Literature DB >> 10966480

Swinging arms and swinging domains in multifunctional enzymes: catalytic machines for multistep reactions.

R N Perham1.   

Abstract

Multistep chemical reactions are increasingly seen as important in a growing number of complex biotransformations. Covalently attached prosthetic groups or swinging arms, and their associated protein domains, are essential to the mechanisms of active-site coupling and substrate channeling in a number of the multifunctional enzyme systems responsible. The protein domains, for which the posttranslational machinery in the cell is highly specific, are crucially important, contributing to the processes of molecular recognition that define and protect the substrates and the catalytic intermediates. The domains have novel folds and move by virtue of conformationally flexible linker regions that tether them to other components of their respective multienzyme complexes. Structural and mechanistic imperatives are becoming apparent as the assembly pathways and the coupling of multistep reactions catalyzed by these dauntingly complex molecular machines are unraveled.

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Year:  2000        PMID: 10966480     DOI: 10.1146/annurev.biochem.69.1.961

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  165 in total

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5.  Chromosomal amplification of the Escherichia coli lipB region confers high-level resistance to selenolipoic acid.

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8.  The effect of electrostatics on the marginal cooperativity of an ultrafast folding protein.

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9.  The human peripheral subunit-binding domain folds rapidly while overcoming repulsive Coulomb forces.

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Review 10.  Lipoic acid metabolism in microbial pathogens.

Authors:  Maroya D Spalding; Sean T Prigge
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

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