7NZS

Crystal structure of chimeric carbonic anhydrase VA with 2,3,5,6-tetrafluoro-4-(propylsulfanyl)benzenesulfonamide

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	PETRA III, EMBL c/o DESY BEAMLINE P13 (MX1)
Synchrotron site	PETRA III, EMBL c/o DESY
Beamline	P13 (MX1)
Temperature [K]	100
Detector technology	PIXEL
Collection date	2013-05-21
Detector	DECTRIS PILATUS 6M
Wavelength(s)	0.97630
Spacegroup name	P 1 21 1
Unit cell lengths	42.130, 41.304, 71.250
Unit cell angles	90.00, 104.18, 90.00

Refinement procedure

Resolution	40.850 - 1.500
R-factor	0.1725
Rwork	0.169
R-free	0.20180
Structure solution method	MOLECULAR REPLACEMENT
Starting model (for MR)	4ht0
RMSD bond length	0.011
RMSD bond angle	1.970
Data reduction software	XDS
Data scaling software	SCALA (3.3.20)
Phasing software	MOLREP
Refinement software	REFMAC (5.8.0232)

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	69.078	69.078	1.580
High resolution limit [Å]	1.500	4.740	1.500
Rmerge		0.027	0.234
Rmeas	0.056	0.034	0.276
Rpim	0.021	0.013	0.105
Total number of observations	254707	8259	36997
Number of reflections	38049	1269	5516
<I/σ(I)>	17.5	37.4	6
Completeness [%]	99.4	99.1	99.4
Redundancy	6.7	6.5	6.7

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP		291	Crystallization buffer was 0.1M sodium BICINE, pH 9, 0.2 M ammonium sulfate and 2M sodium malonate pH 7 made from 1M sodium BICINE and 3.4M sodium malonate