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1E19

Structure of the carbamate kinase-like carbamoyl phosphate synthetase from the hyperthermophilic archaeon Pyrococcus furiosus bound to ADP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF
Synchrotron siteESRF
Temperature [K]100
Detector technologyCCD
Collection date1998-09-15
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths55.400, 91.700, 133.800
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution15.000 - 1.500
R-factor0.183

*

Rwork0.183
R-free0.21800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1b7b
RMSD bond length0.020
RMSD bond angle9.900

*

Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]76.6701.590
High resolution limit [Å]1.4301.500
Rmerge0.0670.355
Total number of observations448640

*

Number of reflections116569
<I/σ(I)>5.21.9
Completeness [%]97.398.6
Redundancy3.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

8.5

*

22

*

1.3M SODIUM CITRATE 0.1M TRIS-HCL, PH=8.5, 0-10% ETHYLENE GLYCOL PROTEIN SOLUTION: 10MG/ML OF PROTEIN IN 10MM TRIS-HCL CONTAINING 20MM ATP AND MGCL2, pH 8.00
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropTris-HCl50 (mM)
21dropATP20 (mM)
31drop20 (mM)
41reservoirsodium citrate1.3 (M)
51reservoirTris-HCl0.1 (M)pH8.5

218853

数据于2024-04-24公开中

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