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1LG5

Crystal Structure Analysis of the HCA II Mutant T199P in complex with beta-mercaptoethanol

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsENRAF-NONIUS FR591
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date1997-12-01
DetectorMAC Science DIP-2030H
Wavelength(s)1.5418
Spacegroup nameC 1 2 1
Unit cell lengths72.840, 44.803, 76.457
Unit cell angles90.00, 92.51, 90.00
Refinement procedure
Resolution20.000 - 1.750
R-factor0.20648
Rwork0.205
R-free0.22700

*

Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.010
RMSD bond angle1.420
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareREFMAC (5.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.810
High resolution limit [Å]1.7501.750
Rmerge0.0660.360
Total number of observations52605

*

Number of reflections22169
Completeness [%]93.194.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.84

*

PEG 2000 or 3350, Tris-HCl, BME, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG200020-22 (%)or PEG3350
21reservoirTris50 (mM)pH7.8
31reservoirbeta-mercaptoethanol3 (mM)
41dropprotein13 (mg/ml)
51dropTris25 (mM)pH8.0
61dropPEG200013 (%)or PEG3350
71dropTris50 (mM)pH7.8
81dropbeta-mercaptoethanol3 (mM)

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