FANTEN: a new web-based interface for the analysis of magnetic anisotropy-induced NMR data
- PMID: 25416616
- DOI: 10.1007/s10858-014-9877-4
FANTEN: a new web-based interface for the analysis of magnetic anisotropy-induced NMR data
Abstract
Pseudocontact shifts (PCSs) and residual dipolar couplings (RDCs) arising from the presence of paramagnetic metal ions in proteins as well as RDCs due to partial orientation induced by external orienting media are nowadays routinely measured as a part of the NMR characterization of biologically relevant systems. PCSs and RDCs are becoming more and more popular as restraints (1) to determine and/or refine protein structures in solution, (2) to monitor the extent of conformational heterogeneity in systems composed of rigid domains which can reorient with respect to one another, and (3) to obtain structural information in protein-protein complexes. The use of both PCSs and RDCs proceeds through the determination of the anisotropy tensors which are at the origin of these NMR observables. A new user-friendly web tool, called FANTEN (Finding ANisotropy TENsors), has been developed for the determination of the anisotropy tensors related to PCSs and RDCs and has been made freely available through the WeNMR ( http://fanten-enmr.cerm.unifi.it:8080 ) gateway. The program has many new features not available in other existing programs, among which the possibility of a joint analysis of several sets of PCS and RDC data and the possibility to perform rigid body minimizations.
Similar articles
-
MaxOcc: a web portal for maximum occurrence analysis.J Biomol NMR. 2012 Aug;53(4):271-80. doi: 10.1007/s10858-012-9638-1. Epub 2012 May 26. J Biomol NMR. 2012. PMID: 22639196
-
Paramagpy: software for fitting magnetic susceptibility tensors using paramagnetic effects measured in NMR spectra.Magn Reson (Gott). 2020 Feb 14;1(1):1-12. doi: 10.5194/mr-1-1-2020. eCollection 2020. Magn Reson (Gott). 2020. PMID: 37904891 Free PMC article.
-
15N-1H Residual dipolar coupling analysis of native and alkaline-K79A Saccharomyces cerevisiae cytochrome c.Biophys J. 2003 Jun;84(6):3917-23. doi: 10.1016/S0006-3495(03)75119-4. Biophys J. 2003. PMID: 12770897 Free PMC article.
-
Structure determination of protein-protein complexes with long-range anisotropic paramagnetic NMR restraints.Curr Opin Struct Biol. 2014 Feb;24:45-53. doi: 10.1016/j.sbi.2013.11.010. Epub 2013 Dec 21. Curr Opin Struct Biol. 2014. PMID: 24721452 Review.
-
The use of residual dipolar coupling in studying proteins by NMR.Top Curr Chem. 2012;326:47-67. doi: 10.1007/128_2011_215. Top Curr Chem. 2012. PMID: 21952837 Free PMC article. Review.
Cited by
-
Joint X-ray/NMR structure refinement of multidomain/multisubunit systems.J Biomol NMR. 2019 Jul;73(6-7):265-278. doi: 10.1007/s10858-018-0212-3. Epub 2018 Oct 11. J Biomol NMR. 2019. PMID: 30311122 Free PMC article.
-
A protocol for the refinement of NMR structures using simultaneously pseudocontact shift restraints from multiple lanthanide ions.J Biomol NMR. 2016 Nov;66(3):175-185. doi: 10.1007/s10858-016-0065-6. Epub 2016 Oct 22. J Biomol NMR. 2016. PMID: 27771862
-
Real-Time Insights into Biological Events: In-Cell Processes and Protein-Ligand Interactions.Biophys J. 2019 Jan 22;116(2):239-247. doi: 10.1016/j.bpj.2018.11.3132. Epub 2018 Dec 6. Biophys J. 2019. PMID: 30580921 Free PMC article.
-
Assessing Structural Preferences of Unstructured Protein Regions by NMR.Biophys J. 2019 Nov 19;117(10):1948-1953. doi: 10.1016/j.bpj.2019.10.008. Epub 2019 Oct 14. Biophys J. 2019. PMID: 31676138 Free PMC article.
-
Long-range paramagnetic NMR data can provide a closer look on metal coordination in metalloproteins.J Biol Inorg Chem. 2018 Jan;23(1):71-80. doi: 10.1007/s00775-017-1511-y. Epub 2017 Dec 7. J Biol Inorg Chem. 2018. PMID: 29218635
References
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources