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1O8A

Crystal Structure of Human Angiotensin Converting Enzyme (Native).

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX14.1
Synchrotron siteSRS
BeamlinePX14.1
Temperature [K]100
Detector technologyCCD
Collection date2002-02-25
DetectorADSC CCD
Spacegroup nameP 21 21 21
Unit cell lengths56.620, 85.060, 133.790
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution47.140 - 2.000
R-factor0.18
Rwork0.180
R-free0.22080

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1o86
RMSD bond length0.005

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RMSD bond angle1.200

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Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.070
High resolution limit [Å]2.0002.000
Rmerge0.0810.432
Number of reflections42782
<I/σ(I)>22.464.44
Completeness [%]98.895.7
Redundancy7.16.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.716

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PEG4000/SODIUM ACETATE., pH 4.70
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropHEPES10 (mM)
21dropPMSF0.1 (%)
31reservoirPEG400015 (%)
41reservoirsodium acetate trihydrate50 (mM)pH4.7
51reservoir10000 (nM)

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