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2NWN

New Pharmacophore for Serine Protease Inhibition Revealed by Crystal Structure of Human Urokinase-type Plasminogen Activator Complexed with a Cyclic Peptidyl Inhibitor, upain-1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsBRUKER AXS MICROSTAR
Temperature [K]100
Detector technologyCCD
Collection date2005-03-25
DetectorBRUKER SMART 6000
Wavelength(s)1.5418
Spacegroup nameH 3
Unit cell lengths120.481, 120.481, 42.117
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution60.240 - 2.150
R-factor0.218
Rwork0.218
R-free0.26100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1f5k
RMSD bond length0.014
RMSD bond angle2.800
Data reduction softwarePROTEUM PLUS (PLUS)
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]60.2402.280
High resolution limit [Å]2.1502.150
Rmerge0.1230.440
Number of reflections16947
<I/σ(I)>5.831.94
Completeness [%]99.699.8
Redundancy6.896.89
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.52980.05M sodium citrate, 1.95M (NH4)2SO4, 0.05% NaN3, 5% PEG 400, pH 4.50, VAPOR DIFFUSION, SITTING DROP, temperature 298K

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