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1H17

Pyruvate Formate-Lyase (E.coli) in complex with CoA and the substrate analog oxamate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsELLIOT/ENRAF-NONIUS
Temperature [K]100
Detector technologyIMAGE PLATE
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths54.938, 153.169, 205.909
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution15.000 - 1.750
R-factor0.148
Rwork0.148
R-free0.17300
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3pfl
RMSD bond length0.006
RMSD bond angle21.900

*

Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwareCNS
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]15.0001.800
High resolution limit [Å]1.7501.750
Rmerge0.081

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0.366

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Total number of observations596858

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Number of reflections86622
<I/σ(I)>15.774.83
Completeness [%]98.594
Redundancy6.895.03
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.3pH 7.30
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
101reservoir50 (mM)pH7.5
21dropMOPS/NaOH25 (mM)pH7.3
31dropsodium oxamate50 (mM)or sodium pyruvate
41drop3 (mM)
51dropdithiothreitol1 (mM)
61dropEDTA1 (mM)
71drop3 (mM)
81dropPEG5000 MME13 (%(w/v))
91reservoirPEG5000 MME22 (%(w/v))

219140

PDB entries from 2024-05-01

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