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Volumn 131, Issue 21, 2009, Pages 7244-7246

Nature of amide carbonyl-carbonyl interactions in proteins

Author keywords

[No Author keywords available]

Indexed keywords

[CARBONYL; AB INITIO CALCULATIONS; AMIDE BOND; ANTIBONDING ORBITAL; BIOMOLECULAR STRUCTURES; CARBONYL GROUPS; CHEMICAL SUBSTITUENTS; CONFORMATIONAL STABILITIES; DELOCALIZATION; DIPOLE DIPOLE INTERACTIONS; ELECTRONIC DELOCALIZATION; ISOSTERIC; LONE PAIR; MEDICINAL CHEMISTRY; MODEL SYSTEM; NMR SPECTROSCOPY; NON-COVALENT INTERACTION; PEPTIDE BONDS; PROTEIN SECONDARY STRUCTURE; PROTEIN-LIGAND INTERACTIONS; SHORT CONTACTS;

EID: 67650547528     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja901188y     Document Type: Article
Times cited : (243)

References (48)
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    • For textbook descriptions of the Bürgi-Dunitz trajectory, see: Wiley Interscience Publication: New York
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    • Eliel, E.L.1    Wilen, S.H.2
  • 36
    • 0026832808 scopus 로고
    • We chose a methyl ester rather than an amide to avoid the complications of γ-turn formation, as has been observed in AcProNHMe. See: and references therein
    • We chose a methyl ester rather than an amide to avoid the complications of γ-turn formation, as has been observed in AcProNHMe. See: Liang, G.-B.; Rito, C. J.; Gellman, S. H. Biopolymers 1992, 32, 293-301 and references therein.
    • (1992) Biopolymers , vol.32 , pp. 293-301
    • Liang, G.-B.1    Rito, C.J.2    Gellman, S.H.3
  • 40
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    • Similar pyramidalization has been observed to result from an apparent π→π* interaction between an alkene (which lacks any dipole) and a carbonyl group
    • Similar pyramidalization has been observed to result from an apparent π→π* interaction between an alkene (which lacks any dipole) and a carbonyl group. Lloyd, B. A.; Ericson, C.; Arif, A. M.; Allred, E. L. Acta Crystallogr. 1993, C49, 257-261.
    • (1993) Acta Crystallogr. , vol.C49 , pp. 257-261
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  • 41
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.