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Abstract: Large macromolecular complexes such as the 16S ribosomal RNA (16S rRNA) frustrate traditional experimental methods of structure determination that succeed with smaller molecules. These large complexes often contain both protein and nucleic acid components composed of thousands of atoms, making them intractable to X-ray crystallographic techniques. Extensive biochemical studies of these macromolecules, however, often yield useful, though sparse, structural information by revealing particular... (Update)
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...to combat low quality locally optimal solutions which may be encountered by analytical procedures such as the current algorithm. See [7] for details of the problem and its computation. The decomposition of the 30S ribosome problem is indicated in Figure 4. The execution...
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BibTeX entry: (Update)
Chen, R., D. Fink, R. B. Altman, "Computing the Structure of Large Complexes: Applying Constraint Satisfaction Techniques to Modeling the 16S Ribosomal RNA", Biomolecular NMR Spectroscopy (Markley, J. L. and S. J. Opella, eds.), pp.279--299, Oxford University Press, 1995. http://citeseer.ist.psu.edu/chen95computing.html More
@misc{ chen95computing,
author = "R. Chen and D. Fink and R. Altman",
title = "Computing the Structure of Large Complexes: Applying Constraint Satisfaction
Techniques to Modeling the 16S Ribosomal RNA",
text = "Chen, R., D. Fink, R. B. Altman, Computing the Structure of Large Complexes:
Applying Constraint Satisfaction Techniques to Modeling the 16S Ribosomal
RNA, Biomolecular NMR Spectroscopy (Markley, J. L. and S. J. Opella, eds.),
pp.279--299, Oxford University Press, 1995.",
year = "1995",
url = "citeseer.ist.psu.edu/chen95computing.html" }
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