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3O90

High resolution crystal structures of Streptococcus pneumoniae nicotinamidase with trapped intermediates provide insights into catalytic mechanism and inhibition by aldehydes

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 24-ID-C
Synchrotron siteAPS
Beamline24-ID-C
Temperature [K]100
Detector technologyCCD
Collection date2008-08-15
DetectorADSC QUANTUM 315
Wavelength(s)0.9795
Spacegroup nameP 1 21 1
Unit cell lengths60.838, 120.875, 63.180
Unit cell angles90.00, 114.31, 90.00
Refinement procedure
Resolution41.700 - 1.940
R-factor0.22025
Rwork0.218
R-free0.26077
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.006
RMSD bond angle0.923
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.950
High resolution limit [Å]1.9401.920
Number of reflections54000
<I/σ(I)>11.32.2
Completeness [%]88.273.7
Redundancy3.42.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.329118-22% PEG 3350, 0.2-0.3M NaCl, 0.2M Sodium Malonate, pH 6.3, VAPOR DIFFUSION, HANGING DROP, temperature 291K

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