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Volumn 3, Issue 12, 2012, Pages 3409-3420

Nucleophilic reactivity of Zinc-bound thiolates: Subtle interplay between coordination set and conformational flexibility

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION PARAMETER; CONFORMATIONAL BEHAVIOR; CONFORMATIONAL FLEXIBILITY; COORDINATION PROPERTIES; ELECTROPHILES; ENTHALPY OF ACTIVATION; MODEL PEPTIDES; NEGATIVE ENTROPIES; NEW MEMBERS; NUCLEOPHILIC REACTION; NUCLEOPHILIC REACTIVITY; PHYSIOLOGICAL FUNCTIONS; STRUCTURAL BEHAVIORS; STRUCTURAL CLASS; THERAPEUTIC AGENTS; THIOLATES; TRANSFER REACTION; ZINC FINGER;

EID: 84868087363     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c2sc21029k     Document Type: Article
Times cited : (15)

References (94)
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    • O. Sénèque E. Bonnet F. L. Joumas J. M. Latour Chem.-Eur. J. 2009 15 4798 4810
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  • 83
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    • Yale University Press, New Haven, CT, The final product with the +46 mass increase could also incorporate a sulfinic acid and a thiosulfinate. This was ruled out by reduction with TCEP which led a peptide with a +48 mass increase compared to the fully reduced peptide, thereby proving that the final oxidation corresponds to the oxidation of the sulfinic acid into the sulfonic acid rather than the oxidation of the disulfide into a thiosulfinate
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    • Similar solvation effects have already been invoked for zinc fingers in order to explain changes in entropy that are contrary to the changes in configurational entropy inferred by NMR. See
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.