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Pure Appl. Chem., 1974, Vol. 40, No. 3, pp. 291-308

http://dx.doi.org/10.1351/pac197440030291

IUPAC-IUB COMMISSION ON BIOCHEMICAL NOMENCLATURE

Abbreviations and symbols for description of conformation of polypeptide chains (Rules approved 1974)

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  • Gordon Mark S., Fedorov Dmitri G., Pruitt Spencer R., Slipchenko Lyudmila V.: Fragmentation Methods: A Route to Accurate Calculations on Large Systems. Chemistry Review 2012, 112, 632. <http://dx.doi.org/10.1021/cr200093j>
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  • Brut Marie, Estève Alain, Landa Georges, Dkhissi Ahmed, Renvez Guillaume, Rouhani Mehdi Djafari, Gauchard David: Atomic-scale determination of DNA conformational response to strained furanose: a static mode approach. Tetrahedron 2010, 66, 9123. <http://dx.doi.org/10.1016/j.tet.2010.09.083>
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  • Wang Wei, Cai Minying, Xiong Chiyi, Zhang Junyi, Trivedi Dev, Hruby Victor J: Design and synthesis of novel χ2-constrained phenylalanine, naphthylalanine, and tryptophan analogues and their use in biologically active melanotropin peptides. Tetrahedron 2002, 58, 7365. <http://dx.doi.org/10.1016/S0040-4020(02)00588-4>
  • Hruby Victor J., Li Guigen, Haskell-Luevano Carrie, Shenderovich Mark: Design of peptides, proteins, and peptidomimetics in chi space. Biopolymers (Biospectroscopy) 1997, 43, 219. <http://dx.doi.org/10.1002/(SICI)1097-0282(1997)43:3<219::AID-BIP3>3.0.CO;2-Y>
  • Liao Subo, Shenderovich Mark D., Lin Jun, Hruby Victor J.: Synthesis and conformational features of topographically constrained designer chimeric amino acids: The β-isopropyl phenylalanines. Tetrahedron 1997, 53, 16645. <http://dx.doi.org/10.1016/S0040-4020(97)10127-2>
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  • Nikiforovich G.V., Rozenblit S.A., Shenderovich M.D., Chipens G.I.: Possible bioactive conformations of α-melanotropin. FEBS Letters 1984, 170, 315. <http://dx.doi.org/10.1016/0014-5793(84)81335-6>
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  • Stensland Birgitta, Castensson Staffan: X-ray conformational analysis of the potent thyroliberin analogue l-pyroglutamyl-β-(2-thienyl)-l-alanyl-l-prolinamide. Journal of Molecular Biology 1982, 161, 257. <http://dx.doi.org/10.1016/0022-2836(82)90152-8>