Conformational energy analysis of the chemotactic tripeptide formyl-Met-Leu-Phe and three analogs
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1989.tb00235.x/fullpdf
Reference22 articles.
1. N-formylmethionyl peptides as chemoattractants for leucocytes.
2. The structure-activity relations of synthetic peptides as chemotactic factors and inducers of lysosomal secretion for neutrophils.
3. SYNTHESIS OF Nα-FORMYL-MET-LEU-PHE-OH: AN INDUCER OF CHEMOTAXIS IN PERITONEAL POLYMORPHONUCLEAR NEUTROPHILS
4. Nuclear magnetic resonance conformational studies on the chemotactic tripeptide formyl-L-methionyl-L-leucyl-L-phenylalanine. A small .beta. sheet
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1. Synthesis, biological activity, conformational analysis by NMR and molecular modeling of N-formyl-L-Met-L-Pro-L-Phe-OMe, a praline analogue of the chemotactic peptide N-formyl-L-Met-L-Leu-L-Phe-OH;International Journal of Peptide and Protein Research;2009-01-12
2. Synthesis and properties of chemotactic peptide analogs I. Crystal structure and molecular conformation of HCO-Met-Leu-Ain-OMe;International Journal of Peptide and Protein Research;2009-01-12
3. Conformational investigations on analogs of inflammation response inducing chemotactic tripeptide fMLP;Biopolymers;2005
4. Multiple domains of the N-formyl peptide receptor are required for high-affinity ligand binding. Construction and analysis of chimeric N-formyl peptide receptors.;Journal of Biological Chemistry;1993-08
5. Role of peptide backbone conformation on biological activity of chemotactic peptides.;Journal of Biological Chemistry;1991-10
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