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1AX9

ACETYLCHOLINESTERASE COMPLEXED WITH EDROPHONIUM, LAUE DATA

Experimental procedure
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID09
Synchrotron siteESRF
BeamlineID09
Temperature [K]273
Detector technologyCCD
Collection date1995-04-30
Spacegroup nameP 31 2 1
Unit cell lengths113.000, 113.000, 136.900
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000 - 2.800
R-factor0.207
R-free0.26800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ace
Data reduction softwareLaueView
Data scaling softwareLaueView
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.2003.000
High resolution limit [Å]2.8002.800
Rmerge0.148

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Total number of observations83171

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Number of reflections21492
Completeness [%]84.561.3
Redundancy4.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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5.84

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Raves, M.L., (1997) Nature Struct.Biol., 4, 57.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG20038 (%)
21reservoirMES0.1 (M)
31dropprotein12 (mg/ml)

219869

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