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4AC5

Lipidic sponge phase crystal structure of the Bl. viridis reaction centre solved using serial femtosecond crystallography

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeFREE ELECTRON LASER
Source detailsSLAC LCLS BEAMLINE AMO
Synchrotron siteSLAC LCLS
BeamlineAMO
Temperature [K]288
Detector technologyCCD
Collection date2010-06-14
DetectorADSC QUANTUM 315r
Wavelength(s)6.2
Spacegroup nameP 21 21 21
Unit cell lengths57.500, 84.600, 375.800
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution46.100 - 8.200
R-factor0.35239
Rwork0.351
R-free0.38400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2wjn
RMSD bond length0.006
RMSD bond angle1.650
Data reduction softwareCrystFEL (0.1.0 INDEXAMAJIG)
Data scaling softwareMONTE (CARLO INTEGRATION)
Phasing softwarePHASER
Refinement softwareREFMAC (5.5.0102)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]46.1007.620
High resolution limit [Å]7.4007.370
Rmerge0.500
Number of reflections2431
<I/σ(I)>1.9
Completeness [%]85.021.1
Redundancy81.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
17.9BATCH CRYSTALLIZATIONS WERE SET UP IN SEPTUM-SEALED GLASS VIALS CONTAINING 100 UL PROTEIN (20-30 MG/ML) , 100 UL LIPIDIC SPONGE PHASE (12 % MONOOLEIN, 17.5 % JEFFAMINE M- 600, 1.0 M HEPES PH 8.0, 0.7 M (NH4)2SO4, 2.5 % 1,2,3- HEPTANETRIOL) AND 50 UL 1.0-1.2 M TRI-SODIUM CITRATE

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