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3H1O

The Structure of Fluorescent Protein FP480

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.0000
Spacegroup nameI 4
Unit cell lengths98.208, 98.208, 108.058
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.210 - 2.000
Rwork0.175
R-free0.22000
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle0.710
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwarePHENIX
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]30.00030.0002.070
High resolution limit [Å]2.0004.3102.000
Rmerge0.0750.0410.534
Number of reflections34954
<I/σ(I)>16.995
Completeness [%]100.0100100
Redundancy4.24.24
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP3.529380mM citric acid, 20% PEG 3350, pH 3.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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