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1AKN

STRUCTURE OF BILE-SALT ACTIVATED LIPASE

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]288
Detector technologyIMAGE PLATE
Collection date1996-12
DetectorRIGAKU RAXIS II
Spacegroup nameP 31 2 1
Unit cell lengths94.390, 94.390, 144.510
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution8.000 - 2.800
R-factor0.216

*

Rwork0.211
R-free0.28300

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ACE
RMSD bond length0.008
RMSD bond angle23.800

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]34.000

*

2.900
High resolution limit [Å]2.8002.800
Rmerge0.0660.391

*

Number of reflections18614
<I/σ(I)>13.82.8
Completeness [%]98.499.8

*

Redundancy2.531.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

720

*

pH 7.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein12.5 (mg/ml)
21dropammonium sulfate0.9 (M)
31dropisopropanol2.5 (%)
41dropzwittergent 3-120.5 (mM)
51reservoirammonium sulfate1.8 (M)
61reservoirisopropanol5 (%)
71reservoirzwittergent 3-121 (mM)

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PDB entries from 2024-10-30

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