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6OZ8

Crystal structure of Mtb aspartate decarboxylase in active form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-D
Synchrotron siteAPS
Beamline23-ID-D
Temperature [K]130
Detector technologyPIXEL
Collection date2018-08-09
DetectorDECTRIS PILATUS3 6M
Wavelength(s)1.033
Spacegroup nameP 41 21 2
Unit cell lengths163.040, 163.040, 63.570
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution21.920 - 2.700
R-factor0.20356
Rwork0.201
R-free0.25324
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2c45
RMSD bond length0.010
RMSD bond angle1.413
Data reduction softwarePROTEUM PLUS
Data scaling softwarePROTEUM PLUS
Phasing softwarePHENIX
Refinement softwareREFMAC (5.8.0232)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]21.9202.797
High resolution limit [Å]2.7002.700
Number of reflections240342329
<I/σ(I)>15.72.08
Completeness [%]99.6
Redundancy10.4
CC(1/2)0.9990.774
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.5290MES, HEPES, PEG 3350, Ammonium Chloride

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