Structural versatility of peptides from Cα,α-dialkylated glycines: a conformational energy calculation and X-ray diffraction study of homopeptides from 1-aminocyclopentane-1-carboxylic acid☆
暂无分享,去创建一个
Vincenzo Barone | Franca Fraternali | Claudio Toniolo | Antonello Santini | Francesco Lelj | Gian Maria Bonora | Vincenzo Pavone | Ettore Benedetti | V. Barone | C. Toniolo | M. Crisma | F. Fraternali | C. Pedone | E. Benedetti | A. Santini | A. Bavoso | B. D. Blasio | F. Lelj | V. Pavone | G. Bonora | Marco Crisma | B. Di Blasio | C. Pedone | Alfonso Bavoso | B. Blasio
[1] H. Scheraga,et al. Preferred conformation of the benzyloxycarbonyl-amino group in peptides. , 2009, International journal of peptide and protein research.
[2] V. Hruby,et al. Pharmacological, conformational and dynamic properties of cycloleucine-2 analogues of oxytocin and [1-penicillamine]oxytocin. , 2009, International journal of peptide and protein research.
[3] H. Scheraga,et al. Preferred conformation of the tert-butoxycarbonyl-amino group in peptides. , 2009, International journal of peptide and protein research.
[4] C. Toniolo,et al. Conformational analysis of N-(tert.-amyloxycarbony-L-proline in the solid state and in solution. , 2009, International journal of peptide and protein research.
[5] C. Ramakrishnan,et al. Analysis of O-H...O hydrogen bonds. , 2009, International journal of peptide and protein research.
[6] C. Ramakrishnan,et al. Study of hydrogen bonds in amino acids and peptides. , 2009, International journal of protein research.
[7] C. Toniolo,et al. Structural versatility of peptides from Cα,α-dialkylated glycines: an infrared absorption and 1H n.m.r. study of homopeptides from 1-aminocyclopentane-1-carboxylic acid , 1988 .
[8] C. Toniolo,et al. A novel peptide conformation: First unequivocal observation of the oxy‐analog of a β‐bend , 1986 .
[9] Claudio Toniolo,et al. Stereochemically constrained peptides. Theoretical and experimental studies on the conformations of peptides containing 1-aminocyclohexanecarboxylic acid , 1986 .
[10] C. Toniolo,et al. Stereochemistry of peptides containing 1‐aminocyclopentanecarboxylic acid (Acc5): Solution and solid‐state conformations of Boc‐Acc5‐Acc5‐NHMe , 1986 .
[11] C. Toniolo,et al. A long, regular polypeptide 310-helix , 1986 .
[12] J. Bland,et al. Peptide sweeteners. 8. Synthesis and structure-taste relationship studies of L-aspartyl-D-alanyl tripeptides. , 1985, Journal of medicinal chemistry.
[13] A. Essenburg,et al. Synthesis and biological activity of modified peptide inhibitors of angiotensin-converting enzyme. , 1985, Journal of medicinal chemistry.
[14] V. Barone,et al. FOLDED AND EXTENDED STRUCTURES OF HOMOOLIGOPEPTIDES FROM α,α‐DIALKYLATED GLYCINES. A CONFORMATIONAL ENERGY COMPUTATION AND X‐RAY DIFFRACTION STUDY , 1985 .
[15] P. Balaram,et al. A highly active chemotactic peptide analog incorporating the unusual residue 1-aminocyclohexanecarboxylic acid at position 2. , 1985, Biochemical and biophysical research communications.
[16] M. Goodman. Peptide homologs, isosteres, and isomers: A general approach to structure–activity relationships , 1985, Biopolymers.
[17] M. Goodman,et al. Peptide sweeteners. 6. Structural studies on the C-terminal amino acid of L-aspartyl dipeptide sweeteners. , 1984, Journal of medicinal chemistry.
