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11TS

Crystal structure of apo alpha/beta-hydrolase macrolide esterase EstT from Sphingobacterium faecium (S126A mutant)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-B
Synchrotron siteAPS
Beamline23-ID-B
Temperature [K]100
Detector technologyPIXEL
Collection date2025-07-31
DetectorDECTRIS EIGER X 16M
Wavelength(s)1.03
Spacegroup nameP 21 21 21
Unit cell lengths49.923, 82.320, 392.576
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.440 - 3.190
R-factor0.2663
Rwork0.265
R-free0.29620
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.007
RMSD bond angle1.081
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwarePHENIX ((1.21.2_5419: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.4403.340
High resolution limit [Å]3.1903.190
Rmerge0.132
Number of reflections234614512
<I/σ(I)>82.73
Completeness [%]83.6
Redundancy4.8
CC(1/2)0.9900.694
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP277.15HEPES, PEG 4000

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