An Easy Entry to a New High-Symmetry, Large Molecular Framework for Molecular Recognition Studies and de Novo Protein Design. Solvent Modulation of the Spontaneous Formation of a Cyclic Monomer, Dimer, or Trimer from a Bis-cysteine Peptide
- 13 June 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (27) , 6639-6650
- https://doi.org/10.1021/ja9725514
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- The Alacoil: A very tight, antiparallel coiled‐coil of helicesProtein Science, 1995
- Structural analysis of the N‐ and C‐termini in a peptide with consensus sequenceProtein Science, 1995
- Helix propensities of the amino acids measured in alanine‐based peptides without helix‐stabilizing side‐chain interactionsProtein Science, 1994
- Design of a heme-binding four-helix bundleJournal of the American Chemical Society, 1994
- NMR chemical shifts: a tool to characterize distortions of peptide and protein helicesJournal of the American Chemical Society, 1992
- 13C-{1H} NMR/NOE and multiplet relaxation data in modeling protein dynamics of a collagen 13C-enriched glycine GXX repeat motif hexadecapeptideJournal of the American Chemical Society, 1992
- Use of the Npys thiol protection in solid phase peptide synthesis Application to direct peptide‐protein conjugation through cysteine residuesInternational Journal of Peptide and Protein Research, 1989
- General architecture of the α-helical globuleJournal of Molecular Biology, 1988
- Preparation of Boc‐[S‐(3‐nitro‐2‐pyridinesulfenyl)]‐cysteine and its use for unsymmetrical disulfide bond formationInternational Journal of Peptide and Protein Research, 1986
- Conformational aspects of polypeptides. XI. The nitroaromatic effectBiopolymers, 1963