Peptide models XXVII. An exploratory ab initio study on the 21st amino acid side-chain conformations of N-formyl-L-selenocysteinamide (For-L-Sec- NH2) and N-acetyl-L-selenocysteine-N-methylamide (Ac-L-Sec-NHMe) in their γ(L) backbone conformation

Canadian Journal of Chemistry

Volumn 78, Issue 3, 2000, Pages 395-408

  Vank, Judith C ^a   Sosa, Carlos P ^b   Perczel, Andras ^c,d   Csizmadia, Imre G ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b HEWLETT PACKARD ENTERPRISE   (United States)

^c EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^d UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Ab initio MO study; Atoms in Molecules (AIM); Bader's electron density analysis; Multidimensional Conformational Analysis (MDCA); Selenocysteine side chain conformations

Indexed keywords

SELENOCYSTEINE;

ARTICLE; CHEMICAL ANALYSIS; ELECTRON TRANSPORT; MOLECULAR BIOLOGY; PEPTIDE ANALYSIS; PROTEIN CONFORMATION; THEORY;

EID: 0034014622     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/cjc-78-3-395     Document Type: Article

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