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4NTD

Crystal structure of HlmI

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X06SA
Synchrotron siteSLS
BeamlineX06SA
Temperature [K]100
Detector technologyPIXEL
Collection date2013-09-13
DetectorPSI PILATUS 6M
Wavelength(s)1.0
Spacegroup nameP 31 2 1
Unit cell lengths96.350, 96.350, 133.490
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution10.000 - 1.600
R-factor0.1471
Rwork0.146
R-free0.15938
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4fk1
RMSD bond length0.006
RMSD bond angle1.259
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHASER
Refinement softwareREFMAC (5.7.0029)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.700
High resolution limit [Å]1.6001.600
Rmerge0.0560.498
Number of reflections93867
<I/σ(I)>11.22.2
Completeness [%]98.999.9
Redundancy3.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.32931.3M Na/K phosphate, pH 7.3, VAPOR DIFFUSION, SITTING DROP, temperature 293K

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