Literature DB >> 11846551

Homology between O-linked GlcNAc transferases and proteins of the glycogen phosphorylase superfamily.

J O Wrabl1, N V Grishin.   

Abstract

The O-linked GlcNAc transferases (OGTs) are a recently characterized group of largely eukaryotic enzymes that add a single beta-N-acetylglucosamine moiety to specific serine or threonine hydroxyls. In humans, this process may be part of a sugar regulation mechanism or cellular signaling pathway that is involved in many important diseases, such as diabetes, cancer, and neurodegeneration. However, no structural information about the human OGT exists, except for the identification of tetratricopeptide repeats (TPR) at the N terminus. The locations of substrate binding sites are unknown and the structural basis for this enzyme's function is not clear. Here, remote homology is reported between the OGTs and a large group of diverse sugar processing enzymes, including proteins with known structure such as glycogen phosphorylase, UDP-GlcNAc 2-epimerase, and the glycosyl transferase MurG. This relationship, in conjunction with amino acid similarity spanning the entire length of the sequence, implies that the fold of the human OGT consists of two Rossmann-like domains C-terminal to the TPR region. A conserved motif in the second Rossmann domain points to the UDP-GlcNAc donor binding site. This conclusion is supported by a combination of statistically significant PSI-BLAST hits, consensus secondary structure predictions, and a fold recognition hit to MurG. Additionally, iterative PSI-BLAST database searches reveal that proteins homologous to the OGTs form a large and diverse superfamily that is termed GPGTF (glycogen phosphorylase/glycosyl transferase). Up to one-third of the 51 functional families in the CAZY database, a glycosyl transferase classification scheme based on catalytic residue and sequence homology considerations, can be unified through this common predicted fold. GPGTF homologs constitute a substantial fraction of known proteins: 0.4% of all non-redundant sequences and about 1% of proteins in the Escherichia coli genome are found to belong to the GPGTF superfamily. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11846551     DOI: 10.1006/jmbi.2001.5151

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  34 in total

1.  Three monophyletic superfamilies account for the majority of the known glycosyltransferases.

Authors:  Jing Liu; Arcady Mushegian
Journal:  Protein Sci       Date:  2003-07       Impact factor: 6.725

Review 2.  The roles of O-linked β-N-acetylglucosamine in cardiovascular physiology and disease.

Authors:  Natasha E Zachara
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-01-27       Impact factor: 4.733

3.  Crystallization and preliminary crystallographic analysis of PimA, an essential mannosyltransferase from Mycobacterium smegmatis.

Authors:  Marcelo E Guerin; Alejandro Buschiazzo; Jana Korduláková; Mary Jackson; Pedro M Alzari
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-04-22

4.  Conformational plasticity of the essential membrane-associated mannosyltransferase PimA from mycobacteria.

Authors:  David Giganti; Jorge Alegre-Cebollada; Saioa Urresti; David Albesa-Jové; Ane Rodrigo-Unzueta; Natalia Comino; Michael Kachala; Sonia López-Fernández; Dmitri I Svergun; Julio M Fernández; Marcelo E Guerin
Journal:  J Biol Chem       Date:  2013-08-20       Impact factor: 5.157

Review 5.  Structure-function relationships of membrane-associated GT-B glycosyltransferases.

Authors:  David Albesa-Jové; David Giganti; Mary Jackson; Pedro M Alzari; Marcelo E Guerin
Journal:  Glycobiology       Date:  2013-11-18       Impact factor: 4.313

6.  The structure of sucrose phosphate synthase from Halothermothrix orenii reveals its mechanism of action and binding mode.

Authors:  Teck Khiang Chua; Janusz M Bujnicki; Tien-Chye Tan; Frederick Huynh; Bharat K Patel; J Sivaraman
Journal:  Plant Cell       Date:  2008-04-18       Impact factor: 11.277

Review 7.  The making of a sweet modification: structure and function of O-GlcNAc transferase.

Authors:  John Janetzko; Suzanne Walker
Journal:  J Biol Chem       Date:  2014-10-21       Impact factor: 5.157

8.  Dynamic O-GlcNAcylation and its roles in the cellular stress response and homeostasis.

Authors:  Jennifer A Groves; Albert Lee; Gokben Yildirir; Natasha E Zachara
Journal:  Cell Stress Chaperones       Date:  2013-04-26       Impact factor: 3.667

9.  Crystal structure of the MurG:UDP-GlcNAc complex reveals common structural principles of a superfamily of glycosyltransferases.

Authors:  Yanan Hu; Lan Chen; Sha Ha; Ben Gross; Brian Falcone; Deborah Walker; Maryam Mokhtarzadeh; Suzanne Walker
Journal:  Proc Natl Acad Sci U S A       Date:  2003-01-21       Impact factor: 11.205

10.  Bacterial β-Kdo glycosyltransferases represent a new glycosyltransferase family (GT99).

Authors:  Olga G Ovchinnikova; Evan Mallette; Akihiko Koizumi; Todd L Lowary; Matthew S Kimber; Chris Whitfield
Journal:  Proc Natl Acad Sci U S A       Date:  2016-05-19       Impact factor: 11.205

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