Literature DB >> 15452431

Mars -- robust automatic backbone assignment of proteins.

Young-Sang Jung1, Markus Zweckstetter.   

Abstract

MARS a program for robust automatic backbone assignment of (13)C/(15)N labeled proteins is presented. MARS does not require tight thresholds for establishing sequential connectivity or detailed adjustment of these thresholds and it can work with a wide variety of NMR experiments. Using only (13)C(alpha)/(13)C(beta) connectivity information, MARS allows automatic, error-free assignment of 96% of the 370-residue maltose-binding protein. MARS can successfully be used when data are missing for a substantial portion of residues or for proteins with very high chemical shift degeneracy such as partially or fully unfolded proteins. Other sources of information, such as residue specific information or known assignments from a homologues protein, can be included into the assignment process. MARS exports its result in SPARKY format. This allows visual validation and integration of automated and manual assignment.

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Year:  2004        PMID: 15452431     DOI: 10.1023/B:JNMR.0000042954.99056.ad

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  38 in total

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Journal:  J Biomol NMR       Date:  1994-01       Impact factor: 2.835

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Journal:  J Biomol NMR       Date:  1995-07       Impact factor: 2.835

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Journal:  J Biomol NMR       Date:  1995-11       Impact factor: 2.835

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Authors:  A Liu; R Riek; G Wider; C von Schroetter; R Zahn; K Wüthrich
Journal:  J Biomol NMR       Date:  2000-02       Impact factor: 2.835

9.  Automated backbone assignment of labeled proteins using the threshold accepting algorithm.

Authors:  M Leutner; R M Gschwind; J Liermann; C Schwarz; G Gemmecker; H Kessler
Journal:  J Biomol NMR       Date:  1998-01       Impact factor: 2.835

10.  1H-15N heteronuclear NMR studies of Escherichia coli thioredoxin in samples isotopically labeled by residue type.

Authors:  D M LeMaster; F M Richards
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  121 in total

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7.  Backbone resonance assignment of the homodimeric, 35 kDa chaperone CesT from enteropathogenic Escherichia coli.

Authors:  Sigrun Rumpel; Hai-Young Kim; Vinesh Vijayan; Stefan Becker; Markus Zweckstetter
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Authors:  Jianyong Wang; Tianzhi Wang; Erik R P Zuiderweg; Gordon M Crippen
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9.  Chemical shift assignments of a reduced N-terminal truncation mutant of the disulfide bond isomerase TrbB from plasmid F, TrbBΔ29.

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