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1AE9

STRUCTURE OF THE LAMBDA INTEGRASE CATALYTIC CORE

Experimental procedure
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X12C
Synchrotron siteNSLS
BeamlineX12C
Temperature [K]113
Detector technologyIMAGE PLATE
Collection date1996-02-10
DetectorMARRESEARCH
Spacegroup nameH 3
Unit cell lengths107.320, 107.320, 108.710
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution16.000 - 1.900
R-factor0.199
Rwork0.199
R-free0.23200
Structure solution methodMIRAS
RMSD bond length0.007
RMSD bond angle1.131

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.851)
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]16.0001.930
High resolution limit [Å]1.9001.900
Rmerge0.042

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Total number of observations110468

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Number of reflections36385

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<I/σ(I)>12.94
Completeness [%]98.999.5
Redundancy2.82.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

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6.1522

*

PROTEIN WAS CRYSTALLIZED FROM 20% PEG 8000 75 MM NACL 7 MM MGCL2 50 MM MES, PH 6.15 40 MM NACITRATE 1 MM DTT 1 MM SPERMINE
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropc17026 (mg/ml)
21reservoirMES50 (mM)
31reservoir75 (mM)
41reservoir7 (mM)
51reservoirsodium citrate40 (mM)
61reservoirDTT1 (mM)
71reservoirEDTA0.1 (mM)
81reservoirspermine-HCl1 (mM)

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