Literature DB >> 15189147

Pyridoxal phosphate enzymes: mechanistic, structural, and evolutionary considerations.

Andrew C Eliot1, Jack F Kirsch.   

Abstract

Pyridoxal phosphate (PLP)-dependent enzymes are unrivaled in the diversity of reactions that they catalyze. New structural data have paved the way for targeted mutagenesis and mechanistic studies and have provided a framework for interpretation of those results. Together, these complementary approaches yield new insight into function, particularly in understanding the origins of substrate and reaction type specificity. The combination of new sequences and structures enables better reconstruction of their evolutionary heritage and illuminates unrecognized similarities within this diverse group of enzymes. The important metabolic roles of many PLP-dependent enzymes drive efforts to design specific inhibitors, which are now guided by the availability of comprehensive structural and functional databases. Better understanding of the function of this important group of enzymes is crucial not only for inhibitor design, but also for the design of improved protein-based catalysts.

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Year:  2004        PMID: 15189147     DOI: 10.1146/annurev.biochem.73.011303.074021

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


  239 in total

1.  Linkage between the bacterial acid stress and stringent responses: the structure of the inducible lysine decarboxylase.

Authors:  Usheer Kanjee; Irina Gutsche; Eftichia Alexopoulos; Boyu Zhao; Majida El Bakkouri; Guillaume Thibault; Kaiyin Liu; Shaliny Ramachandran; Jamie Snider; Emil F Pai; Walid A Houry
Journal:  EMBO J       Date:  2011-01-28       Impact factor: 11.598

2.  Covalent attachment of pyridoxal-phosphate derivatives to 14-3-3 proteins.

Authors:  Lars Röglin; Philipp Thiel; Oliver Kohlbacher; Christian Ottmann
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-24       Impact factor: 11.205

3.  Overexpression, crystallization and preliminary X-ray crystallographic analysis of pyridoxal biosynthesis lyase PdxS from Pyrococcus horikoshii.

Authors:  Ji Young Yoon; Chan Ryang Park; Hyung Ho Lee; Se Won Suh
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2012-03-27

Review 4.  The structural biology of enzymes involved in natural product glycosylation.

Authors:  Shanteri Singh; George N Phillips; Jon S Thorson
Journal:  Nat Prod Rep       Date:  2012-06-12       Impact factor: 13.423

5.  Inhibition of the PLP-dependent enzyme serine palmitoyltransferase by cycloserine: evidence for a novel decarboxylative mechanism of inactivation.

Authors:  Jonathan Lowther; Beverley A Yard; Kenneth A Johnson; Lester G Carter; Venugopal T Bhat; Marine C C Raman; David J Clarke; Britta Ramakers; Stephen A McMahon; James H Naismith; Dominic J Campopiano
Journal:  Mol Biosyst       Date:  2010-05-05

6.  Characterization of Enzymes Catalyzing Transformations of Cysteine S-Conjugated Intermediates in the Lincosamide Biosynthetic Pathway.

Authors:  Richiro Ushimaru; Chia-I Lin; Eita Sasaki; Hung-Wen Liu
Journal:  Chembiochem       Date:  2016-07-19       Impact factor: 3.164

7.  Structural analysis of QdtB, an aminotransferase required for the biosynthesis of dTDP-3-acetamido-3,6-dideoxy-alpha-D-glucose.

Authors:  James B Thoden; Christina Schäffer; Paul Messner; Hazel M Holden
Journal:  Biochemistry       Date:  2009-02-24       Impact factor: 3.162

8.  Crystal structure of PhnH: an essential component of carbon-phosphorus lyase in Escherichia coli.

Authors:  Melanie A Adams; Yan Luo; Bjarne Hove-Jensen; Shu-Mei He; Laura M van Staalduinen; David L Zechel; Zongchao Jia
Journal:  J Bacteriol       Date:  2007-11-09       Impact factor: 3.490

9.  A chemogenomic screening of sulfanilamide-hypersensitive Saccharomyces cerevisiae mutants uncovers ABZ2, the gene encoding a fungal aminodeoxychorismate lyase.

Authors:  Javier Botet; Laura Mateos; José L Revuelta; María A Santos
Journal:  Eukaryot Cell       Date:  2007-09-14

10.  Purification and gene cloning of alpha-methylserine aldolase from Ralstonia sp. strain AJ110405 and application of the enzyme in the synthesis of alpha-methyl-L-serine.

Authors:  Hiroyuki Nozaki; Shinji Kuroda; Kunihiko Watanabe; Kenzo Yokozeki
Journal:  Appl Environ Microbiol       Date:  2008-10-24       Impact factor: 4.792

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