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2CEK

Conformational Flexibility in the Peripheral Site of Torpedo californica Acetylcholinesterase Revealed by the Complex Structure with a Bifunctional Inhibitor

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]100
Detector technologyCCD
Collection date2005-02-10
DetectorADSC QUANTUM 4
Spacegroup nameP 31 2 1
Unit cell lengths111.940, 111.940, 137.120
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000 - 2.200
R-factor0.175
Rwork0.175
R-free0.20600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ea5
RMSD bond length0.006
RMSD bond angle1.300
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareCNS
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.330
High resolution limit [Å]2.2002.200
Rmerge0.0600.390
Number of reflections50867
<I/σ(I)>16.183.36
Completeness [%]99.999.9
Redundancy4.924.98
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1627732% PEG200, 150MM MES, PH6.0, 4DEG. C. 12 HOURS OF SOAKING WITH A PUTATIVE ANTI-ALZHEIMER DRUG.

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