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1UT6

Structure of acetylcholinesterase (E.C. 3.1.1.7) complexed with N-9-(1',2',3',4'-Tetrahydroacridinyl)-1,8- diaminooctane at 2.4 angstroms resolution.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RUH3R
Temperature [K]120
Detector technologyIMAGE PLATE
Collection date2001-01-18
DetectorRIGAKU IMAGE PLATE
Spacegroup nameP 31 2 1
Unit cell lengths111.193, 111.193, 136.853
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution29.140 - 2.400
R-factor0.194
Rwork0.194
R-free0.24000
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ace
RMSD bond length0.015
RMSD bond angle1.700
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.490
High resolution limit [Å]2.4002.400
Rmerge0.0530.397
Number of reflections38785
<I/σ(I)>16.92.44
Completeness [%]97.097.5
Redundancy3.229.95
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
15.8277PROTEIN WAS CRYSTALLISED FROM 28-33% V/V PEG 200 0.5M MES PH 5.8 AT 4 DEG. CELSIUS; THEN SOAKED IN MOTHER LIQUOR (40% V/V PEG 200 IN 0.1 M MES BUFFER, PH 5.8) CONTAINING 2MM N-9-(1',2',3',4'-TETRAHYDROACRIDINYL) -1,8-DIAMINOOCTANE BIS-HYDROCHLORIDE (A8NH2.2HCL)

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