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1HCJ

Photoproduct of the wild-type Aequorea victoria Green Fluorescent Protein

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-1
Synchrotron siteESRF
BeamlineID14-1
Temperature [K]100
Detector technologyCCD
Collection date2000-09-15
DetectorMARRESEARCH
Spacegroup nameP 1 2 1
Unit cell lengths71.770, 65.670, 110.500
Unit cell angles90.00, 103.88, 90.00
Refinement procedure
Resolution33.150 - 1.800
R-factor0.209

*

Rwork0.209
R-free0.26700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1gfl
RMSD bond length0.018
RMSD bond angle0.039
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareMOLREP
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]33.1501.900
High resolution limit [Å]1.8001.800
Rmerge0.0570.251
Total number of observations519063

*

Number of reflections92677
<I/σ(I)>42.7
Completeness [%]97.696.8
Redundancy1.91.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

7.84

*

CRYSTALS WERE GROWN AT 4C FROM 50 MM MGCL2, 14-17 % PEG3350 AND 50-100 MM TRIS/CL PH 7.8 - 8.6.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein15 (mg/ml)
21dropTris-Cl20 (mM)pH7.8
31drop0.01 (%(w/v))
41reservoir50 (mM)
51reservoirPEG335014-17 (%(w/v))
61reservoirTris-Cl50-100 (mM)pH7.8-8.6

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