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2XLN

Crystal structure of a complex between Actinomadura R39 DD-peptidase and a boronate inhibitor

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM30A
Synchrotron siteESRF
BeamlineBM30A
Temperature [K]100
Collection date2010-01-25
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths102.994, 91.258, 106.878
Unit cell angles90.00, 94.46, 90.00
Refinement procedure
Resolution33.350 - 2.400
R-factor0.19423
Rwork0.191
R-free0.24719
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle1.150
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.6002.530
High resolution limit [Å]2.4002.400
Rmerge0.1000.520
Number of reflections77046
<I/σ(I)>18.13.6
Completeness [%]99.699.5
Redundancy76.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1

226707

PDB entries from 2024-10-30

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