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6S1V

Crystal structure of dimeric M-PMV protease D26N mutant in complex with inhibitor

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyPIXEL
Collection date2013-03-28
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.91841
Spacegroup nameP 1 21 1
Unit cell lengths49.947, 29.504, 85.390
Unit cell angles90.00, 101.71, 90.00
Refinement procedure
Resolution48.910 - 1.640
R-factor0.18006
Rwork0.179
R-free0.22018
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6s1u chain A
RMSD bond length0.015
RMSD bond angle1.701
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0232)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]48.9101.740
High resolution limit [Å]1.6401.640
Rmerge0.0430.826
Rmeas0.0500.970
Number of reflections304084819
<I/σ(I)>14.361.37
Completeness [%]99.398.3
Redundancy3.653.56
CC(1/2)0.9990.568
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.6292Protein solution: 5.0 mg/mL protein with 1.4-fold molar excess (relative to dimeric protein) of Pro-0A1-Val-PSA-Ala-Met-Thr (inhibitor), 5 mM TCEP, 10 mM Tris buffer pH 7.4; Reservoir solution: 0.1 M sodium citrate buffer, 25% propan-2-ol, 5 mM TCEP;

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