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1B8Y

X-RAY STRUCTURE OF HUMAN STROMELYSIN CATALYTIC DOMAIN COMPLEXED WITH NON-PEPTIDE INHIBITORS: IMPLICATIONS FOR INHIBITOR SELECTIVITY

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]293
Detector technologyIMAGE PLATE
Collection date1995-06-15
DetectorMARRESEARCH
Spacegroup nameP 41 21 2
Unit cell lengths69.970, 69.970, 77.670
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.000
R-factor0.197

*

Rwork0.197
R-free0.21400
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.011
RMSD bond angle2.600
Data reduction softwareXDS
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.0002.100
High resolution limit [Å]2.0002.000
Rmerge0.091

*

0.340

*

Total number of observations142019

*

Number of reflections13572
Completeness [%]99.999.9
Redundancy10.59.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

6.5pH 6.5, VAPOR DIFFUSION, HANGING DROP
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111PEG 8000
211SODIUM CACODYLATE
311(NH4)2SO4
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein-inhibitor complex0.5-1 (mM)
21dropPEG800010-15 (%)
31dropammonium sulfate0.05 (M)
41dropsodium cacodylate0.05 (M)
51reservoirPEG800020-30 (%)
61reservoirammonium sulfate0.1 (M)
71reservoirsodium cacodylate0.1 (M)

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