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2RBI

STRUCTURE OF BINASE MUTANT HIS 101 ASN

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]291
Detector technologyIMAGE PLATE
Collection date1993-10-22
DetectorRIGAKU
Spacegroup nameP 21 21 21
Unit cell lengths111.260, 69.150, 33.370
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 2.200
R-factor0.178

*

Rwork0.178
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)WILD-TYPE BINASE
RMSD bond length0.015
RMSD bond angle0.039
Data reduction softwareDENZO
Data scaling softwareCCP4 ((AGROVATA)
Phasing softwareCCP4
Refinement softwarePROLSQ
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.260
High resolution limit [Å]2.2002.200
Rmerge0.0550.196
Total number of observations51822

*

Number of reflections13288
<I/σ(I)>7.53.8
Completeness [%]97.280.7
Redundancy3.92.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.5291VAPOR DIFFUSION METHOD, WITH 12MG/ML BINASE HIS101ASN, 40MM GLYCINE PH 7.5, 8.75% POLYETHYL- ENE GLYCOL MR 10,000 AND 2.5% SATURATED SODIUM CITRATE IN THE HANGING DROP, AND 17.5% PEG 10,000, 60MM GLYCINE PH 7.5 AND 5% SODIUM CITRATE IN WELL. LEFT FOR 2 DAYS AT 18 DEGREES CENTIGRADE., vapor diffusion, temperature 291K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropbinase H101N12 (mg/ml)
21dropglycine40 (mM)
31dropPEG1000017.5 (%)
41dropsodium citrate2.5 (%sat)
51reservoirPEG1000017.5 (%)
61reservoirglycine60 (mM)
71reservoirsodium citrate5 (%)

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