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Title: Structure calculation, refinement and validation using CcpNmr Analysis
Authors: Skinner, Simon P.
Goult, Benjamin T.
Fogh, Rasmus H.
Boucher, W.
Stevens, T. J.
Laue, E. D.
Vuister, Geerten W.
First Published: Jan-2015
Publisher: International Union of Crystallography, Wiley
Citation: Acta Crystallographica Section D: Biological Crystallography, D71, pp. 154-161
Abstract: CcpNmr Analysis provides a streamlined pipeline for both NMR chemical shift assignment and structure determination of biological macromolecules. In addition, it encompasses tools to analyse the many additional experiments that make NMR such a pivotal technique for research into complex biological questions. This report describes how CcpNmr Analysis can seamlessly link together all of the tasks in the NMR structure-determination process. It details each of the stages from generating NMR restraints [distance, dihedral, hydrogen bonds and residual dipolar couplings (RDCs)], exporting these to and subsequently re-importing them from structure-calculation software (such as the programs CYANA or ARIA) and analysing and validating the results obtained from the structure calculation to, ultimately, the streamlined deposition of the completed assignments and the refined ensemble of structures into the PDBe repository. Until recently, such solution-structure determination by NMR has been quite a laborious task, requiring multiple stages and programs. However, with the new enhancements to CcpNmr Analysis described here, this process is now much more intuitive and efficient and less error-prone.
DOI Link: 10.1107/S1399004714026662
ISSN: 0907-4449
eISSN: 1399-0047
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Archived with reference to SHERPA/RoMEO. Version of record:
Appears in Collections:Published Articles, Dept. of Biochemistry

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