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- PDB-4amq: A Megaviridae Orfan gene encodes a new nucleotidyl transferase -

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Basic information

Entry
Database: PDB / ID: 4amq
TitleA Megaviridae Orfan gene encodes a new nucleotidyl transferase
ComponentsL544
KeywordsTRANSFERASE / MIMIVIRUS / MG662 / TRANSCRIPTION COUPLED DNA REPAIR
Function / homologyvirion component => GO:0044423 / : / Uncharacterized protein L544
Function and homology information
Biological speciesACANTHAMOEBA POLYPHAGA MIMIVIRUS
MethodX-RAY DIFFRACTION / SYNCHROTRON / MAD / Resolution: 2.17 Å
AuthorsLartigue, A. / Claverie, J.M. / Priet, S. / Abergel, C.
Citation
Journal: To be Published
Title: A Megaviridae Orphan Gene Encodes a New Nucleotidyl Transferase
Authors: Ciaccafava, A. / Lartigue, A. / Mansuelle, P. / Jeudy, S. / Abergel, C.
#1: Journal: Acta Crystallogr.,Sect.F / Year: 2011
Title: Preliminary Crystallographic Analysis of a Possible Transcription Factor Encoded by the Mimivirus L544 Gene.
Authors: Ciaccafava, A. / Lartigue, A. / Mansuelle, P. / Jeudy, S. / Abergel, C.
History
DepositionMar 13, 2012Deposition site: PDBE / Processing site: PDBE
Revision 1.0Mar 20, 2013Provider: repository / Type: Initial release

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: L544
hetero molecules


Theoretical massNumber of molelcules
Total (without water)48,4694
Polymers48,3351
Non-polymers1343
Water2,198122
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)60.445, 91.092, 152.994
Angle α, β, γ (deg.)90.00, 90.00, 90.00
Int Tables number20
Space group name H-MC2221
Components on special symmetry positions
IDModelComponents
11A-2016-

HOH

21A-2090-

HOH

31A-2098-

HOH

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Components

#1: Protein L544


Mass: 48334.707 Da / Num. of mol.: 1
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) ACANTHAMOEBA POLYPHAGA MIMIVIRUS / Plasmid: PDEST17 / Production host: ESCHERICHIA COLI (E. coli) / Strain (production host): BL21(DE3) / Variant (production host): ROSETTA / References: UniProt: Q5UQA5
#2: Chemical ChemComp-MN / MANGANESE (II) ION


Mass: 54.938 Da / Num. of mol.: 2 / Source method: obtained synthetically / Formula: Mn
#3: Chemical ChemComp-MG / MAGNESIUM ION


Mass: 24.305 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: Mg
#4: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 122 / Source method: isolated from a natural source / Formula: H2O
Nonpolymer detailsMANGANESE (II) ION (MN): LOCATED IN THE NUCLEOTIDYL TRANSFERASE CATALYTIC DOMAIN
Sequence detailsADDITIONAL N-TERMINAL HIS-TAG, LEU -1 REPLACES INITIATION METHIONINE. NUCLEOTIDYL TRANSFERASE ...ADDITIONAL N-TERMINAL HIS-TAG, LEU -1 REPLACES INITIATION METHIONINE. NUCLEOTIDYL TRANSFERASE CATALYTIC DOMAIN IS RESIDUES 1-197.

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Experimental details

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Experiment

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

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Sample preparation

CrystalDensity Matthews: 2.18 Å3/Da / Density % sol: 43.58 %
Crystal growpH: 6
Details: PROTEIN CONCENTRATION: 10 MG/ML IN 10 MM CHES BUFFER PH 9.0 RESERVOIR: 4 TO 12% PEG 4000, 0.1 M SODIUM CACODYLATE BETWEEN PH 6 AND 7, 0.1 M MNCL2

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Data collection

DiffractionMean temperature: 105 K
Diffraction sourceSource: SYNCHROTRON / Site: ESRF / Beamline: ID23-1 / Wavelength: 0.97918
DetectorType: ADSC CCD / Detector: CCD / Date: Nov 7, 2010
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97918 Å / Relative weight: 1
ReflectionResolution: 2.17→50.4 Å / Num. obs: 20963 / % possible obs: 96 % / Redundancy: 2.8 % / Biso Wilson estimate: 34.3 Å2 / Rmerge(I) obs: 0.08 / Net I/σ(I): 3.8
Reflection shellResolution: 2.17→2.25 Å / Redundancy: 2.7 % / Rmerge(I) obs: 0.36 / Mean I/σ(I) obs: 1.9 / % possible all: 96

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Processing

Software
NameVersionClassification
PHENIX(PHENIX.REFINE)refinement
MOSFLMdata reduction
SCALAdata scaling
autoSHARPphasing
RefinementMethod to determine structure: MAD
Starting model: NONE

Resolution: 2.17→29.29 Å / SU ML: 0.31 / σ(F): 0.03 / Phase error: 25.6 / Stereochemistry target values: ML
Details: - LOOP RESIDUES 120 TO 126 ARE DISORDERED - LINKER RESIDUES 198 TO 210 ARE DISORDERED - RESIDUES 360 TO THE END ARE DISORDERED
RfactorNum. reflection% reflection
Rfree0.2442 1088 5.2 %
Rwork0.2192 --
obs0.2206 20963 92.15 %
Solvent computationShrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL / Bsol: 50.034 Å2 / ksol: 0.363 e/Å3
Displacement parametersBiso mean: 46.6 Å2
Baniso -1Baniso -2Baniso -3
1-8.3615 Å20 Å20 Å2
2--1.4128 Å20 Å2
3----9.7743 Å2
Refinement stepCycle: LAST / Resolution: 2.17→29.29 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms2870 0 3 122 2995
Refine LS restraints
Refine-IDTypeDev idealNumber
X-RAY DIFFRACTIONf_bond_d0.0032926
X-RAY DIFFRACTIONf_angle_d0.6783949
X-RAY DIFFRACTIONf_dihedral_angle_d12.5631122
X-RAY DIFFRACTIONf_chiral_restr0.048448
X-RAY DIFFRACTIONf_plane_restr0.004489
LS refinement shell
Resolution (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
2.1701-2.26880.29661340.24572371X-RAY DIFFRACTION89
2.2688-2.38840.27161240.24632394X-RAY DIFFRACTION90
2.3884-2.53790.28471340.23542475X-RAY DIFFRACTION93
2.5379-2.73380.32921390.23242529X-RAY DIFFRACTION94
2.7338-3.00860.26591410.24442494X-RAY DIFFRACTION94
3.0086-3.44340.26811480.22392538X-RAY DIFFRACTION94
3.4434-4.33610.21071310.19352535X-RAY DIFFRACTION93
4.3361-29.29290.2031370.20232539X-RAY DIFFRACTION90

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