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1CIP

GI-ALPHA-1 SUBUNIT OF GUANINE NUCLEOTIDE-BINDING PROTEIN COMPLEXED WITH A GTP ANALOGUE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE A1
Synchrotron siteCHESS
BeamlineA1
Temperature [K]100
Detector technologyCCD
Collection date1998-06
DetectorADSC QUANTUM 4
Spacegroup nameP 32 2 1
Unit cell lengths80.050, 80.050, 105.550
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution15.000 - 1.500
Rwork0.213
R-free0.23500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1gia
RMSD bond length0.011
RMSD bond angle22.830

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]15.0001.550
High resolution limit [Å]1.5001.500
Rmerge0.0510.140
Number of reflections57771
<I/σ(I)>21.67.5
Completeness [%]90.277.4
Redundancy3.922.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

8

*

PROTEIN BOUND TO GPPNHP WAS CRYSTALLIZED IN 1.8-2.0M (NH4)2SO3, 100MM SODIUM ACETATE, H 6.0, 1MM MGSO4, 1MM GPPNHP, AND 5MM DTT. PRIOR TO DATA COLLECTION CRYSTALS WERE TRANSFERED TO 2.0M LI2SO4, 1MM GPPNHP, 3MM DTT, 1MM MGSO4, 100MM BES, PH 7.0, AND 15% GLYCEROL. CRYSTALS WERE FLASH FROZEN IN LIQUID PROPANE.
1Vapor diffusion

*

8

*

PROTEIN BOUND TO GPPNHP WAS CRYSTALLIZED IN 1.8-2.0M (NH4)2SO3, 100MM SODIUM ACETATE, H 6.0, 1MM MGSO4, 1MM GPPNHP, AND 5MM DTT. PRIOR TO DATA COLLECTION CRYSTALS WERE TRANSFERED TO 2.0M LI2SO4, 1MM GPPNHP, 3MM DTT, 1MM MGSO4, 100MM BES, PH 7.0, AND 15% GLYCEROL. CRYSTALS WERE FLASH FROZEN IN LIQUID PROPANE.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21droppotassium phosphate1.4 (M)
31dropEPPS25 (mM)
41drop1 (mM)
51dropGppNHp
61dropdithiothreitol2.5 (mM)
71dropEDTA10 (mM)
81reservoir100 (mM)
91reservoirpotassium phosphate1.45-1.65 (M)

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PDB entries from 2024-05-15

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