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3P5M

Crystal structure of an enoyl-CoA hydratase/isomerase from Mycobacterium avium

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU FR-E+ SUPERBRIGHT
Temperature [K]100
Detector technologyCCD
Collection date2010-08-23
DetectorRIGAKU SATURN 944+
Wavelength(s)1.5418
Spacegroup nameP 21 21 21
Unit cell lengths102.730, 105.180, 130.980
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 2.050
R-factor0.1797
Rwork0.177
R-free0.23410
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3gow
RMSD bond length0.016
RMSD bond angle1.505
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER (2.1.4)
Refinement softwareREFMAC
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]50.0002.100
High resolution limit [Å]2.0509.1702.050
Rmerge0.1070.0210.414
Number of reflections858948955596
<I/σ(I)>11.2549.73.1
Completeness [%]95.97985.3
Redundancy3.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.528919.25 mg/mL protein, 0.2 M K/Na Tartrate, 20% PEG 3350 with 25% ethylene glycol as cryo-protectant, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 289K

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