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1P0I

Crystal structure of human butyryl cholinesterase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]100
Detector technologyCCD
DetectorADSC QUANTUM 4
Wavelength(s)0.933
Spacegroup nameI 4 2 2
Unit cell lengths154.660, 154.660, 127.890
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution55.000

*

- 2.000
R-factor0.195
Rwork0.195
R-free0.22500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ace
RMSD bond length0.014
RMSD bond angle23.700

*

Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareCNS (0.9)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]55.000

*

2.110
High resolution limit [Å]2.0002.000
Rmerge0.074

*

0.448

*

Number of reflections51326

*

<I/σ(I)>6.81.7
Completeness [%]98.699.6
Redundancy7.36.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.520

*

Nachon, F., (2002) Eur.J.Biochem., 269, 630.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein6.6 (mg/ml)
21dropMES0.1 (M)pH6.5
31reservoirammonium sulfate2.05-2.15 (M)

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PDB entries from 2024-10-30

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