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1NB0

Crystal Structure of Human Riboflavin Kinase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-BM
Synchrotron siteAPS
Beamline19-BM
Temperature [K]100
Detector technologyCCD
Collection date2002-08-25
DetectorCUSTOM-MADE
Wavelength(s)1.0080
Spacegroup nameP 31 2 1
Unit cell lengths57.096, 57.096, 82.505
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution50.000

*

- 1.700
R-factor0.186
Rwork0.184
R-free0.22000

*

Structure solution methodMAD
RMSD bond length0.015
RMSD bond angle1.610

*

Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareSOLVE
Refinement softwareREFMAC (5.1.27)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.760
High resolution limit [Å]1.7001.700
Rmerge0.036

*

0.200

*

Total number of observations212199

*

Number of reflections16996

*

<I/σ(I)>49.24.3
Completeness [%]95.983.2
Redundancy12.47
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.520

*

NA cadodalyte, Mg acetate, PEG 8000, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein15-17 (mg/ml)
21dropTris-HCl50 (mM)
31drop300 (mM)
41dropdithiothreitol1 (mM)pH7.2-7.4
51reservoirsodium cacodylate100 (mM)pH6.5
61reservoirmagnesium acetate200 (mM)
71reservoirPEG800023 (%)

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