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1M6D

Crystal structure of human cathepsin F

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2002-01-11
DetectorMARRESEARCH
Wavelength(s)1.0
Spacegroup nameP 21 21 2
Unit cell lengths68.250, 103.260, 58.650
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 1.700
R-factor0.198
Rwork0.195
R-free0.22000

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1f2a
RMSD bond length0.005
RMSD bond angle1.340

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNX
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.730
High resolution limit [Å]1.7001.700
Rmerge0.086

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0.431

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Total number of observations591413

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Number of reflections43466
<I/σ(I)>323.5
Completeness [%]93.764.5
Redundancy13.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4

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290magnesium acetate, sodium cacodylate, pEG 8000, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 290K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirmagnesium acetate0.2 (M)
21reservoirsodium cacodylate0.1 (M)pH6.
31reservoirPEG800025 (%(w/v))
41dropcathepsin3 (mg/ml)
51dropsodium acetate50 (mM)pH4.0
61dropEDTA1 (mM)
71drop150 (mM)

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PDB entries from 2024-05-15

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