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1E6V

Methyl-coenzyme M reductase from Methanopyrus kandleri

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]100
Detector technologyIMAGE PLATE
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths80.519, 115.740, 268.510
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.700
R-factor0.239
Rwork0.239
R-free0.27800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1mro
RMSD bond length0.005
RMSD bond angle24.800

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS (0.3)
Refinement softwareCNS (0.3)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.620
High resolution limit [Å]1.6001.600
Rmerge0.0590.259
Number of reflections326507
<I/σ(I)>16.25.3
Completeness [%]93.592.3
Redundancy2.72.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

714

*

pH 7.00
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein30 (mg/ml)
21dropTris-HCl10 (mM)
31reservoirmPEG500010 (%(w/v))
41reservoir2-propanol10 (%(w/v))
51reservoirammonium acetate0.2 (M)
61reservoirmagnesium acetate0.1 (M)
71reservoirglycerol20 (%(w/v))
81reservoirMES/KOH0.1 (M)

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PDB entries from 2024-12-25

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