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8TA1

Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor MAM907

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSEALED TUBE
Source detailsBRUKER D8 QUEST
Temperature [K]100
Detector technologyPIXEL
Collection date2023-06-21
DetectorBruker PHOTON III
Wavelength(s)1.5418
Spacegroup nameP 1 21 1
Unit cell lengths28.722, 66.265, 44.138
Unit cell angles90.00, 92.21, 90.00
Refinement procedure
Resolution22.270 - 1.500
R-factor0.1476
Rwork0.146
R-free0.16740
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.010
RMSD bond angle1.105
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX (1.21rc1_4933)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]44.1101.530
High resolution limit [Å]1.5001.500
Rmerge0.1021.247
Rmeas0.1091.378
Rpim0.0370.571
Total number of observations2308967525
Number of reflections265091304
<I/σ(I)>18.11.5
Completeness [%]100.0
Redundancy8.75.8
CC(1/2)0.9980.476
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.6291Berkeley H8: 30% (w/v) PEG 4000, 100 mM Sodium acetate / Hydrochloric acid pH 4.6, 200 mM Ammonium acetate. Plate 13388 H8 drop 1. MyulA.01062.a.B13.PS38720 at 8.9 mg/mL. 2mM MAM907 and 2mM NADP added to the protein prior to crystallization. Plate 13388 well H8 drop 1, Cryo: 80% crystallant + 20% PEG 200

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