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- SASDAH6: WbdD(1-459) (bifunctional kinase- methyltransferase WbdD, WbdD) -

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Basic information

Entry
Database: SASBDB / ID: SASDAH6
SampleWbdD(1-459)
  • bifunctional kinase- methyltransferase WbdD (protein), WbdDWorld Blood Donor Day, Escherichia coli
Biological speciesEscherichia coli (E. coli)
CitationJournal: Nat Struct Mol Biol / Year: 2015
Title: A coiled-coil domain acts as a molecular ruler to regulate O-antigen chain length in lipopolysaccharide.
Authors: Gregor Hagelueken / Bradley R Clarke / Hexian Huang / Anne Tuukkanen / Iulia Danciu / Dmitri I Svergun / Rohanah Hussain / Huanting Liu / Chris Whitfield / James H Naismith /
Abstract: Long-chain bacterial polysaccharides have important roles in pathogenicity. In Escherichia coli O9a, a model for ABC transporter-dependent polysaccharide assembly, a large extracellular carbohydrate ...Long-chain bacterial polysaccharides have important roles in pathogenicity. In Escherichia coli O9a, a model for ABC transporter-dependent polysaccharide assembly, a large extracellular carbohydrate with a narrow size distribution is polymerized from monosaccharides by a complex of two proteins, WbdA (polymerase) and WbdD (terminating protein). Combining crystallography and small-angle X-ray scattering, we found that the C-terminal domain of WbdD contains an extended coiled-coil that physically separates WbdA from the catalytic domain of WbdD. The effects of insertions and deletions in the coiled-coil region were analyzed in vivo, revealing that polymer size is controlled by varying the length of the coiled-coil domain. Thus, the coiled-coil domain of WbdD functions as a molecular ruler that, along with WbdA:WbdD stoichiometry, controls the chain length of a model bacterial polysaccharide.
Contact author
  • Anne Tuukkanen (EMBL-Hamburg, European Molecular Biology Laboratory (EMBL) - Hamburg outstation, Notkestraße 85, Geb. 25A, 22607 Hamburg, Deutschland, Germany)

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Models

Model #189
Type: mix / Software: CORAL / Radius of dummy atoms: 1.90 A
Search similar-shape structures of this assembly by Omokage search (details)
Model #192
Type: dummy / Software: DAMMIN / Radius of dummy atoms: 1.90 A
Search similar-shape structures of this assembly by Omokage search (details)

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Sample

SampleName: WbdD(1-459) / Contrast: 3.047 / Dry vol: 59200 / Specimen concentration: 1.00-10.00 / Concentration method: Nanodrop
BufferName: BisTris / Concentration: 20.00 mM / pH: 7 / Composition: 50 mM NaCl, 5 mM DTT
Entity #126Name: WbdDWorld Blood Donor Day / Type: protein / Description: bifunctional kinase- methyltransferase WbdD / Formula weight: 59.2 / Num. of mol.: 1 / Source: Escherichia coli

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Experimental information

BeamInstrument name: DORIS III X33 / City: Hamburg / : Germany / Shape: 0.6 / Type of source: X-ray synchrotronSynchrotron / Wavelength: 0.15 Å / Dist. spec. to detc.: 2.7 mm
DetectorName: Pilatus 1M-W / Pixsize x: 0.172 mm
Scan
Title: WbdD(1-459) / Measurement date: Sep 23, 2011 / Storage temperature: 20 °C / Cell temperature: 20 °C / Exposure time: 15 sec. / Number of frames: 10 / Unit: 1/nm /
MinMax
Q0.0855 6.0292
Distance distribution function P(R)
Sofotware P(R): GNOM 4.5a / Number of points: 435 /
MinMax
Q0.1828 2.563
P(R) point36 470
R0 9.979
Result
D max: 10 / Type of curve: merged / Standard: BSA /
ExperimentalStandardPorod
MW52 kDa52 kDa53 kDa
Volume--90 nm3

P(R)Guinier
Forward scattering, I047.5 47.4
Radius of gyration, Rg3.2 nm3.1 nm

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