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6Z3N

Apo Structure of a Hydrolase from Pseudomonas aeruginosa PAO1

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]100
Detector technologyPIXEL
Collection date2019-12-14
DetectorDECTRIS EIGER2 XE 16M
Wavelength(s)0.9795
Spacegroup nameC 1 2 1
Unit cell lengths85.310, 85.900, 122.640
Unit cell angles90.00, 102.34, 90.00
Refinement procedure
Resolution59.900 - 1.580
Rwork0.137
R-free0.20040
Structure solution methodSAD
RMSD bond length0.012
RMSD bond angle1.676
Data reduction softwarexia2
Data scaling softwareAimless
Phasing softwareCRANK2
Refinement softwareREFMAC (5.8.0258)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]59.9001.610
High resolution limit [Å]1.5801.580
Number of reflections959451474
<I/σ(I)>23.2
Completeness [%]81.3
Redundancy5.9
CC(1/2)0.9990.573
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP29312 mg/mL of PaSpo2 protein stock in the buffer of 25 mM Tris pH 8.0, 200 mM NaCl, and 10 mM MgCl2 is mixed 1:1 ratio with the precipitant consisted of 4.0 M NH4OAc, 0.1 M Bis-Tris propane, pH 7.0

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