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5O1C

p53 cancer mutant Y220C in complex with compound MB184

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I03
Synchrotron siteDiamond
BeamlineI03
Temperature [K]100
Detector technologyPIXEL
Collection date2014-03-09
DetectorDECTRIS PILATUS3 S 6M
Wavelength(s)0.976250
Spacegroup nameP 21 21 21
Unit cell lengths65.192, 71.119, 105.309
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.469 - 1.320
R-factor0.152
Rwork0.151
R-free0.17180
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)2j1x
RMSD bond length0.005
RMSD bond angle0.816
Refinement softwarePHENIX ((1.10.1_2155: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.5001.390
High resolution limit [Å]1.3201.320
Rmerge0.0560.590
Number of reflections113139
<I/σ(I)>16.23.9
Completeness [%]98.297
Redundancy5.55.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP293Protein solution: 6 mg/ml protein in 25 mM sodium phosphate, ph 7.2, 150 mm KCl, 5 mm DTT. Reservoir buffer: 100 mm HEPES, pH 7.2, 19% (w/v) polyethylene glycol 4000, 5 mm DTT. Soaking buffer: 30 mM compound in 100 mm HEPES, ph 7.2, 10 mM sodium phosphate, ph 7.2, 19% (w/v) polyethylene glycol 4000, 20 % (v/v) glycerol, 150 mm KCl.

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