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6GGD

p53 cancer mutant Y220C in complex with small-molecule stabilizer PK9324

Experimental procedure
実験手法SINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I02
Synchrotron siteDiamond
BeamlineI02
Temperature [K]100
Detector technologyPIXEL
Collection date2015-09-26
DetectorDECTRIS PILATUS 6M-F
Wavelength(s)0.97949
Spacegroup nameP 21 21 21
格子定数 [Å]64.893, 71.247, 105.056
格子定数 [度]90.00, 90.00, 90.00
精密化法
残基29.529 - 1.400
R因子0.150074214253
Rwork0.149
R-free0.16997
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)2j1x
結合長の平均二乗偏差(RMSD) [Å]0.005
結合角の平均二乗偏差(RMSD) [度]0.777
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwarePHENIX
Refinement softwarePHENIX (1.10.1_2155)
Quality characteristics
 OverallOuter shell
分解能 [Å] (低)29.5301.480
分解能 [Å] (高)1.4001.400
Rmerge_l_obs0.0500.520
独立反射数96032
<I/σ(I)>14.52.9
完全性 [%]99.699.9
冗長性4.74.8
結晶化条件
結晶ID方法pH温度溶液条件
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: Saturated solution of 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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件を2024-04-24に公開中

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