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7RT9

Crystal structures of human PYY and NPY

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyCCD
Collection date2015-12-01
DetectorADSC QUANTUM 315r
Wavelength(s)0.9537
Spacegroup nameP 21 21 21
Unit cell lengths76.980, 103.300, 138.350
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution42.110 - 1.900
R-factor0.1809
Rwork0.179
R-free0.21250
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)generic Fab
RMSD bond length0.011
RMSD bond angle1.657
Data reduction softwareMOSFLM
Data scaling softwareAimless (0.5.17)
Phasing softwarePHASER (2.5.7)
Refinement softwareREFMAC (5.8.0258)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]42.11042.1101.930
High resolution limit [Å]1.90010.2301.900
Rmerge0.1200.0400.500
Rmeas0.1300.0440.548
Rpim0.0500.0160.218
Total number of observations571023418424938
Number of reflections871346534337
<I/σ(I)>8.8172.2
Completeness [%]99.698.398.3
Redundancy6.66.45.8
CC(1/2)0.9960.9990.862
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION6.65293Fab-PYY (~5.5 mg/mL with respect to Fab, 2.4:1 molar ratio of PYY:Fab, in 25 mM Tris (pH 7.5), 100 mM NaCl) was mixed with an equal volume (2 uL) of well solution comprising 200 mM citrate (pH 6.65) and 13% (w/v) PEG1500.

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