Carboxy-terminal extension stabilizes the topological stereoisomers of guanylin

Journal of Peptide Research

Volumn 52, Issue 6, 1998, Pages 518-525

  Schulz, A ^a   Escher, S ^a   Marx, U C ^a,b   Meyer, M ^a   Rosch P ^b   Forssmann, W G ^a   Adermann, Knut ^a  

^a IPF PHARMACEUTICALS GMBH   (Germany)

^b UNIVERSITY OF BAYREUTH   (Germany)

Author keywords

Guanylin; Guanylyl cyclase C; NMR; Structure; Topological stereoisomer

Indexed keywords

AMINO ACID; CYCLIC GMP; CYSTEINE; GUANYLATE CYCLASE; GUANYLIN; LEUCINE; TYROSINE; UROGUANYLIN;

AMIDATION; AMINO ACID SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; ISOMER; ISOMERISM; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RADIOIMMUNOASSAY; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; STEREOISOMERISM;

EID: 0032417733     PISSN: 1397002X     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1998.tb01256.x     Document Type: Article

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