Molecular mechanics calculations on deaminooxytocin and on deamino-arginine-vasopressin and its analogues
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[1] P. Flory,et al. Structural Geometry and Torsional Potentials in p-Phenylene Polyamides and Polyesters , 1980 .
[2] T. Schaefer,et al. A proton magnetic resonance determination of the barrier to internal rotation in benzenethiol in solution , 1977 .
[3] T. Blundell,et al. Crystal structure analysis of deamino-oxytocin: conformational flexibility and receptor binding. , 1988, Science.
[4] J. B. Willis,et al. 295. The infra-red spectra and chemical structure of some aromatic disulphides, disulphones, and thiolsulphonates , 1951 .
[5] E. M. Popov. Quantitative approach to conformations of proteins , 1979 .
[6] R. Kniseley,et al. Infrared spectra of nitrogen containing compounds—I: Benzamide , 1962 .
[7] R. Hughes,et al. Structure of pressinoic acid: the cyclic moiety of vasopressin. , 1986, Science.
[8] P. Birner,et al. Success of the NDDO method to predict conformations in conjugated systems , 1976 .
[9] M. Flett. Intensities of some group characteristic infra-red bands , 1962 .
[10] G. Chipens,et al. Theoretical conformational analysis of oxytocin molecule. , 2009, International journal of peptide and protein research.
[11] D. J. Harrison,et al. Vibrational spectra of benzene derivatives—XXI. Benzoyl fluoride, acetophenone, methyl benzoate and related compounds , 1977 .
[12] M. Manning,et al. Synthesis and some pharmacological properties of deamino(4-threonine,8-D-arginine)vasopressin and deamino(8-D-arginine)vasopressin, highly potent and specific antidiuretic peptides, and (8-D-arginine)vasopressin and deamino-arginine-vasopressin. , 1976, Journal of medicinal chemistry.
[13] M. Manning,et al. [1-beta-Mercapto-beta,beta-cyclopentamethylenepropionic acid),2-(O-methyl)tyrosine ]argine-vasopressin and [1-beta-mercapto-beta,beta-cyclopentamethylenepropionic acid)]argine-vasopressine, two highly potent antagonists of the vasopressor response to arginine-vasopressin. , 1980, Journal of medicinal chemistry.
[14] S. Rackovsky,et al. Differential Geometry and Polymer Conformation. 1. Comparison of Protein Conformations1a,b , 1978 .
[15] H. Scheraga,et al. Raman spectra of cystine-related disulfides. Effect of rotational isomerism about carbon-sulfur bonds on sulfur-sulfur stretching frequencies , 1976 .
[16] C. Blake,et al. The crystal structure of benzamide , 1972 .
[17] H. Scheraga,et al. Energy parameters in polypeptides. VII. Geometric parameters, partial atomic charges, nonbonded interactions, hydrogen bond interactions, and intrinsic torsional potentials for the naturally occurring amino acids , 1975 .
[18] D. Urry,et al. Proposed conformation of oxytocin in solution. , 1971, Proceedings of the National Academy of Sciences of the United States of America.
[19] M. Manning,et al. Solid-phase synthesis and some pharmacological properties of 4-threonine analogs of vasopressins and vasotocin and of arginine-vasopressin and arginine-vasotocin. , 1973, Journal of medicinal chemistry.
[20] S. Rackovsky,et al. Differential Geometry and Polymer Conformation. 2. Development of a Conformational Distance Function , 1980 .
[21] R. Deslauriers,et al. A carbon-13 nuclear magnetic resonance study of oxytocin and its oligopeptides. , 1972, Biochemical and biophysical research communications.
[22] M. Sacerdoti,et al. Comparison of two independent structure determinations of diphenyl disulphide , 1975 .
[23] T. Blundell,et al. The conformation, flexibility, and dynamics of polypeptide hormones. , 1982, Annual review of biochemistry.
[24] U. Singh,et al. A NEW FORCE FIELD FOR MOLECULAR MECHANICAL SIMULATION OF NUCLEIC ACIDS AND PROTEINS , 1984 .