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7Q1K

Crystal structure of the native AA9A LPMO from Thermoascus aurantiacus

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, EMBL c/o DESY BEAMLINE P13 (MX1)
Synchrotron sitePETRA III, EMBL c/o DESY
BeamlineP13 (MX1)
Temperature [K]100
Detector technologyPIXEL
Collection date2020-11-30
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.9762
Spacegroup nameP 21 21 21
Unit cell lengths37.690, 64.191, 88.533
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.270 - 1.360
R-factor0.1523
Rwork0.150
R-free0.18520
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2yet
RMSD bond length0.005
RMSD bond angle0.866
Data scaling softwareAimless (0.5.27)
Phasing softwarePHASER
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]44.3601.410
High resolution limit [Å]1.3601.360
Rmeas0.2182.900
Rpim0.0591.203
Number of reflections433592631
<I/σ(I)>9.10.8
Completeness [%]92.658.5
Redundancy12.9
CC(1/2)0.9980.250
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2890.2 M ammonium sulfate, 0.1 M HEPES-NaOH pH 7.5, 25% w/v PEG 3350

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