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6GMI

Genetic Engineering of an Artificial Metalloenzyme for Transfer Hydrogenation of a Self-Immolative Substrate in E. coli's Periplasm.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X06DA
Synchrotron siteSLS
BeamlineX06DA
Temperature [K]100
Detector technologyPIXEL
Collection date2018-05-18
DetectorDECTRIS EIGER X 16M
Wavelength(s)1.000
Spacegroup nameI 41 2 2
Unit cell lengths57.507, 57.507, 184.130
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution46.070 - 1.600
R-factor0.18728
Rwork0.187
R-free0.19940
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2qcb
RMSD bond length0.015
RMSD bond angle2.523
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0222)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]46.0701.630
High resolution limit [Å]1.6001.600
Rmerge0.1174.330
Number of reflections20991
<I/σ(I)>15.6
Completeness [%]100.0
Redundancy25.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP92930.1 M SPG 9 pH (Buffer) 25 %w/v PEG 1500 (Precipitant)

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