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6GGF

Structure of the p53 cancer mutant Y220C in complex with small-molecule stabilizer PK9328

Experimental procedure
実験手法SINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I03
Synchrotron siteDiamond
BeamlineI03
Temperature [K]100
Detector technologyPIXEL
Collection date2017-08-08
DetectorDECTRIS PILATUS3 6M
Wavelength(s)0.98
Spacegroup nameP 21 21 21
格子定数 [Å]65.110, 71.209, 105.351
格子定数 [度]90.00, 90.00, 90.00
精密化法
残基29.608 - 1.320
R因子0.149570400365
Rwork0.148
R-free0.17082
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]0.818
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwarePHENIX
Refinement softwarePHENIX (1.10.1_2155)
Quality characteristics
 OverallOuter shell
分解能 [Å] (低)29.6101.390
分解能 [Å] (高)1.3201.320
Rmerge_l_obs0.0490.550
独立反射数114821
<I/σ(I)>163.3
完全性 [%]99.599.3
冗長性5.14.8
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 NaCl, 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 NaCl.

218500

件を2024-04-17に公開中

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