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4X1M

Structural basis for mutation-induced destabilization of Profilin 1 in ALS

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU MICROMAX-007 HF
Temperature [K]100
Detector technologyCCD
Collection date2013-03-18
DetectorRIGAKU SATURN 944+
Wavelength(s)1.5418
Spacegroup nameC 1 2 1
Unit cell lengths73.650, 31.712, 60.539
Unit cell angles90.00, 122.03, 90.00
Refinement procedure
Resolution19.282 - 2.170
R-factor0.1973
Rwork0.197
R-free0.21390
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1fik
RMSD bond length0.003
RMSD bond angle0.668
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((phenix.refine: 1.9_1692))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.250
High resolution limit [Å]2.1702.170
Rmerge0.0360.095
Number of reflections6468
<I/σ(I)>8.818.3
Completeness [%]99.5100
Redundancy2.62.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6298PFN1 crystals were grown by hanging drop vapor diffusion after mixing the PFN1 protein with a 1:1 ratio of reservoir solution at 298K for E117G. Reservoir solution for E117G contained 50 mM KH2PO4, 41% (wt/vol) PEG 8,000 and 100 mM MES

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