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1HKK

High resoultion crystal structure of human chitinase in complex with allosamidin

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]113
Detector technologyCCD
Collection date2002-04-15
Spacegroup nameP 43 21 2
Unit cell lengths94.858, 94.858, 83.483
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution25.000

*

- 1.850
R-factor0.179
Rwork0.179
R-free0.19200

*

Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1guv
RMSD bond length0.010

*

RMSD bond angle2.000

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.920
High resolution limit [Å]1.8501.850
Rmerge0.0480.314
Total number of observations201273

*

Number of reflections328933050

*

<I/σ(I)>15.95.2
Completeness [%]99.393.8
Redundancy6.14.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

6.525 % PEG 550 MME 0.01 M ZNSO4, 0.1 M MES PH 6.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropallosamidin derivative10 (mM)
21dropprotein8 (mg/ml)
31reservoirPEG550 MME25 (%)
41reservoir0.01 (M)
51reservoirMES0.1 (M)pH6.5

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PDB entries from 2024-05-15

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