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Volumn 127, Issue 24, 2005, Pages 8856-8864

Divergent mechanisms of suicide inactivation for ethanolamine ammonia-lyase

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; ACTIVATION ANALYSIS; ALDEHYDES; AMINES; AMMONIA; DEGRADATION; SUBSTRATES;

EID: 20944437413     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja051527k     Document Type: Article
Times cited : (21)

References (60)
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    • and references therein
    • Indeed, many theoretical investigations of enzyme-catalyzed reactions have successfully approximated the active site with a dielectric of 4.0. See. for example: Himo, F.; Siegbahn, P. E. M. Chem. Rev. 2003, 103, 2421-2456, and references therein.
    • (2003) Chem. Rev. , vol.103 , pp. 2421-2456
    • Himo, F.1    Siegbahn, P.E.M.2
  • 43
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    • Gaussian, Inc.: Pittsburgh, PA
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    • note
    • MOLPRO 2002.6 is a package of ab initio programs written by Werner, H.-J.; et al.
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    • note
    • Although we have generally used protonated forms of the substrates and substrate analogues in all the reaction schemes examined throughout this paper, we have omitted the "protonated" designation within the text for simplicity. However, the nature of the various species is given fully within the schemes.
  • 54
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    • note
    • -1 with PCM).
  • 55
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    • note
    • + from 12.
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    • note
    • 12-dependent enzyme diol dehydratase contain carboxylic acid functional groups. It would be intriguing to see if there were similar consequences to the EAL situation, i.e., production of 4′,5′-anhydroadenosine and degradation of the cofactor, if an inactivator were used with DDH that included or produced a carboxylic acid.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.