5P1O

Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 107

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	BESSY BEAMLINE 14.3
Synchrotron site	BESSY
Beamline	14.3
Temperature [K]	100
Detector technology	CCD
Collection date	2013-01-23
Detector	MAR CCD 165 mm
Wavelength(s)	0.8946
Spacegroup name	P 1 21 1
Unit cell lengths	45.257, 73.078, 52.744
Unit cell angles	90.00, 109.41, 90.00

Refinement procedure

Resolution	42.686 - 1.515
R-factor	0.1458
Rwork	0.144
R-free	0.18130
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	4y5l
RMSD bond length	0.008
RMSD bond angle	1.159
Data reduction software	XDS
Data scaling software	XDS
Phasing software	PHASER (2.5.7)
Refinement software	PHENIX

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	42.686		1.610
High resolution limit [Å]	1.520	4.520	1.520
Rmerge	0.076	0.029	0.592
Rmeas	0.088	0.033	0.700
Total number of observations	198071
Number of reflections	49010	1937	6903
<I/σ(I)>	15.2	42.21	2.53
Completeness [%]	97.3	99.5	85.1
Redundancy	4.041
CC(1/2)	0.998	0.999	0.766

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP	4.6	290	0.1 M ammonium acetate, 0.1 M sodium acetate, 24-30% PEG 4000; crystal obtained by streak-seeding and soaked with 90 mM of fragment 107 with the SMILES code OC(=O)\C=C\C(=O)N1CCCCC1