Studies on the specificity of HIV protease: An application of Markov chain theory
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[1] J Sninsky,et al. HIV-1 isolates are rapidly evolving quasispecies: evidence for viral mixtures and preferred nucleotide substitutions. , 1989, Journal of acquired immune deficiency syndromes.
[2] A Wlodawer,et al. Structure of complex of synthetic HIV-1 protease with a substrate-based inhibitor at 2.3 A resolution. , 1989, Science.
[3] P Martel,et al. Biophysical aspects of neutron scattering from vibrational modes of proteins. , 1992, Progress in biophysics and molecular biology.
[4] T. Copeland,et al. Molecular characterization of gag proteins from simian immunodeficiency virus (SIVMne) , 1988, Journal of virology.
[5] A. Meyerhans,et al. Selection, recombination, and G----A hypermutation of human immunodeficiency virus type 1 genomes , 1991, Journal of virology.
[6] J. Louis,et al. Kinetic and modeling studies of S3-S3' subsites of HIV proteinases. , 1992, Biochemistry.
[7] K. Chou,et al. A vectorized sequence-coupling model for predicting HIV protease cleavage sites in proteins. , 1993, The Journal of biological chemistry.
[8] John P. Overington,et al. X-ray analysis of HIV-1 proteinase at 2.7 Å resolution confirms structural homology among retroviral enzymes , 1989, Nature.
[9] M. Jaskólski,et al. Conserved folding in retroviral proteases: crystal structure of a synthetic HIV-1 protease. , 1989, Science.
[10] J. Chermann,et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). , 1983, Science.
[11] Gregory K. Miller,et al. Elements of Applied Stochastic Processes , 1972 .
[12] S. Wain-Hobson. HIV genome variability in vivo , 1989, AIDS.
[13] T. Miyata,et al. Retroviral protease-like sequence in the yeast transposon Ty 1 , 1985, Nature.
[14] B. Haynes,et al. Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS. , 1984, Science.
[15] B. Efron. The jackknife, the bootstrap, and other resampling plans , 1987 .
[16] E. Wimmer,et al. Proteolytic processing of polyproteins in the replication of RNA viruses. , 1989, Biochemistry.
[17] A. Wlodawer,et al. Different requirements for productive interaction between the active site of HIV-1 proteinase and substrates containing -hydrophobic*hydrophobic- or -aromatic*pro- cleavage sites. , 1992, Biochemistry.
[18] L J Davis,et al. Active human immunodeficiency virus protease is required for viral infectivity. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[19] A. Berger,et al. On the size of the active site in proteases. I. Papain. , 1967, Biochemical and biophysical research communications.
[20] E. Wimmer,et al. Mutational analysis of a native substrate of the human immunodeficiency virus type 1 proteinase , 1990, Journal of virology.
[21] M. Navia,et al. Three-dimensional structure of aspartyl protease from human immunodeficiency virus HIV-1 , 1989, Nature.
[22] K. Chou,et al. A correlation-coefficient method to predicting protein-structural classes from amino acid compositions. , 1992, European journal of biochemistry.
[23] K. Chou,et al. Monte Carlo simulation studies on the prediction of protein folding types from amino acid composition. , 1992, Biophysical journal.
[24] C. Zhang,et al. Diagrammatization of codon usage in 339 human immunodeficiency virus proteins and its biological implication. , 1992, AIDS research and human retroviruses.
[25] S. Swaminathan,et al. Molecular dynamics of HIV‐1 protease , 1992, Proteins.
[26] J. Mrázek,et al. Unusual codon usage of HIV , 1987, Nature.
[27] William R. Taylor,et al. A structural model for the retroviral proteases , 1987, Nature.
[28] What can AIDS virus codon usage tell us? , 1986, Nature.
[29] W. Kabsch,et al. How good are predictions of protein secondary structure? , 1983, FEBS letters.