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1H9A

COMPLEX OF ACTIVE MUTANT (Q365->C) OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE FROM L. MESENTEROIDES WITH COENZYME NADP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]293
Detector technologyIMAGE PLATE
Collection date1994-11-15
DetectorMARRESEARCH
Spacegroup nameP 62 2 2
Unit cell lengths136.700, 136.700, 121.200
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution21.200 - 2.160
R-factor0.187
Rwork0.187
R-free0.22600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)SUBUNIT 'A' OF 1DPG
RMSD bond length0.006
RMSD bond angle22.530

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.240
High resolution limit [Å]2.1602.160
Rmerge0.138

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0.506

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Total number of observations93186

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Number of reflections328682822

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<I/σ(I)>8.11.8
Completeness [%]90.281.3
Redundancy2.82.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5

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291

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HANGING DROP VAPOUR DIFFUSION, 2+2 MICROLITER DROPS. THE PROTEIN AT 5MG/ML IN 100MM TRIS-HCL AT PH 7.5 WITH 0.5MM NADP+. DROPS EQUILIBRIATED AGAINST 1.7M UNBUFFERED AMMONIUM SULFATE.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein5 (mg/ml)
21dropTris-HCl100 (mM)
31dropNADP+0.500 (mM)
41reservoirammonium sulfate1.64 (M)unbuffered

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PDB entries from 2024-05-15

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