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1MD7

Monomeric structure of the zymogen of complement protease C1r

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID13
Synchrotron siteESRF
BeamlineID13
Temperature [K]77
Detector technologyCCD
Collection date2000-10-28
DetectorMARRESEARCH
Wavelength(s)0.964
Spacegroup nameP 64
Unit cell lengths167.060, 167.060, 43.648
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution50.000

*

- 3.200
R-factor0.2428
Rwork0.217
R-free0.27860

*

Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.007

*

RMSD bond angle25.000

*

Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.000

*

3.370
High resolution limit [Å]3.2003.200
Rmerge0.120

*

0.360

*

Number of reflections48443

*

<I/σ(I)>51.8
Completeness [%]95.9

*

95.3
Redundancy4.43.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.4

*

293ammonium sulfate, TAPS, pH 8.4, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein8 (mg/ml)
21droptriethanolamine-hydrochloride50 (mM)
31drop145 (mM)pH7.4
41reservoirammonium sulfate1.5 (M)
51reservoirTAPS100 (mM)pH8.4

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