Literature DB >> 28065269

Methods for Structural and Functional Analyses of Intramembrane Prenyltransferases in the UbiA Superfamily.

Y Yang1, N Ke2, S Liu1, W Li3.   

Abstract

The UbiA superfamily is a group of intramembrane prenyltransferases that generate lipophilic compounds essential in biological membranes. These compounds, which include various quinones, hemes, chlorophylls, and vitamin E, participate in electron transport and function as antioxidants, as well as acting as structural lipids of microbial cell walls and membranes. Prenyltransferases producing these compounds are involved in important physiological processes and human diseases. These UbiA superfamily members differ significantly in their enzymatic activities and substrate selectivities. This chapter describes examples of methods that can be used to group these intramembrane enzymes, analyze their activity, and screen and crystallize homolog proteins for structure determination. Recent structures of two archaeal homologs are compared with structures of soluble prenyltransferases to show distinct mechanisms used by the UbiA superfamily to control enzymatic activity in membranes.
© 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  COQ2; Crystal structures; Crystallography; Intramembrane enzymes; Liquid cubic phase; Membrane proteins; Prenyltransferases; Quinones; Sequence clustering; Structural lipids; UBIAD1; UbiA

Mesh:

Substances:

Year:  2016        PMID: 28065269      PMCID: PMC5432130          DOI: 10.1016/bs.mie.2016.10.032

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  88 in total

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Authors:  B Miroux; J E Walker
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Review 6.  Ubiquinone biosynthesis in microorganisms.

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Journal:  FEMS Microbiol Lett       Date:  2001-09-25       Impact factor: 2.742

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10.  Structure of a membrane-embedded prenyltransferase homologous to UBIAD1.

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4.  Construction of a novel MK-4 biosynthetic pathway in Pichia pastoris through heterologous expression of HsUBIAD1.

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