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- W1995535745 endingPage "13264" @default.
- W1995535745 startingPage "13257" @default.
- W1995535745 abstract "Ab initio calculations are used to compare the abilities of the aromatic groups of the Phe, Tyr, Trp, and His amino acids (modeled respectively by benzene, phenol, indole, and imidazole) to form H-bonds of three different types. Strongest of all are the conventional H-bonds (e.g., OH··O and OH··N). His forms the strongest such H-bond, followed by Tyr, and then by Trp. Whereas OH··φ bonds formed by the approach of a proton donor to the π electron cloud above the aromatic system are somewhat weaker, they nonetheless represent an important class of stabilizing interactions. The strengths of H-bonds in this category follow the trend Trp > His > Tyr ∼ Phe. CH··O interactions are weaker still, and only those involving His and Trp are strong enough to make significant contributions to protein structure. A protonated residue such as HisH+ makes for a very powerful proton donor, such that even its CH··O H-bonds are stronger than the conventional H-bonds formed by neutral groups." @default.
- W1995535745 created "2016-06-24" @default.
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- W1995535745 creator A5047327365 @default.
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- W1995535745 date "2002-10-15" @default.
- W1995535745 modified "2023-10-16" @default.
- W1995535745 title "Comparison of Various Types of Hydrogen Bonds Involving Aromatic Amino Acids" @default.
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- W1995535745 doi "https://doi.org/10.1021/ja027200q" @default.
- W1995535745 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12405854" @default.
- W1995535745 hasPublicationYear "2002" @default.
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