about
Signal Transduction in Receptor for Advanced Glycation End Products (RAGE): SOLUTION STRUCTURE OF C-TERMINAL RAGE (ctRAGE) AND ITS BINDING TO mDia1Conformational restriction through C alpha i C alpha i cyclization: Ac12c, the largest cycloaliphatic C alpha,alpha- disubstituted glycine knownA prevalent intraresidue hydrogen bond stabilizes proteins.Water mediation is essential to nucleation of β-turn formation in peptide folding motifs.Secondary structures of short peptide chains in the gas phase: double resonance spectroscopy of protected dipeptides.Investigation of the interaction between the atypical agonist c[YpwFG] and MOR.Preferred conformation of peptides based on cycloaliphatic C(alpha,alpha)-disubstituted glycines: 1-amino-cycloundecane-1-carboxylic acid (Ac11c).Control of peptide conformation by the Thorpe-Ingold effect (C alpha-tetrasubstitution).Computational survey of peptides derived from disulphide-bonded protein loops that may serve as mediators of protein-protein interactionsStructural characterization of triple transmembrane domain containing fragments of a yeast G protein-coupled receptor in an organic : aqueous environment by solution-state NMR spectroscopyLong polypeptide 3(10)-helices at atomic resolution.Novel disulfide-constrained pentapeptides as models for beta-VIa turns in proteins.A novel secondary structure based on fused five-membered rings motifToward a Rational Design of Highly Folded Peptide Cation Conformations. 3D Gas-Phase Ion Structures and Ion Mobility Characterization.Handedness preference and switching of peptide helices. Part I: Helices based on protein amino acids.Handedness preference and switching of peptide helices. Part II: Helices based on noncoded α-amino acids.Structure-Based Design of Inhibitors of Protein-Protein Interactions: Mimicking Peptide Binding Epitopes.Conformation, self-aggregation, and membrane interaction of peptaibols as studied by pulsed electron double resonance spectroscopy.Intramolecular backbone···backbone hydrogen bonds in polypeptide conformations. The other way around: ɛ-turn.En route towards the peptide γ-helix: X-ray diffraction analyses and conformational energy calculations of Adm-rich short peptides.Multifactorial level of extremostability of proteins: can they be exploited for protein engineering?Peptide δ-Turn: Literature Survey and Recent Progress.X-ray crystallography of peptides: the contributions of the Italian laboratories.In-peptide synthesis of di-oxazolidinone and dehydroamino acid-oxazolidinone motifs as β-turn inducers.Effects of hydrogen-bond deletion on peptide helices: structural characterization of depsipeptides containing lactic acid.C(alpha)-hydroxymethyl methionine: synthesis, optical resolution and crystal structure of its (+)-N(alpha)-benzoyl derivative.Nitroxyl peptides as catalysts of enantioselective oxidations.β-turn tendency in N-methylated peptides with dehydrophenylalanine residue: DFT study.Peptoid residues and beta-turn formation.Multiple, consecutive, fully-extended 2.0₅-helix peptide conformation.Folding of peptides characterized by c3Val, a highly constrained analogue of valine.N-benzhydryl-glycolamide: the first protecting group in peptide synthesis with a strong conformational bias.New tools for the control of peptide conformation and supramolecular chemistry: crown-carrier, C(alpha)-methyl L-DOPA amino acids.New tools for the control of peptide conformation: the helicogenic Calpha-methyl, Calpha-cyclohexylglycine.Thionoglycine as a multifunctional spectroscopic reporter of screw-sense preference in helical foldamers.Solution synthesis, conformational analysis, and antimicrobial activity of three alamethicin F50/5 analogs bearing a trifluoroacetyl label.The 2.0₅-helix in hetero-oligopeptides entirely composed of C(α,α)-disubstituted glycines with both side chains longer than methyls.Conformational properties, membrane interaction, and antibacterial activity of the peptaibiotic chalciporin A: Multitechnique spectroscopic and biophysical investigations on the natural compound and labeled analogs.Synthesis and conformational properties of a TOAC doubly spin-labeled analog of the medium-length, membrane active peptaibiotic ampullosporin A as revealed by CD, fluorescence, and EPR spectroscopies.α-Aminoxy Peptoids: A Unique Peptoid Backbone with a Preference for cis-Amide Bonds.
P2860
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P2860
description
1980 nî lūn-bûn
@nan
1980 թուականին հրատարակուած գիտական յօդուած
@hyw
1980 թվականին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
Intramolecularly hydrogen-bonded peptide conformations
@ast
Intramolecularly hydrogen-bonded peptide conformations
@en
Intramolecularly hydrogen-bonded peptide conformations
@nl
type
label
Intramolecularly hydrogen-bonded peptide conformations
@ast
Intramolecularly hydrogen-bonded peptide conformations
@en
Intramolecularly hydrogen-bonded peptide conformations
@nl
prefLabel
Intramolecularly hydrogen-bonded peptide conformations
@ast
Intramolecularly hydrogen-bonded peptide conformations
@en
Intramolecularly hydrogen-bonded peptide conformations
@nl
P2860
P3181
P1476
Intramolecularly hydrogen-bonded peptide conformations
@en
P2093
P2860
P3181
P356
10.3109/10409238009105471
P407
P577
1980-01-01T00:00:00Z