Structural versatility of peptides from Cα,α-disubstituted glycines: Crystal-state conformational analysis of peptides from Cα-methylhomophenylalanine, (aMe)Hph

International Journal of Peptide and Protein Research

Volumn 47, Issue 6, 1996, Pages 491-497

  Doi, Mitsunobu ^a   Ishida, Toshimasa ^a   Polese, Alessandra ^b   Formaggio, Fernando ^b   Crisma, Marco ^b   Toniolo, Claudio ^b   Broxterman, Quirinus B ^c   Kamphuis, Johan ^c  

^a OSAKA MEDICAL COLLEGE   (Japan)

^b UNIVERSITY OF PADOVA   (Italy)

^c DSM RESEARCH   (Netherlands)

Author keywords

310 helix; Conformational analysis; Crystal structure; C methyl homophenylalanine; Homophenylalanine; Peptide conformation; bend

Indexed keywords

GLYCINE;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; CRYSTAL STRUCTURE; HYDROGEN BOND; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN STRUCTURE; X RAY DIFFRACTION;

AMINOBUTYRIC ACIDS; CRYSTALLOGRAPHY, X-RAY; GLYCINE; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PEPTIDES; PHENYLALANINE; PROTEIN STRUCTURE, SECONDARY;

EID: 0029759624     PISSN: 03678377     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1996.tb01100.x     Document Type: Article

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