5P1R

Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 110

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	BESSY BEAMLINE 14.2
Synchrotron site	BESSY
Beamline	14.2
Temperature [K]	100
Detector technology	CCD
Collection date	2013-01-23
Detector	MARMOSAIC 225 mm CCD
Wavelength(s)	0.91841
Spacegroup name	P 1 21 1
Unit cell lengths	45.323, 73.088, 52.769
Unit cell angles	90.00, 109.67, 90.00

Refinement procedure

Resolution	42.678 - 1.329
R-factor	0.1434
Rwork	0.142
R-free	0.16800
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	4y5l
RMSD bond length	0.007
RMSD bond angle	1.169
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]	42.678		1.410
High resolution limit [Å]	1.330	3.970	1.330
Rmerge	0.064	0.024	0.603
Rmeas	0.074	0.027	0.703
Total number of observations	303430
Number of reflections	74028	2857	11686
<I/σ(I)>	15.38	52.79	2.27
Completeness [%]	99.3	99.2	97.1
Redundancy	4.098
CC(1/2)	0.999	0.999	0.715

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 110 with the SMILES code CN\C(SCC1=C(C)ON=C1C)=N/C