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1RP9

Crystal structure of barley alpha-amylase isozyme 1 (amy1) inactive mutant d180a in complex with acarbose

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM30A
Synchrotron siteESRF
BeamlineBM30A
Temperature [K]100
Detector technologyCCD
Collection date2000-12-13
DetectorMARRESEARCH
Wavelength(s)0.9500
Spacegroup nameP 21 21 2
Unit cell lengths93.730, 73.540, 61.060
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution39.520 - 2.000
R-factor0.166
Rwork0.166
R-free0.22600
Structure solution methodFOURIER DIFFERENCE
Starting model (for MR)1ht6
RMSD bond length0.013
RMSD bond angle1.600
Data reduction softwareMOSFLM
Data scaling softwareCCP4 ((SCALA))
Phasing softwareCNS
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.5202.050
High resolution limit [Å]2.0002.000
Number of reflections25774
<I/σ(I)>7.52.4
Completeness [%]100.0100
Redundancy4.44.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.7290PEG 8000, ISOPROPANOL, pH 6.7, VAPOR DIFFUSION, HANGING DROP, temperature 290K

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