User:Fadel A. Samatey/FlgE I
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- | There is also close structural similarity between domains D1 and D2 comparing FlgE-Cc32 with FlgE-St42, and comparing | + | There is also close structural similarity between domains D1 and D2 comparing FlgE-Cc32 with FlgE-St42, and comparing FlgE2-Cj79 with FlgE-Cc32 (Supplementary Fig. 3 in the journal article). |
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Revision as of 22:46, 19 October 2016
Interactive 3D Complement in Proteopedia
Scientific Reports an online, open access journal: nature.com/srep
Structural insights into bacterial flagellar hook similarities and specifities.
Young-Ho Yoon, Clive S. Barker, Paula V. Bulieris, Hideyuki Matsunami, and Fadel A. Samatey.
Scientific Reports 6:35552, 2016: nature.com/articles/srep35552. (DOI: 10.1038/srep35552)
The interactive Molecular Tour below assumes that you are familiar with the journal article.
Molecular Tour
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Notes and References
- ↑ Kido Y, Yoon YH, Samatey FA. Crystallization of a 79 kDa fragment of the hook protein FlgE from Campylobacter jejuni. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2011 Dec 1;67(Pt, 12):1653-7. Epub 2011 Nov 30. PMID:22139190 doi:10.1107/S1744309111043272
- ↑ Wagenknecht T, DeRosier D, Shapiro L, Weissborn A. Three-dimensional reconstruction of the flagellar hook from Caulobacter crescentus. J Mol Biol. 1981 Sep 25;151(3):439-65. PMID:7338902 doi:http://dx.doi.org/10.1016/0022-2836(81)90005-X
- ↑ The Caulobacter crecentus hook model contains 55 copies of the monomer, for a total of 121,055 non-hydrogen atoms. There are 16,665 alpha carbon atoms in the model. The van der Waals radius of carbon is 1.7 Å. In order to make the FlgE domains look solid, the alpha carbons are displayed with a radius of 3.5 Å.