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4RWB

Racemic influenza M2-TM crystallized from monoolein lipidic cubic phase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 21-ID-F
Synchrotron siteAPS
Beamline21-ID-F
Temperature [K]100
Detector technologyCCD
Collection date2012-06-14
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.97872
Spacegroup nameP 1 21/c 1
Unit cell lengths40.930, 41.230, 27.930
Unit cell angles90.00, 95.68, 90.00
Refinement procedure
Resolution19.390 - 2.000
R-factor0.2816
Rwork0.281
R-free0.29560
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3lbw
RMSD bond length0.013
RMSD bond angle1.641
Data reduction softwareXPREP (2008/2 for Windows)
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.7.0029)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]19.39019.3902.030
High resolution limit [Å]2.0005.5202.000
Number of reflections6119311164
<I/σ(I)>8.8817.642.27
Completeness [%]96.294.895.9
Redundancy7.146.737.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1monoolein lipidic cubic phase6.5298Peptide combined with monoolein at 15-20% (w/w) by codissolving in trifluoroethanol, LCP generated by mixing vacuum-dried solid components with water at 60:40 lipid:water ratio. 200 nL LCP bolus combined with 1 uL solution containing 0.1 M ADA pH 6.5, 24% MPD in glass sandwich plates. Crystals grew in less than 1 day. , monoolein lipidic cubic phase, temperature 298K

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