3f2e

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Current revision (06:37, 3 April 2024) (edit) (undo)
 
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== Function ==
== Function ==
[https://www.uniprot.org/uniprot/D0VX05_9VIRU D0VX05_9VIRU]
[https://www.uniprot.org/uniprot/D0VX05_9VIRU D0VX05_9VIRU]
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== Publication Abstract from PubMed ==
 
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NMR spectroscopy and X-ray crystallography are currently the two most widely applied methods for the determination of macromolecular structures at high resolution. More recently, significant advances have been made in algorithms for the de novo prediction of protein structure, and, in favorable cases, the predicted models agree extremely well with experimentally determined structures. Here, we demonstrate a synergistic combination of NMR spectroscopy, de novo structure prediction, and X-ray crystallography in an effective overall strategy for rapidly determining the structure of the coat protein C-terminal domain from the Sulfolobus islandicus rod-shaped virus (SIRV). This approach takes advantage of the most accessible aspects of each structural technique and may be widely applicable for structure determination.
 
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Synergy of NMR, computation, and X-ray crystallography for structural biology.,Szymczyna BR, Taurog RE, Young MJ, Snyder JC, Johnson JE, Williamson JR Structure. 2009 Apr 15;17(4):499-507. PMID:19368883<ref>PMID:19368883</ref>
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==See Also==
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*[[Virus coat proteins 3D structures|Virus coat proteins 3D structures]]
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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<div class="pdbe-citations 3f2e" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
</StructureSection>

Current revision

Crystal structure of Yellowstone SIRV coat protein C-terminus

PDB ID 3f2e

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