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1QH3

HUMAN GLYOXALASE II WITH CACODYLATE AND ACETATE IONS PRESENT IN THE ACTIVE SITE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X11
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX11
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-11-01
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths39.080, 72.370, 162.060
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution15.000 - 1.900
R-factor0.185
Rwork0.184
R-free0.23900
Structure solution methodSIRAS
RMSD bond length0.007
RMSD bond angle0.023
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]15.0001.930
High resolution limit [Å]1.9001.900
Rmerge0.0630.312

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Total number of observations126060

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Number of reflections36838

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<I/σ(I)>144
Completeness [%]99.099
Redundancy3.42.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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7.1

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EQUILABRATION AGAINST 15-30% W/V PEG 2000 MONOMETHYL ETHER 0.2M MG-ACETATE, 0.1M NA-CACODYLATE PH 6.5 AND 2MM DTT
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirmPEG200015-30 (%(w/v))
21reservoirmagnesium acetate0.2 (M)
31reservoirsodium cacodylate0.1 (M)
41reservoirdithiothreitol2 (mM)
51dropprotain10 (mg/ml)
61dropMOPS10 (mM)
71drop10 (mM)
81dropPEG40025 (%)

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