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1C4K

ORNITHINE DECARBOXYLASE MUTANT (GLY121TYR)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]295
Detector technologyIMAGE PLATE
DetectorRIGAKU RAXIS IV
Spacegroup nameP 32 2 1
Unit cell lengths111.800, 111.800, 135.900
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution7.000 - 2.700
R-factor0.212
Rwork0.212
R-free0.28100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ord MOLECULE A.
RMSD bond length0.013
RMSD bond angle1.600

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Data reduction softwareDENZO (PACKAGE)
Data scaling softwareSCALEPACK (PACKAGE)
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.800
High resolution limit [Å]2.7002.700
Rmerge0.069

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0.358

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Number of reflections26013
<I/σ(I)>17.5
Completeness [%]94.395.1
Redundancy2.82.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, sitting drop

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6.5

*

293

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20 DEG, SITTING DROP, MICROBRIDGES, RESERVOIRS CONTAINING 30% PEG3350, 0.2 M AMMONIUM ACETATE, AND 0.1 M SODIUM HEPES PH 7.0. DROPS CONSISTED OF EQUAL VOLUMES RESERVOIR AND 20 MG/ML PROTEIN SOLUTION.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20 (mg/ml)
21dropsodium citrate-HCl100 (mM)
31dropdithiothreitol1.0 (mM)
41dropPLP0.2 (mM)
51dropsodium azide0.02 (%)
61dropEDTA0.5 (mM)
71reservoirPEG335030 (%)
81reservoirammonium acetate200 (mM)
91reservoirNa HEPES100 (mM)

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PDB entries from 2024-05-15

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