A comparison of genotype-phenotype maps for RNA and proteins.
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[1] C. Sander,et al. Database of homology‐derived protein structures and the structural meaning of sequence alignment , 1991, Proteins.
[2] Paul Schimmel,et al. Incorporation of nonnatural amino acids into proteins. , 2004, Annual review of biochemistry.
[3] E. Bornberg-Bauer,et al. How are model protein structures distributed in sequence space? , 1997, Biophysical journal.
[4] Devarajan Thirumalai,et al. Kinetics of Folding of Proteins and RNA , 1996 .
[5] E. Gumbel,et al. Statistics of extremes , 1960 .
[6] P. Stadler,et al. Conserved RNA secondary structures in Flaviviridae genomes. , 2004, The Journal of general virology.
[7] D. Baker,et al. Functional rapidly folding proteins from simplified amino acid sequences , 1997, Nature Structural Biology.
[8] P. Schuster,et al. Analysis of RNA sequence structure maps by exhaustive enumeration II. Structures of neutral networks and shape space covering , 1996 .
[9] Udayan Mohanty,et al. Compact and ordered collapse of randomly generated RNA sequences , 2005, Nature Structural &Molecular Biology.
[10] L. Chew,et al. Unit‐vector RMS (URMS) as a tool to analyze molecular dynamics trajectories , 1999, Proteins.
[11] Marc A. Martí-Renom,et al. Quantifying the relationship between sequence and three-dimensional structure conservation in RNA , 2009, BMC Bioinformatics.
[12] W. Fontana. Modelling 'evo-devo' with RNA. , 2002, BioEssays : news and reviews in molecular, cellular and developmental biology.
[13] A. Wagner. Robustness and evolvability: a paradox resolved , 2008, Proceedings of the Royal Society B: Biological Sciences.
[14] A. Lesk,et al. The relation between the divergence of sequence and structure in proteins. , 1986, The EMBO journal.
[15] Marc A. Martí-Renom,et al. RNA structure alignment by a unit-vector approach , 2008, ECCB.
[16] Walter Fontana,et al. Fast folding and comparison of RNA secondary structures , 1994 .
[17] D. Yee,et al. Principles of protein folding — A perspective from simple exact models , 1995, Protein science : a publication of the Protein Society.
[18] P. Schuster,et al. Analysis of RNA sequence structure maps by exhaustive enumeration I. Neutral networks , 1995 .
[19] Erich Bornberg-Bauer,et al. Perspectives on protein evolution from simple exact models. , 2002, Applied bioinformatics.
[20] K. Dill,et al. A lattice statistical mechanics model of the conformational and sequence spaces of proteins , 1989 .
[21] Andreas Wagner,et al. The Origins of Evolutionary Innovations: A Theory of Transformative Change in Living Systems , 2011 .
[22] P. Schuster,et al. From sequences to shapes and back: a case study in RNA secondary structures , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[23] N. Cuceanu,et al. Evolutionarily conserved RNA secondary structures in coding and non-coding sequences at the 3' end of the hepatitis G virus/GB-virus C genome. , 2001, The Journal of general virology.
[24] John Maynard Smith,et al. Natural Selection and the Concept of a Protein Space , 1970, Nature.
[25] P. Schuster,et al. Discrete Models of Biopolymers , 2007 .
[26] Carl Troein,et al. Enumerating Designing Sequences in the HP Model , 2002, Journal of biological physics.
[27] P. Schuster,et al. IR-98-039 / April Continuity in Evolution : On the Nature of Transitions , 1998 .
[28] Harjinder Singh,et al. Base pairing in RNA structures: A computational analysis of structural aspects and interaction energies , 2007 .
[29] Nicolas E. Buchler,et al. Effect of alphabet size and foldability requirements on protein structure designability , 1999, Proteins.
[30] R. Sauer,et al. Folded proteins occur frequently in libraries of random amino acid sequences. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[31] R. Levy,et al. Simplified amino acid alphabets for protein fold recognition and implications for folding. , 2000, Protein engineering.
[32] T. Yomo,et al. Solubility of artificial proteins with random sequences , 1996, FEBS letters.
[33] A. G. Brevern,et al. A reduced amino acid alphabet for understanding and designing protein adaptation to mutation , 2007, European Biophysics Journal.
[34] G. F. Joyce,et al. A ribozyme composed of only two different nucleotides , 2002, Nature.
[35] Robert T. Sauer,et al. Cooperatively folded proteins in random sequence libraries , 1995, Nature Structural Biology.
[36] Gerald F. Joyce,et al. A ribozyme that lacks cytidine , 1999, Nature.
[37] Andreas Wagner,et al. New structural variation in evolutionary searches of RNA neutral networks , 2006, Biosyst..
[38] J Abelson,et al. Evolution of a transfer RNA gene through a point mutation in the anticodon. , 1998, Science.
[39] Yingfu Li,et al. DNAzyme-mediated catalysis with only guanosine and cytidine nucleotides , 2008, Nucleic acids research.
[40] L. H. Bradley,et al. De novo proteins from designed combinatorial libraries , 2004, Protein science : a publication of the Protein Society.
[41] J. Szostak,et al. In vitro selection of functional nucleic acids. , 1999, Annual review of biochemistry.
[42] A. Wagner,et al. Evolutionary Innovations and the Organization of Protein Functions in Genotype Space , 2010, PloS one.
[43] M. Distefano,et al. Generation of New Enzymes via Covalent Modification of Existing Proteins , 2001 .
[44] D. Lipman,et al. Modelling neutral and selective evolution of protein folding , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[45] D. Thirumalai,et al. RNA and protein folding: common themes and variations. , 2005, Biochemistry.
[46] E. Bornberg-Bauer,et al. Modeling evolutionary landscapes: mutational stability, topology, and superfunnels in sequence space. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[47] W. Kauzmann. Some factors in the interpretation of protein denaturation. , 1959, Advances in protein chemistry.
[48] P. Schuster,et al. Statistics of RNA secondary structures , 1993, Biopolymers.
[49] Thirumalai,et al. Minimum energy compact structures of random sequences of heteropolymers. , 1993, Physical review letters.
[50] N. Wingreen,et al. Emergence of Preferred Structures in a Simple Model of Protein Folding , 1996, Science.
[51] W. Hendrickson,et al. Quantification of tertiary structural conservation despite primary sequence drift in the globin fold , 1994, Protein science : a publication of the Protein Society.
[52] M. Huynen. Exploring phenotype space through neutral evolution , 1996, Journal of Molecular Evolution.
[53] R. Hardison,et al. A brief history of hemoglobins: plant, animal, protist, and bacteria. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[54] Osvaldo Olmea,et al. MAMMOTH (Matching molecular models obtained from theory): An automated method for model comparison , 2002, Protein science : a publication of the Protein Society.
[55] P. Stadler,et al. Neutral networks in protein space: a computational study based on knowledge-based potentials of mean force. , 1997, Folding & design.
[56] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..