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Volumn 7, Issue 6, 2010, Pages 1612-1624

Configurational assignment of D- and L-isovalines in intact, natural, and synthetic peptides by 2D-NMR spectroscopy

(8) De Zotti, Marta a Schievano, Elisabetta a Mammi, Stefano a Kaptein, Bernard b Broxterman, Quirinus B b Singh, Sheo B c Brückner, Hans d Toniolo, Claudio a

a UNIVERSITY OF PADOVA (Italy)

b DSM RESOLVE (Netherlands)

c MERCK RESEARCH LABORATORIES (United States)

d JUSTUS LIEBIG UNIVERSITY (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTIC ACID; HYDROGEN; ISOVALINE; LEUCINE; SYNTHETIC PEPTIDE; TETRAPEPTIDE; INTEGRAMIDE A; INTEGRAMIDE B; OLIGOPEPTIDE; VALINE;

AMINO ACID ANALYSIS; ARTICLE; ATOM; DIASTEREOISOMER; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; AMINO ACID SEQUENCE; CHEMISTRY; CIRCULAR DICHROISM; MOLECULAR GENETICS; PROTEIN SECONDARY STRUCTURE; STEREOISOMERISM;

IVA;

AMINO ACID SEQUENCE; CIRCULAR DICHROISM; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR SEQUENCE DATA; OLIGOPEPTIDES; PROTEIN STRUCTURE, SECONDARY; STEREOISOMERISM; VALINE;

EID: 77953891989 PISSN: 16121872 EISSN: 16121880 Source Type: Journal
DOI: 10.1002/cbdv.200900287 Document Type: Article

Times cited : (10)

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