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1USN

CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THIADIAZOLE INHIBITOR PNU-142372

Experimental procedure
Source typeROTATING ANODE
Source detailsSIEMENS
Temperature [K]293
Detector technologyAREA DETECTOR
Collection date1995-11-15
DetectorSIEMENS
Spacegroup nameH 3 2
Unit cell lengths72.120, 72.120, 192.060
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution10.000 - 1.800
R-factor0.189
Rwork0.189
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)PROTEIN COMPONENT OF STROMELYSIN-1 MODEL (J. W. BECKER ET AL.; 1SLN)
RMSD bond length0.018
RMSD bond angle0.040
Data reduction softwareXENGEN
Data scaling softwareXENGEN
Phasing softwareX-PLOR
Refinement softwarePROFFT
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.710
High resolution limit [Å]1.6001.610
Rmerge0.075

*

0.239

*

Total number of observations96250

*

Number of reflections20522
<I/σ(I)>10.41.83
Completeness [%]95.049
Redundancy4.69
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7HANGING DROP VAPOR DIFFUSION., pH 7.0, vapor diffusion - hanging drop
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropenzyme14.8 (mg/ml)
101reservoirPEG600020-25 (%)
21dropHEPES10 (mM)
31drop5 (mM)
41drop2 (mM)
51drop0.02 (%)
61dropPNU-14237225 (mg/ml)
71dropPEG400100 (%)
81reservoir0.1 (M)
91reservoirHEPES0.1 (M)

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