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5KO2

Mouse pgp 34 linker deleted mutant Hg derivative

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2016-03-27
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.00
Spacegroup nameP 21 21 21
Unit cell lengths98.185, 114.741, 375.431
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution33.536 - 3.300
R-factor0.2444
Rwork0.243
R-free0.28480
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4m1m
RMSD bond length0.005
RMSD bond angle0.664
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwarePHENIX (dev_2443)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]49.10950.0003.380
High resolution limit [Å]3.3008.1303.300
Rmerge0.1480.1040.968
Rmeas0.154
Rpim0.042
Total number of observations1309474
Number of reflections114118
<I/σ(I)>9
Completeness [%]92.297.689.4
Redundancy11.514.18.3
CC(1/2)0.9940.217
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.5277Protein is pre-incubated with p-chloromercury phenylsulfonate to a final concentration of 4 mM of the organo mercury compound. To 10.5 ul of protein/organomercury, 3.5 ul of the precipitant 25 mM HEPES 7.5 pH, 100 mM NaCl, 0.3 mM Cymal -7, 28% PEG400 was added. Reservoir: 50 mM HEPES 7.5pH, 100 mM NaCl and 30% PEG400.

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