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8BRC

Crystal structure of the adduct between human serum transferrin and cisplatin

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsELETTRA BEAMLINE 11.2C
Synchrotron siteELETTRA
Beamline11.2C
Temperature [K]100
Detector technologyPIXEL
Collection date2022-10-29
DetectorDECTRIS PILATUS 6M
Wavelength(s)1.0000
Spacegroup nameC 2 2 21
Unit cell lengths136.340, 156.400, 107.440
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution102.770 - 3.170
R-factor0.1808
Rwork0.177
R-free0.24316
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4x1b
RMSD bond angle0.979
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0352)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]102.7703.220
High resolution limit [Å]3.1703.170
Number of reflections19869969
<I/σ(I)>13.72.3
Completeness [%]100.0100
Redundancy12.813.5
CC(1/2)1.0000.800
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.529315% w/v PEG 3350, 16% v/v glycerol, 8 mM disodium malonate, and 150 mM Na-PIPES pH 6.5

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