A. Boraston

发表

Carbohydrate-binding modules: fine-tuning polysaccharide recognition.

D. Bolam, H. Gilbert, G. Davies, 2004, The Biochemical journal.

Toward Efficient Enzymes for the Generation of Universal Blood through Structure-Guided Directed Evolution.

S. Withers, E. Samain, A. Boraston, 2015, Journal of the American Chemical Society.

Analysis of binding of the family 2a carbohydrate-binding module from Cellulomonas fimi xylanase 10A to cellulose: specificity and identification of functionally important amino acid residues.

C. Haynes, D. Kilburn, N. Gilkes, 2000, Protein engineering.

Glycosylation by Pichia pastoris decreases the affinity of a family 2a carbohydrate-binding module from Cellulomonas fimi: a functional and mutational analysis.

D. Kilburn, A. Boraston, R. Warren, 2001, The Biochemical journal.

O-Glycosylation of a Recombinant Carbohydrate-Binding Module Mutant Secreted by Pichia pastoris

D. Kilburn, A. Boraston, R. Warren, 2003, Journal of Molecular Microbiology and Biotechnology.

Glycoside hydrolase carbohydrate-binding modules as molecular probes for the analysis of plant cell wall polymers.

D. Bolam, H. Gilbert, A. Boraston, 2004, Analytical biochemistry.

Understanding the Biological Rationale for the Diversity of Cellulose-directed Carbohydrate-binding Modules in Prokaryotic Enzymes*

D. Bolam, H. Gilbert, A. Boraston, 2006, Journal of Biological Chemistry.

N-Glycosidase-carbohydrate-binding module fusion proteins as immobilized enzymes for protein deglycosylation.

D. Kilburn, E. Kwan, A. Boraston, 2005, Protein engineering, design & selection : PEDS.

Family 6 Carbohydrate Binding Modules Recognize the Non-reducing End of β-1,3-Linked Glucans by Presenting a Unique Ligand Binding Surface*

H. Gilbert, A. Boraston, C. Morland, 2005, Journal of Biological Chemistry.

Structural and thermodynamic dissection of specific mannan recognition by a carbohydrate binding module, TmCBM27.

Didier Nurizzo, D. Nurizzo, G. Davies, 2003, Structure.

Identification and glucan-binding properties of a new carbohydrate-binding module family.

D. Kilburn, A. Boraston, R. Warren, 2002, The Biochemical journal.

Co‐operative binding of triplicate carbohydrate‐binding modules from a thermophilic xylanase

D. Kilburn, A. Boraston, R. Warren, 2002, Molecular microbiology.

Identification and glucan-binding properties of a new carbohydrate-binding module family.

D. Kilburn, A. Boraston, R. Warren, 2002 .

Carbohydrate-binding Modules Recognize Fine Substructures of Cellulose*

C. Haynes, D. Kilburn, D. Brouwer, 2002, The Journal of Biological Chemistry.

Self‐activating factor X derivative fused to the C‐terminus of a cellulose‐binding module: Production and properties

C. Haynes, D. Kilburn, N. Gilkes, 2002, Biotechnology and bioengineering.

Binding specificity and thermodynamics of a family 9 carbohydrate-binding module from Thermotoga maritima xylanase 10A.

C. Haynes, D. Kilburn, A. Creagh, 2001, Biochemistry.

Differential Oligosaccharide Recognition by Evolutionarily-related β-1,4 and β-1,3 Glucan-binding Modules

Didier Nurizzo, David R. Rose, D. Nurizzo, 2002 .

Characterization and affinity applications of cellulose-binding domains.

C. Haynes, D. Kilburn, N. Gilkes, 1998, Journal of chromatography. B, Biomedical sciences and applications.

A family 2a carbohydrate-binding module suitable as an affinity tag for proteins produced in Pichia pastoris.

D. Kilburn, A. Boraston, B. McLean, 2001, Protein expression and purification.

On-line monitoring and control of methanol concentration in shake-flask cultures of Pichia pastoris.

R T MacGillivray, E Jervis, R. Turner, 1997, Biotechnology and bioengineering.

Glycosylation by Pichia pastoris decreases the affinity of a family 2a carbohydrate-binding module from Cellulomonas fimi: a functional and mutational analysis.

D. Kilburn, A. Boraston, R. Warren, 2001 .

Structural and mechanistic insight into the basis of mucopolysaccharidosis IIIB

A. Boraston, D. Vocadlo, K. Stubbs, 2008, Proceedings of the National Academy of Sciences.

Protein-glycolipid interactions studied in vitro using ESI-MS and nanodiscs: insights into the mechanisms and energetics of binding.

A. Boraston, J. Klassen, John S. Klassen, 2015, Analytical chemistry.

Differential recognition of plant cell walls by microbial xylan-specific carbohydrate-binding modules.

D. Bolam, H. Gilbert, A. Boraston, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Streptococcus pneumoniae endohexosaminidase D; feasibility of using N-glycan oxazoline donors for synthetic glycosylation of a GlcNAc-asparagine acceptor.

A. Boraston, D. Vocadlo, A. Fairbanks, 2010, Organic & biomolecular chemistry.

KdgF, the missing link in the microbial metabolism of uronate sugars from pectin and alginate

A. Boraston, K. Abe, J. Hehemann, 2016, Proceedings of the National Academy of Sciences.

Functional Analyses of Resurrected and Contemporary Enzymes Illuminate an Evolutionary Path for the Emergence of Exolysis in Polysaccharide Lyase Family 2*

A. Boraston, D. W. Abbott, Richard McLean, 2015, The Journal of Biological Chemistry.

Unravelling the Multiple Functions of the Architecturally Intricate Streptococcus pneumoniae β-galactosidase, BgaA

A. B. Dalia, A. Boraston, J. Weiser, 2014, PLoS pathogens.

Metabolism of a hybrid algal galactan by members of the human gut microbiome

Nitin, Xiaohui Xing, A. Boraston, 2022, Nature Chemical Biology.

