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1QIP

HUMAN GLYOXALASE I COMPLEXED WITH S-P-NITROBENZYLOXYCARBONYLGLUTATHIONE

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 date1996-07-08
DetectorMARRESEARCH
Spacegroup nameP 43
Unit cell lengths67.300, 67.300, 167.700
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 1.720
R-factor0.17
Rwork0.180
R-free0.21000
Structure solution methodOTHER
RMSD bond length0.010
RMSD bond angle0.023
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]28.0001.750
High resolution limit [Å]1.7201.720
Rmerge0.0480.291
Total number of observations311697

*

Number of reflections78648
<I/σ(I)>164.1
Completeness [%]99.9100
Redundancy43.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

5.815

*

Cameron, A.D., (1997) EMBO J., 16, 3386.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropPEG200012.5-15 (%(w/v))
21dropMES25 (mM)
31drop0.05 (M)
41dropprotein6 (mg/ml)
51drop2-mercaptoethanol0.5 (%)
61dropS-benzyl-glutathione1 (mM)
71reservoirPEG200025-30 (%(w/v))
81reservoirMES50 (mM)
91reservoir0.1 (M)

222036

PDB entries from 2024-07-03

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