Structural and biological evaluation of some loloatin C analogues.

[1]  M. Howard,et al.  Comparison of the effects of 2,2,2-trifluoroethanol on peptide and protein structure and function. , 2007, Journal of structural biology.

[2]  H. Overkleeft,et al.  Beta-turn modified gramicidin S analogues containing arylated sugar amino acids display antimicrobial and hemolytic activity comparable to the natural product. , 2006, Journal of the American Chemical Society.

[3]  G. Siegal,et al.  Conformational Analysis of Furanoid ε-Sugar Amino Acid Containing Cyclic Peptides by NMR Spectroscopy, Molecular Dynamics Simulation, and X-ray Crystallography: Evidence for a Novel Turn Structure , 2003 .

[4]  Jeremy C. Smith,et al.  Molecular Dynamics Simulation of the Cyclic Decapeptide Antibiotic, Gramicidin S, in Dimethyl Sulfoxide Solution , 1999 .

[5]  F. Richards,et al.  The chemical shift index: a fast and simple method for the assignment of protein secondary structure through NMR spectroscopy. , 1992, Biochemistry.

[6]  K. Wüthrich.  NMR of proteins and nucleic acids , 1988 .

[7]  Sunney I. Chan,et al.  Intramolecular hydrogen bonding in gramicidin S. 2. Ornithine , 1982 .

[8]  C. Jones,et al.  Multiple solution conformations and internal rotations of the decapeptide gramicidin S. , 1979, Journal of Biological Chemistry.

[9]  E. Kaiser,et al.  Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. , 1970, Analytical biochemistry.

[10]  R. Andersen,et al.  Loloatins A-D, cyclic decapeptide antibiotics produced in culture by a tropical marine bacterium. , 1999, Journal of natural products.