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9DJM

T4 Lysozyme K147H/T151H

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS-II BEAMLINE 17-ID-2
Synchrotron siteNSLS-II
Beamline17-ID-2
Temperature [K]100
Detector technologyPIXEL
Collection date2023-04-03
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9794
Spacegroup nameP 32 2 1
Unit cell lengths60.221, 60.221, 96.954
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution28.760 - 1.080
R-factor0.1502
Rwork0.150
R-free0.16670
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.006
RMSD bond angle0.973
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX (1.15.2_3472)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]28.7601.110
High resolution limit [Å]1.0801.080
Number of reflections864755709
<I/σ(I)>19.91.8
Completeness [%]99.089.3
Redundancy9.84.8
CC(1/2)1.0000.777
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.8293Protein: 0.33 mM T4 lysozyme mutant. Precipitant: 2.0 M NaH2PO4/K2HPO4, pH 6.8, 150 mM NaCl, 100 mM 1,6-hexanediol, 3% 2-propanol

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