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7TA9

Crystal Structure of thymidylate synthase from Acinetobacter baumannii

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.1
Synchrotron siteALS
Beamline5.0.1
Temperature [K]100
Detector technologyPIXEL
Collection date2021-05-09
DetectorDECTRIS PILATUS3 6M
Wavelength(s)0.97740
Spacegroup nameP 21 21 21
Unit cell lengths64.940, 73.760, 109.380
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.520 - 1.500
R-factor0.1631
Rwork0.162
R-free0.19120
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3ix6
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareMoRDa
Refinement softwarePHENIX (v4438)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]44.52044.5201.540
High resolution limit [Å]1.5006.7101.500
Rmerge0.0350.0160.560
Rmeas0.0380.0170.609
Total number of observations700365
Number of reflections8350110635496
<I/σ(I)>38.9299.543.91
Completeness [%]98.699.388.9
Redundancy8.3887.8595.692
CC(1/2)1.0001.0000.884
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5290Protein at 34 mg/mL was mixed 1:1 (0.4 uL protein and 0.4 uL precipitant) with 10% w/v PEG 20,000, 20% v/v PEG MME 550, 0.03 M each diethyleneglycol, triethyleneglycol, tetraethyleneglycol, and pentaethyleneglycol, and 0.1 M MES/imidazole pH 6.5 (Morpheus E1). Cryo: Direct. Tray: 320511e1: pin: jjg2-4.

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