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  Stereochemistry and accessibility of prosthetic groups in flavoproteins

Manstein, D. J., Massey, V., Ghisla, S., & Pai, E. F. (1988). Stereochemistry and accessibility of prosthetic groups in flavoproteins. Biochemistry, 27(7), 2300-2305. doi:10.1021/bi00407a009.

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 Creators:
Manstein, Dietmar J.1, Author           
Massey, Vincent, Author
Ghisla, Sandro, Author
Pai, Emil F., Author
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1Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society, ou_1497712              

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 Abstract: Using 8-demethyl-8-hydroxy-5-deaza-5-carba analogues of the appropriate flavin nucleotides, we determined the stereochemistry of interaction between coenzyme and substrate for several flavoproteins. The enzymes were D-amino acid oxidase, L-lactate oxidase, and D-lactate dehydrogenase, all three of which interact with pyruvate, as well as cyclohexanone monooxygenase and 2-methyl-3-hydroxypyridine-5-carboxylic acid oxygenase, which were both probed with nicotinamide nucleotides. L-Lactate oxidase and D-lactate dehydrogenase used the si face of the modified flavin ring while the other three enzymes showed re-side specificity. This selection of flavoenzymes includes FAD- and FMN-dependent enzymes, enzymes that follow a carbanion mechanism, and others that have hydride transfer as an integral part of their reaction pathway.

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Language(s): eng - English
 Dates: 1988-04-05
 Publication Status: Issued
 Pages: 6
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 Rev. Type: Peer
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Title: Biochemistry
Source Genre: Journal
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Publ. Info: Columbus, Ohio : American Chemical Society
Pages: - Volume / Issue: 27 (7) Sequence Number: - Start / End Page: 2300 - 2305 Identifier: ISSN: 0006-2960
CoNE: https://pure.mpg.de/cone/journals/resource/954925384103