A computergraphic determination of the chemotactic peptide preferred conformation
- 1 December 1988
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 157 (2) , 569-574
- https://doi.org/10.1016/s0006-291x(88)80287-0
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Strategic approaches to drug design. I. An integrated software framework for molecular modellingJournal of Computer-Aided Molecular Design, 1987
- A highly active chemotactic peptide analog incorporating the unusual residue 1-aminocyclohexanecarboxylic acid at position 2Biochemical and Biophysical Research Communications, 1985
- Structural requirements for formyl homooligopeptide chemoattractantsBiochemistry, 1984
- Conformationally constrained chemotactic peptide analogs of high biological activityFEBS Letters, 1984
- Preferred conformations of peptides containing α,α‐disubstituted α‐amino acidsBiopolymers, 1983
- Formyl peptide chemoattractants: a model of the receptor on rabbit neutrophilsBiochemistry, 1982
- Further studies on the structural requirements for synthetic peptide chemoattractantsBiochemistry, 1980
- Nuclear magnetic resonance conformational studies on the chemotactic tripeptide formyl-L-methionyl-L-leucyl-L-phenylalanine. A small .beta. sheetBiochemistry, 1979
- The structure-activity relations of synthetic peptides as chemotactic factors and inducers of lysosomal secretion for neutrophils.The Journal of Experimental Medicine, 1976
- 1161. Peptides. Part XVIII. Derivatives of 1-aminocyclohexanecarboxylic acidJournal of the Chemical Society, 1965