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Impact of azaproline on peptide conformation
Ye Che
, Garland R. Marshall
Department of Biochemistry & Molecular Biophysics
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
Institute of Clinical and Translational Sciences (ICTS)
Research output
:
Contribution to journal
›
Article
›
peer-review
54
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Scopus citations
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Keyphrases
Peptide Conformation
100%
Azaproline
100%
Cis-amide
63%
Amides
36%
Conformational Preferences
27%
Amide Bond
18%
Cis-trans Isomerization
18%
Pipecolic Acid
18%
Acetyl
18%
Side Chain
9%
Methyl
9%
Water Molecule
9%
Hydrogen Bonds (H-bonds)
9%
Proline
9%
Isomerization
9%
Organic Solvents
9%
Conformational Constraint
9%
Solvation Effect
9%
Aqueous Solution
9%
Peptide Backbone
9%
Chemical Modification
9%
Reverse Turns
9%
Acyl
9%
Enhanced Stability
9%
Amino Acid Analogs
9%
Bioactive Peptides
9%
Nitrogen Atom
9%
Pyrrolidine
9%
Energy Barrier
9%
Intramolecular Hydrogen Bond
9%
G-levels
9%
In Vacuo
9%
Large Rings
9%
Ab Initio Study
9%
Steric Bulk
9%
Biological Recognition
9%
Nme2
9%
Internal Hydrogen
9%
Polarizable Continuum Model
9%
Pyrazolidines
9%
Lone Pair
9%
Chemistry
Carboxamide
100%
Conformational Isomer
90%
Hydrogen Bonding
18%
Acetyl
18%
Pipecolic Acid
18%
NMR Spectroscopy
9%
Solvation
9%
Reverse Turn
9%
Cis-Trans Isomerism
9%
Nitrogen Atom
9%
Møller-Plesset Perturbation Theory
9%
Energy Barrier
9%
Pyrazolidine
9%
Amino Acid
9%
Aqueous Solution
9%
Proline
9%
Pyrrolidine
9%
Isomerization
9%