MOTIVATION: Nuclear magnetic resonance (NMR) spectroscopy is widely used to determine and analyze protein structures. An essential step in NMR studies is determining the backbone resonance assignment, which maps individual atoms to experimentally measured resonance frequencies. Performing assignment is challenging owing to the noise and ambiguity in NMR spectra. Although automated procedures have been investigated, by-and-large they are still struggling to gain acceptance because of inherent limits in scalability and/or unacceptable levels of assignment error. To have confidence in the results, an algorithm should be complete, i.e. able to identify all solutions consistent with the data, including all arbitrary configurations of extra and missing peaks. The ensuing combinatorial explosion in the space of possible assignments has led to the perception that complete search is hopelessly inefficient and cannot scale to realistic datasets. RESULTS: This paper presents a complete branch-contract-and-bound search algorithm for backbone resonance assignment. The algorithm controls the search space by hierarchically agglomerating partial assignments and employing statistically sound pruning criteria. It considers all solutions consistent with the data, and uniformly treats all combinations of extra and missing data. We demonstrate our approach on experimental data from five proteins ranging in size from 70 to 154 residues. The algorithm assigns >95% of the positions with >98% accuracy. We also present results on simulated data from 259 proteins from the RefDB database, ranging in size from 25 to 257 residues. The median computation time for these cases is 1 min, and the assignment accuracy is >99%. These results demonstrate that complete search not only has the advantage of guaranteeing fair treatment of all feasible solutions, but is efficient enough to be employed effectively inpractice. AVAILABILITY: The MBA(2) software package is made available under an open-source software license. The datasets featured in the Results section can also be obtained from the contact author.
[NMR paper] NMR backbone assignment of the mitogen-activated protein (MAP) kinase p38.
NMR backbone assignment of the mitogen-activated protein (MAP) kinase p38.
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J Biomol NMR. 2005 Jun;32(2):175
Authors: Vogtherr M, Saxena K, Grimme S, Betz M, Schieborr U, Pescatore B, Langer T, Schwalbe H
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[NMR paper] Complete assignment of heteronuclear protein resonances by protonless NMR spectroscop
Complete assignment of heteronuclear protein resonances by protonless NMR spectroscopy.
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Angew Chem Int Ed Engl. 2005 May 13;44(20):3089-92
Authors: Bermel W, Bertini I, Duma L, Felli IC, Emsley L, Pierattelli R, Vasos PR
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[NMR paper] G-matrix Fourier transform NMR spectroscopy for complete protein resonance assignment
G-matrix Fourier transform NMR spectroscopy for complete protein resonance assignment.
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Proc Natl Acad Sci U S A. 2004 Jun 29;101(26):9642-7
Authors: Atreya HS, Szyperski T
A G-matrix Fourier transform (GFT) NMR spectroscopy-based strategy for resonance assignment of proteins is described. Each of the GFT NMR experiments presented here rapidly affords four-, five-, or six-dimensional spectral information in combination with precise...
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[NMR paper] An efficient branch-and-bound algorithm for the assignment of protein backbone NMR pe
An efficient branch-and-bound algorithm for the assignment of protein backbone NMR peaks.
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Proc IEEE Comput Soc Bioinform Conf. 2002;1:165-74
Authors: Lin G, Xu D, Chen ZZ, Jiang T, Wen J, Xu Y
NMR resonance assignment is one of the key steps in solving an NMR protein structure. The assignment process links resonance peaks to individual residues of the target protein sequence, providing the prerequisite for establishing intra- and...
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[NMR paper] Toward solving the folding pathway of barnase: the complete backbone 13C, 15N, and 1H
Toward solving the folding pathway of barnase: the complete backbone 13C, 15N, and 1H NMR assignments of its pH-denatured state.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www.pubmedcentral.nih.gov-corehtml-pmc-pmcgifs-pubmed-pmc.gif Related Articles Toward solving the folding pathway of barnase: the complete backbone 13C, 15N, and 1H NMR assignments of its pH-denatured state.
Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9412-6
Authors: Arcus VL, Vuilleumier S, Freund SM, Bycroft M, Fersht AR
The structures of the major folding...
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[NMR paper] Sequential assignment of 2D-NMR spectra of proteins using genetic algorithms.
Sequential assignment of 2D-NMR spectra of proteins using genetic algorithms.
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J Chem Inf Comput Sci. 1993 Mar-Apr;33(2):245-51
Authors: Wehrens R, Lucasius C, Buydens L, Kateman G
The application of genetic algorithms to the problem of the sequential assignment of two-dimensional protein NMR spectra is discussed. The problem is heavily underconstrained since in most cases more patterns are available than amino acid positions, and uncertainties may...
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[NMR paper] Computer-assisted assignment of 2D 1H NMR spectra of proteins: basic algorithms and a
Computer-assisted assignment of 2D 1H NMR spectra of proteins: basic algorithms and application to phoratoxin B.
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J Biomol NMR. 1991 May;1(1):23-47
Authors: Kleywegt GJ, Boelens R, Cox M, Llinás M, Kaptein R
A suite of computer programs (CLAIRE) is described which can be of assistance in the process of assigning 2D 1H NMR spectra of proteins. The programs embody a software implementation of the sequential assignment...
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[NMR paper] Complete resonance assignment for the polypeptide backbone of interleukin 1 beta usin
Complete resonance assignment for the polypeptide backbone of interleukin 1 beta using three-dimensional heteronuclear NMR spectroscopy.
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Biochemistry. 1990 Apr 10;29(14):3542-56
Authors: Driscoll PC, Clore GM, Marion D, Wingfield PT, Gronenborn AM
The complete sequence-specific assignment of the 15N and 1H backbone resonances of the NMR spectrum of recombinant human interleukin 1 beta (153...