Literature DB >> 15318004

NOE assignment with ARIA 2.0: the nuts and bolts.

Michael Habeck1, Wolfgang Rieping, Jens P Linge, Michael Nilges.   

Abstract

The assignment of nuclear Overhauser effect (NOE) resonances is the crucial step in determining the three-dimensional structure of biomolecules from nuclear magnetic resonance (NMR) data. Our program, Ambiguous Restraints for Iterative Assignment (ARIA), treats Noe assignment as an integral part of the structure determination process. This chapter briefly outlines the method and discusses how to carry out a complete structure determination project with the new version 2.0 of ARIA. Two new features greatly streamline the procedure: a new graphical user interface (GUI) and the incorporation of the data model of the Collaborative Computing Project for the NMR community (CCPN). The GUI supports the user in setting up and managing a project. The CCPN data model facilitates data exchange with a great variety of other programs. We give practical guidelines for how to use ARIA and how to analyze results.

Mesh:

Substances:

Year:  2004        PMID: 15318004     DOI: 10.1385/1-59259-809-9:379

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  24 in total

1.  Structural studies of E73 from a hyperthermophilic archaeal virus identify the "RH3" domain, an elaborated ribbon-helix-helix motif involved in DNA recognition.

Authors:  Casey Schlenker; Anupam Goel; Brian P Tripet; Smita Menon; Taylor Willi; Mensur Dlakić; Mark J Young; C Martin Lawrence; Valérie Copié
Journal:  Biochemistry       Date:  2012-03-22       Impact factor: 3.162

2.  Solution structure of a late embryogenesis abundant protein (LEA14) from Arabidopsis thaliana, a cellular stress-related protein.

Authors:  Shanteri Singh; Claudia C Cornilescu; Robert C Tyler; Gabriel Cornilescu; Marco Tonelli; Min S Lee; John L Markley
Journal:  Protein Sci       Date:  2005-09-09       Impact factor: 6.725

3.  NMR solution structure and backbone dynamics of domain III of the E protein of tick-borne Langat flavivirus suggests a potential site for molecular recognition.

Authors:  Munia Mukherjee; Kaushik Dutta; Mark A White; David Cowburn; Robert O Fox
Journal:  Protein Sci       Date:  2006-06       Impact factor: 6.725

4.  Solution conformation of the His-47 to Ala-47 mutant of Pseudomonas stutzeri ZoBell ferrocytochrome c-551.

Authors:  Qiaoli Liang; Gregory T Miller; Chanda A Beeghley; Coyner B Graf; Russell Timkovich
Journal:  Biophys J       Date:  2007-05-11       Impact factor: 4.033

5.  Solution structure of Ca2+-free rat alpha-parvalbumin.

Authors:  Michael T Henzl; John J Tanner
Journal:  Protein Sci       Date:  2008-01-24       Impact factor: 6.725

Review 6.  Automated structure determination from NMR spectra.

Authors:  Peter Güntert
Journal:  Eur Biophys J       Date:  2008-09-20       Impact factor: 1.733

7.  Analysis of the performance of the CHESHIRE and YAPP methods at CASD-NMR round 3.

Authors:  Andrea Cavalli; Michele Vendruscolo
Journal:  J Biomol NMR       Date:  2015-05-20       Impact factor: 2.835

8.  A unified NMR strategy for high-throughput determination of backbone fold of small proteins.

Authors:  Dinesh Kumar; Anmol Gautam; Ramakrishna V Hosur
Journal:  J Struct Funct Genomics       Date:  2012-09-28

9.  Solution structure of Ca2+-free rat beta-parvalbumin (oncomodulin).

Authors:  Michael T Henzl; John J Tanner
Journal:  Protein Sci       Date:  2007-09       Impact factor: 6.725

10.  Structure of the C-Terminal Helical Repeat Domain of Eukaryotic Elongation Factor 2 Kinase.

Authors:  Nathan Will; Andrea Piserchio; Isaac Snyder; Scarlet B Ferguson; David H Giles; Kevin N Dalby; Ranajeet Ghose
Journal:  Biochemistry       Date:  2016-09-14       Impact factor: 3.162

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