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1O77

CRYSTAL STRUCTURE OF THE C713S MUTANT OF THE TIR DOMAIN OF HUMAN TLR2

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 32-ID
Synchrotron siteAPS
Beamline32-ID
Temperature [K]100
Collection date2001-06-15
Spacegroup nameP 65 2 2
Unit cell lengths112.300, 112.300, 362.800
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution20.000 - 3.200
R-factor0.249
Rwork0.249
R-free0.31600

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1fyw
RMSD bond length0.009
RMSD bond angle22.600

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCOMO
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0003.400
High resolution limit [Å]3.2003.310
Rmerge0.0870.399
Total number of observations99505

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Number of reflections23135
<I/σ(I)>1510
Completeness [%]98.999.1
Redundancy53
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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721

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1.4M (NH4)2HPO4, 0.1M MES PH 6.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirMES100 (mM)pH6.5, or HEPES(pH7.5)
21reservoir1.2-1.4 (M)
31reservoirdithiothreitol5 (mM)
41dropprotein10-20 (mg/ml)
51dropMOPS20 (mM)pH7.0
61drop150 (mM)
71dropdithiothreitol2 (mM)

222415

PDB entries from 2024-07-10

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