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ACS Chem Biol ; 12(10): 2535-2537, 2017 10 20.
Article in English | MEDLINE | ID: mdl-28886246

ABSTRACT

Anions have long been known to engage in stabilizing interactions with electron-deficient arenes. However, the precise nature and energetic contribution of anion-π interactions to protein stability remains a subject of debate. Here, we show that placing a negatively charged Asp in close proximity to electron-rich Phe in a reverse turn within the WW domain results in a favorable interaction that increases WW conformational stability by -1.3 kcal/mol.


Subject(s)
Amino Acids/chemistry , NIMA-Interacting Peptidylprolyl Isomerase/chemistry , Amino Acid Sequence , Models, Molecular , Protein Conformation, beta-Strand , Protein Domains
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