8AY9

X-RAY CRYSTAL STRUCTURE OF THE CsPYL1(V112L, T135L,F137I, T153I, V168A)-ABA-HAB1 TERNARY COMPLEX

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	ALBA BEAMLINE XALOC
Synchrotron site	ALBA
Beamline	XALOC
Temperature [K]	100
Detector technology	PIXEL
Collection date	2018-10-31
Detector	DECTRIS PILATUS 6M
Wavelength(s)	0.97926
Spacegroup name	P 21 21 21
Unit cell lengths	42.763, 62.923, 187.010
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	44.280 - 2.281
R-factor	0.2055
Rwork	0.203
R-free	0.25960
Structure solution method	FOURIER SYNTHESIS
Starting model (for MR)	5mn0
RMSD bond length	0.008
RMSD bond angle	0.946
Data reduction software	XDS (2018)
Data scaling software	XDS (2018)
Phasing software	PHENIX (1.19.2-4158)
Refinement software	PHENIX (1.19.2-4158)

Data quality characteristics

	Overall	Outer shell
Low resolution limit [Å]	44.280	2.362
High resolution limit [Å]	2.281	2.281
Rmerge	0.157	0.772
Rmeas	0.168	0.820
Number of reflections	23704	1983
<I/σ(I)>	7.38	1.49
Completeness [%]	95.7	83.74
Redundancy	8.6	1.49
CC(1/2)	0.993	0.913

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	MICROBATCH	6	291	30%PEG3350 0.5M CaCl2 Drop 1:1