n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
about
n-->pi* interactions in proteinsAtomic polarizability dominates the electronic properties of peptide bonds upon thioxo or selenoxo substitution.IMPIPS: the immune protection-inducing protein structure concept in the search for steric-electron and topochemical principles for complete fully-protective chemically synthesised vaccine developmentElectronic and Steric Optimization of Fluorogenic Probes for Biomolecular ImagingThe aberrance of the 4S diastereomer of 4-hydroxyproline.Catalytic site-selective thiocarbonylations and deoxygenations of vancomycin reveal hydroxyl-dependent conformational effects.A Single Stereodynamic Center Modulates the Rate of Self-Assembly in a Biomolecular System.Origins of stereoselectivities of dihydroxylations of cis-bicyclo[3.3.0]octenesProlyl 4-Hydroxylase: Substrate Isosteres in Which an (E)- or (Z)-Alkene Replaces the Prolyl Peptide Bond.Diversity of Secondary Structure in Catalytic Peptides with β-Turn-Biased SequencesAn evaluation of peptide-bond isosteres.The n → π* interaction: a rapidly emerging non-covalent interaction.An n→π* interaction in aspirin: implications for structure and reactivity.Pyramidalization of a carbonyl C atom in (2S)-N-(seleno-acet-yl)proline methyl ester.4-Fluoroprolines: Conformational Analysis and Effects on the Stability and Folding of Peptides and Proteins.The n→π* InteractionIntimate interactions with carbonyl groups: dipole-dipole or n→π*?n→π* interactions engender chirality in carbonyl groupsAn n→π* interaction reduces the electrophilicity of the acceptor carbonyl group.Signature of n→π* interactions in α-helices.Signatures of n→π* interactions in proteins.A conserved interaction with the chromophore of fluorescent proteins.A key n→π* Interaction in N-acyl homoserine lactones.Palladium-Catalyzed Defluorinative Coupling of 1-Aryl-2,2-Difluoroalkenes and Boronic Acids: Stereoselective Synthesis of Monofluorostilbenes.n→π* interactions of amides and thioamides: implications for protein stability.n→π* interactions in poly(lactic acid) suggest a role in protein folding.Natural bond orbital analysis in the ONETEP code: applications to large protein systems.Peptide Solubility Limits: Backbone and Side-Chain Interactions.Synthesis and Deployment of an Elusive Fluorovinyl Cation Equivalent: Access to Quaternary α-(1'-Fluoro)vinyl Amino Acids as Potential PLP Enzyme Inactivators.Manganese-catalyzed synthesis of monofluoroalkenes via C-H activation and C-F cleavage.Visible light photocatalytic decarboxylative monofluoroalkenylation of α-amino acids with gem-difluoroalkenes.Stereospecific Synthesis of Fluoroalkenes by Silver-Mediated Fluorination of Functionalized Alkenylstannanes.Comparison of P···D (D = P,N) with other noncovalent bonds in molecular aggregates.Peptoid conformational free energy landscapes from implicit-solvent molecular simulations in AMBER.Modulation of an n→π* interaction with α-fluoro groupsSynthesis of novel enantiomerically pure tetra-carbohydrazide cyclophane macrocycles
P2860
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P2860
n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
@en
type
label
n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
@en
prefLabel
n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
@en
P2860
P356
P1476
n --> pi* Interaction and n)(pi Pauli repulsion are antagonistic for protein stability.
@en
P2093
Amit Choudhary
Charles E Jakobsche
P2860
P304
P356
10.1021/JA100931Y
P407
P577
2010-05-01T00:00:00Z