Solution state conformation and degradation of cyclopeptides containing an NGR motif

Journal of Peptide Science

Volumn 11, Issue 1, 2005, Pages 53-59

  Füzéry, Anna K ^a   Mihala, Nikolett ^b   Szabó, Pál ^c   Perczel, András ^a   Giavazzi, Raffaella ^d   Süli Vargha, Helga ^b,e  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^c CHEMICAL RESEARCH CENTER   (Hungary)

^d MARIO NEGRI INST PHARMACOL RES   (Italy)

^e NONE   (Hungary)

Author keywords

Adhesion; Cyclopeptide; Deamidation; Integrin receptor; MD and ab initio calculation; NGR; NMR conformation

Indexed keywords

ASPARAGINE; CYCLOPEPTIDE; GLYCINE; INTEGRIN RECEPTOR; VERY LATE ACTIVATION ANTIGEN 5;

AMINO ACID SEQUENCE; ANGIOGENESIS; ARTICLE; CELL ADHESION; CYCLIZATION; DEAMINATION; ENDOTHELIUM CELL; EXTRACELLULAR MATRIX; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; IN VIVO STUDY; MASS SPECTROMETRY; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE; PEPTIDE SYNTHESIS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN HYDROLYSIS; PROTEIN MOTIF; PROTEIN PURIFICATION; PROTEIN STRUCTURE; PROTEIN TARGETING; RECEPTOR AFFINITY;

AMINO ACID MOTIFS; ARGININE; ASPARAGINE; CELL ADHESION; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ENDOTHELIUM, VASCULAR; GLYCINE; HUMANS; INTEGRINS; MAGNETIC RESONANCE SPECTROSCOPY; PEPTIDES, CYCLIC; PROTEIN CONFORMATION; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;

EID: 12144263707     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/psc.588     Document Type: Article

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