[18] Olga Kennard,et al. The geometry of the N–H⋯O=C hydrogen bond. 3. Hydrogen-bond distances and angles , 1984 .
[19] P. Balaram,et al. Conformationally constrained chemotactic peptide analogs of high biological activity , 1984, FEBS letters.
[20] H. Scheraga,et al. Energy parameters in polypeptides. 9. Updating of geometrical parameters, nonbonded interactions, and hydrogen bond interactions for the naturally occurring amino acids , 1983 .
[21] V. Hruby,et al. Conformational and dynamic considerations in the design of peptide hormone analogs , 1983, Biopolymers.
[22] H. Nagasawa,et al. Drug latentiation by gamma-glutamyl transpeptidase. , 1982, Journal of medicinal chemistry.
[23] Claudio Toniolo,et al. Linear oligopeptides. 81. Solid-state and solution conformation of homooligo(.alpha.-aminoisobutyric acids) from tripeptide to pentapeptide: evidence for a 310 helix , 1982 .
[24] S. Chládek,et al. Inhibition of the peptidyltransferase acceptor site by 2'(3')-O-cycloleucyl- and alpha-aminoisobutyryl derivatives of cytidylyl-(3'-5')adenosine. , 1982, Biochimica et biophysica acta.
[25] P. Balaram,et al. Hydrophobic channels in crystals of an α-aminoisobutyric acid pentapeptide , 1981 .
[26] Harold A. Scheraga,et al. Sensitivity of polypeptide conformation to geometry. Theoretical conformational analysis of oligomers of .alpha.-aminoisobutyric acid , 1981 .
[27] J. A. Radding,et al. Further studies on the structural requirements for synthetic peptide chemoattractants. , 1980, Biochemistry.
[28] G. Marshall,et al. Interaction of glutathione analogues with Hydra attenuata γ-glutamyltransferase , 1978 .
[29] 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 .
[30] D. Regoli,et al. Synthesis of peptides with the solid phase method. II. Octapeptide analogues of angiotensin II. , 1974, Canadian journal of biochemistry.
[31] R. Zand,et al. Studies in molecular structure, symmetry and conformation VI. Crystal and molecular structure of 1-aminocyclopentane carboxylic acid monohydrate , 1972 .
[32] P. Main,et al. The application of phase relationships to complex structures. III. The optimum use of phase relationships , 1971 .
[33] I. C. O. B. Nomenclature. IUPAC-IUB Commission on Biochemical Nomenclature. Abbreviations and symbols for the description of the conformation of polypeptide chains. Tentative rules (1969). , 1970, Biochemistry.
[34] C. Venkatachalam. Stereochemical criteria for polypeptides and proteins. V. Conformation of a system of three linked peptide units , 1968, Biopolymers.
[35] William C. Davidon,et al. Variance Algorithm for Minimization , 1968, Comput. J..
[36] N. Grant,et al. Peptide Synthesis from N-Carboxy-α-amino Acid Anhydrides in Water. Aminoacylpenicillanic Acids , 1964 .
[37] Roger Fletcher,et al. A Rapidly Convergent Descent Method for Minimization , 1963, Comput. J..
[38] James B. Hendrickson,et al. Molecular Geometry. I. Machine Computation of the Common Rings , 1961 .
[39] G. Rose,et al. Turns in peptides and proteins. , 1985, Advances in protein chemistry.
[40] C. Toniolo,et al. Intramolecularly hydrogen-bonded peptide conformations. , 1980, CRC critical reviews in biochemistry.
[41] P. Balaram,et al. The 310 helical conformation of a pentapeptide containing a-aminoisobutyric acid (Aib): X-ray crystal structure of Tos-(Aib)5 OMe , 1978 .
[42] H. Scheraga,et al. Conformational analysis of the 20 naturally occurring amino acid residues using ECEPP. , 1977, Macromolecules.
[43] I. D. Brown,et al. On the geometry of O–H⋯O hydrogen bonds , 1976 .