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1L0C

Investigation of the Roles of Catalytic Residues in Serotonin N-Acetyltransferase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X4A
Synchrotron siteNSLS
BeamlineX4A
Temperature [K]100
Detector technologyCCD
Collection date2000-04-13
DetectorADSC QUANTUM 4
Wavelength(s)0.979
Spacegroup nameC 2 2 21
Unit cell lengths53.210, 68.681, 89.422
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.300
R-factor0.1877
Rwork0.193
R-free0.24600

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1kuv
RMSD bond length0.007
RMSD bond angle1.300
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.350
High resolution limit [Å]2.3002.300
Rmerge0.0370.092
Total number of observations75910

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Number of reflections7188
<I/σ(I)>25.214.1
Completeness [%]91.993
Redundancy4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.54

*

Wolf, E., (2002) J. Mol. Biol., 317, 215., used microseeding

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirMES100 (mM)pH6.5
21reservoirPEG200030 (%(w/v))
31reservoirammonium acetate0.2 (M)
41reservoirmagnesium acetate0.1 (M)
51reservoirMPD2.0 (%(v/v))
61reservoirdithiothreitol30 (mM)
71reservoirspermidine20 (mM)
81reservoir0.1 (M)
91dropprotein7 (mg/ml)

220113

PDB entries from 2024-05-22

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