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Sandbox Reserved 1481

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== References ==
== References ==
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[http://www.rcsb.org/structure/5K7M]
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<Structural basis of N(6)-adenosine methylation by the METTL3-METTL14 complex./>[http://www.rcsb.org/structure/5K7M]
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[https://www.ncbi.nlm.nih.gov/pubmed/27281194]
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<references/>[https://www.ncbi.nlm.nih.gov/pubmed/27281194]
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[https://www.ncbi.nlm.nih.gov/pubmed/27627798]
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<references/>[https://www.ncbi.nlm.nih.gov/pubmed/27627798]
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[https://www.ncbi.nlm.nih.gov/pubmed/28121234]
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<references/>[https://www.ncbi.nlm.nih.gov/pubmed/28121234]
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[https://www.ncbi.nlm.nih.gov/pubmed/?term=27373337]
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<references/>[https://www.ncbi.nlm.nih.gov/pubmed/?term=27373337]
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<references/>
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Revision as of 16:16, 23 December 2018

This Sandbox is Reserved from 06/12/2018, through 30/06/2019 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1480 through Sandbox Reserved 1543.
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  • Click the 3D button (when editing, above the wikitext box) to insert Jmol.
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Crystal structure of the catalytic domains of Mettl3/Mettl14 complex

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The complex METTL3/METTL14 is a heterodimer enzymatic complex involved into RNA post-transcription modifications. This complex is abble to add a methyl group on adenosin of the RNA, by catalyzing a m6(A) modification.The N(6)-methyladenosine (m(6)A) is a quite common, reversible chemical modification of functional RNAs which plays a key role in several biological fonctions.

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References

<Structural basis of N(6)-adenosine methylation by the METTL3-METTL14 complex./>[1]

  1. ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. ↑ Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
[2]

[3] [4] [5]


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