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9K2H

Crystal structure of the carboxy-terminal channel-forming domain of Colicin Ib

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSRRC BEAMLINE BL13B1
Synchrotron siteNSRRC
BeamlineBL13B1
Temperature [K]80
Detector technologyCCD
Collection date2021-03-18
DetectorADSC QUANTUM 315r
Wavelength(s)1
Spacegroup nameI 41
Unit cell lengths90.742, 90.742, 113.391
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution28.700 - 3.110
R-factor0.2002
Rwork0.198
R-free0.23070
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.009
RMSD bond angle0.909
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHENIX (1.21.1_5286)
Refinement softwarePHENIX (1.21.1_5286)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]28.7003.210
High resolution limit [Å]3.1103.110
Rmerge0.1090.904
Rmeas0.1160.712
Rpim0.0550.356
Number of reflections83328299
<I/σ(I)>16.32.4
Completeness [%]99.798.7
Redundancy4.82.5
CC(1/2)0.8570.769
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP6.5293.151% Nucleosides mix (2% w/v Cytidine, 2% w/v Inosine, 2% w/v Ribavirin, 2% w/v Thymidine, 2% w/v Uridine) 0.1M Buffer system 1(Imidazole; MES monohydrate (acid)) 30% precipitant mix(40% v/v Glycerol; 20% w/v PEG 4000)

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