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1LQA

TAS PROTEIN FROM ESCHERICHIA COLI IN COMPLEX WITH NADPH

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 17-ID
Synchrotron siteAPS
Beamline17-ID
Temperature [K]100
Detector technologyCCD
Collection date2001-12-08
DetectorADSC QUANTUM 4
Wavelength(s)1.0072
Spacegroup nameP 21 21 21
Unit cell lengths58.300, 81.460, 145.020
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 1.600

*

R-factor0.14634
Rwork0.145
R-free0.18600

*

Structure solution methodMAD
RMSD bond length0.017
RMSD bond angle1.800

*

Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareMLPHARE
Refinement softwareREFMAC (5.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.640
High resolution limit [Å]1.6001.600
Rmerge0.063

*

0.175
Number of reflections160862

*

<I/σ(I)>23.84.1
Completeness [%]92.0

*

57.8
Redundancy3.3

*

3.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.52950.1M Tris, 15% PEG8000, 50mM Ammonium Sulfate, 0.2M Magnesium Chloride, 10mM NADPH, pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirTris0.1 (M)pH8.5
21reservoirPEG800015 (%)
31reservoirammonium sulfate50 (mM)
41reservoir0.2 (M)

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