapor diffusion, sitting 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 (%)