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6T2D

Multicomponent Peptide Stapling as a Diversity-Driven Tool for the Development of Inhibitors of Protein-Protein Interactions

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, DESY BEAMLINE P11
Synchrotron sitePETRA III, DESY
BeamlineP11
Temperature [K]100
Detector technologyPIXEL
Collection date2018-04-08
DetectorDECTRIS PILATUS 6M-F
Wavelength(s)1.0332
Spacegroup nameP 31 2 1
Unit cell lengths41.017, 41.017, 104.995
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution35.520 - 1.800
R-factor0.1364
Rwork0.132
R-free0.22570
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1rv1
RMSD bond length0.025
RMSD bond angle1.993
Data reduction softwareXDS
Data scaling softwareAimless (0.6.3)
Phasing softwarePHASER
Refinement softwareREFMAC (refmac_5.8.0230)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]35.52035.5201.680
High resolution limit [Å]1.6509.0501.650
Rmerge0.0680.0460.803
Rmeas0.0730.0490.860
Rpim0.0240.0170.302
Total number of observations114541
Number of reflections12894107580
<I/σ(I)>18.1
Completeness [%]99.798.895.3
Redundancy8.97.17.4
CC(1/2)0.9990.9980.899
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP82950.1M TRIS pH 8, 0.2M Ammonium Sulfate, 30% PEG-3350

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PDB entries from 2024-12-25

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