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1JIA

STRUCTURE OF A BASIC PHOSPHOLIPASE A2 FROM AGKISTRODON HALYS PALLAS AT 2.13A RESOLUTION

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]280
Detector technologyAREA DETECTOR
Collection date1995-05
DetectorSIEMENS-NICOLET X200B
Spacegroup nameP 21 21 21
Unit cell lengths97.130, 103.690, 23.270
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution6.000 - 2.130
R-factor0.152
Rwork0.152
R-free0.25500
Structure solution methodSTRUCTURE REFINEMENT
RMSD bond length0.013
RMSD bond angle23.400

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Data reduction softwareXENGEN
Data scaling softwareXENGEN
Phasing softwareX-PLOR
Refinement softwareX-PLOR
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]40.0002.230
High resolution limit [Å]2.1302.130
Rmerge0.0460.176
Total number of observations29753

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Number of reflections12001
<I/σ(I)>31.24.9
Completeness [%]86.146.28
Redundancy2.51.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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9.5THE PROTEIN SOLUTIONS CONTAINED 10MM CA2+, 0.1M NACL, 5% PEG 4K IN 0.01M CHESS BUFFER (PH 9.5) AND AN ENZYME CONCENTRATION OF 11MG/ML; THE SOLUTION IN RESERVOIR CONTAINED 10% PEG 4K IN SAME BUFFER, ROOM TEMPERATURE OF 17 DEGREES C.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein12 (mg/ml)
21dropCHES0.05 (M)
31drop0.1 (M)
41dropPEG40005 (%(w/v))
51drop10 (mg/ml)
61reservoirCHES0.05 (M)
71reservoir0.2 (M)
81reservoirPEG400010 (%(w/v))
91reservoir20 (mg/ml)

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