Comparison of various types of hydrogen bonds involving aromatic amino acids.
about
Stabilization and characterization of a heme-oxy reaction intermediate in inducible nitric-oxide synthaseSubstituent effects on non-covalent interactions with aromatic rings: insights from computational chemistrySequential unfolding of the hemolysin two-partner secretion domain from Proteus mirabilis.Mechanisms of proton conduction and gating in influenza M2 proton channels from solid-state NMRAdamantyl-substituted retinoid-derived molecules that interact with the orphan nuclear receptor small heterodimer partner: effects of replacing the 1-adamantyl or hydroxyl group on inhibition of cancer cell growth, induction of cancer cell apoptosisBoltzmann-type distribution of side-chain conformation in proteinsAb initio calculations and validation of the pH-dependent structures of the His37-Trp41 quartet, the heart of acid activation and proton conductance in the M2 protein of Influenza A virusEffects of tryptophan microenvironment, soluble domain, and vesicle size on the thermodynamics of membrane protein folding: lessons from the transmembrane protein OmpA.Architecture of the ATG2B-WDR45 complex and an aromatic Y/HF motif crucial for complex formation.Computational analysis of BACE1-ligand complex crystal structures and linear discriminant analysis for identification of BACE1 inhibitors with anti P-glycoprotein binding property.Structure of Amido Pyridinium Betaines: Persistent Intermolecular C-H⋅⋅⋅N Hydrogen Bonding in Solution.Lone pair ... pi interactions between water oxygens and aromatic residues: quantum chemical studies based on high-resolution protein structures and model compounds.Metal-organic frameworks exhibiting strong anion-pi interactions.Directed evolution of Aspergillus niger glucoamylase to increase thermostability.Solvation and microscopic properties of ionic liquid/acetonitrile mixtures probed by high-pressure infrared spectroscopy.Efficiency of histidine-associating compounds for blocking the alzheimer's Abeta channel activity and cytotoxicity.Coexistence of solvated electron and benzene-centered valence anion in the negatively charged benzene-water clusters.The effect of fluorine substitution on chiral recognition: interplay of CH···π, OH···π and CH···F interactions in gas-phase complexes of 1-aryl-1-ethanol with butan-2-ol.How are hydrogen bonds modified by metal binding?Probing C-H...X hydrogen bonds in amide-functionalized imidazolium salts under high pressure.Substrate-assisted leaving group activation in enzyme-catalyzed N-glycosidic bond cleavage.A novel approach for the design of a highly selective sulfate-ion-selective electrode.A theoretical study of weak interactions in phenylenediamine homodimer clusters.Interpretation of Spectroscopic Markers of Hydrogen Bonds.Orientation-dependent potential of mean force for protein folding.Acetylcholinesterase from the invertebrate Ciona intestinalis is capable of assembling into asymmetric forms when co-expressed with vertebrate collagenic tail peptide.Modulating weak interactions for molecular recognition: a dynamic combinatorial analysis for assessing the contribution of electrostatics to the stability of CH-π bonds in water.Water sandwiched by a pair of aromatic rings in a proton-conducting metal-organic framework.Unexpected solvent effects on the UV/Vis absorption spectra of o-cresol in toluene and benzene: in contrast with non-aromatic solvents.On the non-classical contribution in lone-pair–π interaction: IQA perspective
P2860
Q24655182-91F602C0-343D-4A92-8219-CB719A10DAF1Q28248427-A302C206-E62A-483C-8589-712E57F2CEB8Q30152834-DCDC9064-5F3A-45C9-A8F7-961DD4EB3061Q33725154-335DD040-A4B0-4D26-A1DD-43918222F919Q33900787-4373B034-2C36-470B-9217-A1ED7055E789Q36631481-B875D170-9EB0-48A3-9491-92CC032453DFQ37069593-74B881E6-DC7D-44BB-AF86-16B29AEE1A39Q37299444-59B287E4-7F63-4D66-B286-75C0FE03431FQ38618611-4A35F0BB-4F37-4E78-8C94-BEBDC394C11CQ39024147-777CF880-ADF7-4AE4-9E52-F67F30177A61Q40047581-756074EB-4E3B-43A6-8CE7-FA03D0BC2817Q42581561-787D0EAC-B5DF-4B10-9573-2C2493B93332Q42698040-ABC3C8B3-A704-4BD0-818E-78FAF82C3044Q42924603-5E2C21E2-BED0-4D94-BC2B-4F7EDE6278E0Q43213110-9F346CFC-347E-405E-9910-CA0C8C088FB6Q43248443-55750BC6-A62F-4417-8529-CBB02725140EQ43630255-E00009C6-A437-4312-872F-590A953536C1Q44032559-C46F402E-3827-4E23-BA2F-28DC647F3AA6Q44820577-D67B11C2-081F-47B4-9101-36655A2F99B5Q44988719-D1DB9EF1-6EB0-413E-BA8B-B2961886D7D5Q45254078-D86C5CF2-D870-44EF-ACE1-D61FCF9FB10DQ46125633-A2F8C067-32B0-43FA-8171-16454C7B24C6Q46471211-56B03A9A-19FC-4DB5-B75B-4689EFE742D3Q46569227-32292BCF-02A2-4FA4-85BB-DFBB37D52F5CQ46612116-7289CC55-15B4-40AB-9C3F-9CA3B706EF05Q46750543-910DB0F3-737D-401C-8D3A-E289A8D48581Q51009943-72774601-95B7-460E-8F96-53FE8D56F49CQ51121475-8D9EF920-5008-44BC-9624-2EB7785E7D59Q55196286-1ECF4E66-DDA0-46BF-AB45-A79A90AEFF90Q57744759-F84A3BA6-06DE-4C8A-9D84-097B81B33292
P2860
Comparison of various types of hydrogen bonds involving aromatic amino acids.
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@ast
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@en
type
label
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@ast
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@en
prefLabel
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@ast
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@en
P2093
P356
P1476
Comparison of various types of hydrogen bonds involving aromatic amino acids.
@en
P2093
Jayasree Pattanayak
Steve Scheiner
P304
13257-13264
P356
10.1021/JA027200Q
P407
P577
2002-11-01T00:00:00Z