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- PDB-4h7i: Crystal structure of haloalkane dehalogenase LinB L138I mutant fr... -

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Database: PDB / ID: 4h7i
TitleCrystal structure of haloalkane dehalogenase LinB L138I mutant from Sphingobium sp. MI1205
ComponentsHaloalkane dehalogenase
KeywordsHYDROLASE / alpha/beta hydrolase fold
Function / homology
Function and homology information

haloalkane dehalogenase / haloalkane dehalogenase activity / metal ion binding
Similarity search - Function
Haloalkane dehalogenase, subfamily 2 / Epoxide hydrolase-like / alpha/beta hydrolase fold / Alpha/beta hydrolase fold-1 / Alpha/Beta hydrolase fold, catalytic domain / Alpha/Beta hydrolase fold / Rossmann fold / 3-Layer(aba) Sandwich / Alpha Beta
Similarity search - Domain/homology
Haloalkane dehalogenase
Similarity search - Component
Biological speciesSphingobium (unknown)
AuthorsOkai, M. / Ohtsuka, J. / Imai, L.F. / Mase, T. / Moriuchi, R. / Tsuda, M. / Nagata, K. / Nagata, Y. / Tanokura, M.
CitationJournal: J.Bacteriol. / Year: 2013
Title: Crystal Structure and Site-Directed Mutagenesis Analyses of Haloalkane Dehalogenase LinB from Sphingobium sp. Strain MI1205.
Authors: Okai, M. / Ohtsuka, J. / Imai, L.F. / Mase, T. / Moriuchi, R. / Tsuda, M. / Nagata, K. / Nagata, Y. / Tanokura, M.
DepositionSep 20, 2012Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Jun 5, 2013Provider: repository / Type: Initial release

Structure visualization

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Deposited unit
A: Haloalkane dehalogenase
hetero molecules

Theoretical massNumber of molelcules
Total (without water)34,3926

  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Unit cell
Length a, b, c (Å)50.421, 72.289, 73.919
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number18
Space group name H-MP21212
Components on special symmetry positions



#1: Protein Haloalkane dehalogenase /

Mass: 34096.586 Da / Num. of mol.: 1 / Mutation: L138I
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Sphingobium (unknown) / Strain: MI1205 / Gene: linB, dhaA / Production host: Escherichia coli (E. coli) / References: UniProt: A4PEU6
#2: Chemical ChemComp-CA / CALCIUM ION

Mass: 40.078 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Ca
#3: Chemical ChemComp-CL / CHLORIDE ION / Chloride

Mass: 35.453 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Cl
#4: Chemical ChemComp-GOL / GLYCEROL / GLYCERIN / PROPANE-1,2,3-TRIOL / Glycerol

Mass: 92.094 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: C3H8O3
#5: Water ChemComp-HOH / water / Water

Mass: 18.015 Da / Num. of mol.: 206 / Source method: isolated from a natural source / Formula: H2O

Experimental details


ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

Sample preparation

CrystalDensity Matthews: 1.98 Å3/Da / Density % sol: 37.74 %
Crystal growTemperature: 278 K / Method: vapor diffusion, sitting drop / Details: VAPOR DIFFUSION, SITTING DROP, temperature 278K

Data collection

Diffraction sourceSource: SYNCHROTRON / Site: Photon Factory / Beamline: BL-5A / Wavelength: 1 Å
DetectorDate: Jun 25, 2010
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 1 Å / Relative weight: 1
ReflectionResolution: 1.8→20 Å / Num. obs: 25640


HKL-2000data collection
HKL-2000data reduction
HKL-2000data scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: 4H77
Resolution: 1.8→20 Å / Cor.coef. Fo:Fc: 0.954 / Cor.coef. Fo:Fc free: 0.941 / SU B: 2.161 / SU ML: 0.069 / Cross valid method: THROUGHOUT / ESU R: 0.134 / ESU R Free: 0.114 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN USED IF PRESENT IN THE INPUT
RfactorNum. reflection% reflectionSelection details
Rfree0.19255 1305 5.1 %RANDOM
Rwork0.17192 ---
obs0.17297 24304 99.57 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: MASK
Displacement parametersBiso mean: 13.66 Å2
Baniso -1Baniso -2Baniso -3
1--0.73 Å20 Å20 Å2
2---0.25 Å20 Å2
3---0.98 Å2
Refinement stepCycle: LAST / Resolution: 1.8→20 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2332 0 15 206 2553
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0070.0192406
X-RAY DIFFRACTIONr_angle_refined_deg1.231.9573269
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.335293
X-RAY DIFFRACTIONr_dihedral_angle_2_deg31.50122.773119
X-RAY DIFFRACTIONr_dihedral_angle_3_deg13.08315376
X-RAY DIFFRACTIONr_dihedral_angle_4_deg12.2391525
X-RAY DIFFRACTIONr_chiral_restr0.0860.2344
X-RAY DIFFRACTIONr_gen_planes_refined0.0050.0211890
LS refinement shellResolution: 1.8→1.846 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.246 93 -
Rwork0.225 1555 -
obs--96.09 %

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