Advances in understanding the molecular basis of plant cell wall polysaccharide recognition by carbohydrate-binding modules.

H. Gilbert, A. Boraston, J. Knox, 2013, Current opinion in structural biology.

Ab initio phasing of a nucleoside hydrolase‐related hypothetical protein from Saccharophagus degradans that is associated with carbohydrate metabolism

A. Boraston, J. Hehemann, C. Marsters, 2011, Proteins.

Inhibition of the exo-beta-D-glucosaminidase CsxA by a glucosamine-configured castanospermine and an amino-australine analogue.

A. Boraston, R. Brzezinski, K. Stubbs, 2009, Organic & biomolecular chemistry.

The Structure of RdDddP from Roseobacter denitrificans Reveals That DMSP Lyases in the DddP-Family Are Metalloenzymes

A. Boraston, L. Redecke, J. Hehemann, 2014, PloS one.

Diverse modes of galacto-specific carbohydrate recognition by a family 31 glycoside hydrolase from Clostridium perfringens

C. Arrowsmith, S. Houliston, A. Boraston, 2017, PloS one.

The biochemical properties of the Francisella pathogenicity island (FPI)-encoded proteins IglA, IglB, IglC, PdpB and DotU suggest roles in type VI secretion.

K. Hueffer, A. Boraston, C. Schmerk, 2011, Microbiology.

Ten years of CAZypedia: a living encyclopedia of carbohydrate-active enzymes.

Spencer J. Williams, T. Pons, R. Pickersgill, 2018, Glycobiology.

A sweet new wave: structures and mechanisms of enzymes that digest polysaccharides from marine algae.

M. Czjzek, A. Boraston, J. Hehemann, 2014, Current opinion in structural biology.

The interaction of carbohydrate-binding modules with insoluble non-crystalline cellulose is enthalpically driven.

A. Boraston, 2005, The Biochemical journal.

The Glycoprotease CpaA Secreted by Medically Relevant Acinetobacter Species Targets Multiple O-Linked Host Glycoproteins

Nichollas E. Scott, N. Scott, A. Boraston, 2020, mBio.

Recognition of protein-linked glycans as a determinant of peptidase activity

J. Burke, M. Gilbert, W. Wakarchuk, 2017, Proceedings of the National Academy of Sciences.

Cloning, recombinant production, crystallization and preliminary X-ray diffraction analysis of a family 101 glycoside hydrolase from Streptococcus pneumoniae.

A. Boraston, K. Gregg, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

Insights into the recognition of the human glycome by microbial carbohydrate-binding modules.

A. Boraston, E. Ficko-Blean, 2012, Current opinion in structural biology.

A previously uncharacterized O-glycopeptidase from Akkermansia muciniphila requires the Tn-antigen for cleavage of the peptide bond

J. Burke, W. Wakarchuk, A. Boraston, 2022, The Journal of biological chemistry.

Structure of the Streptococcus pneumoniae Surface Protein and Adhesin PfbA

A. Boraston, M. Suits, 2013, PloS one.

Corrigendum: Human gut Bacteroidetes can utilize yeast mannan through a selfish mechanism

Spencer J. Williams, A. Thompson, H. Gilbert, 2015, Nature.

Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of intracellular growth locus E (IglE) protein from Francisella tularensis subsp. novicida.

A. Boraston, F. Nano, C. Robb, 2010, Acta crystallographica. Section F, Structural biology and crystallization communications.

Interactions between Proteins and (1,3)-β-Glucans and Related Polysaccharides

A. Boraston, D. W. Abbott, 2009 .

A novel mechanism of xylan binding by a lectin-like module from Streptomyces lividans xylanase 10A.

D. Kilburn, A. Boraston, P. Tomme, 2000, The Biochemical journal.

Synthesis of 4-methylumbelliferyl α-d-mannopyranosyl-(1→6)-β-d-mannopyranoside and development of a coupled fluorescent assay for GH125 exo-α-1,6-mannosidases.

A. Boraston, D. Vocadlo, R. Mosi, 2013, Bioorganic & medicinal chemistry.

Cloning, recombinant production, crystallization and preliminary X-ray diffraction studies of a family 84 glycoside hydrolase from Clostridium perfringens.

A. Boraston, E. Ficko-Blean, 2005, Acta crystallographica. Section F, Structural biology and crystallization communications.

Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes

A. Boraston, J. Hehemann, E. Martens, 2012, Proceedings of the National Academy of Sciences.

Molecular Characterization of Clinical Rel Mutations and Consequences for Resistance Expression and Fitness in Staphylococcus aureus

A. Boraston, Joanne K. Hobbs, Ashley T Deventer, 2022, Antimicrobial agents and chemotherapy.

(p)ppGpp and the Stringent Response: An Emerging Threat to Antibiotic Therapy.

A. Boraston, Joanne K. Hobbs, 2019, ACS infectious diseases.

The structural basis for exopolygalacturonase activity in a family 28 glycoside hydrolase.

A. Boraston, D. W. Abbott, 2007, Journal of molecular biology.

Structural Biology of Pectin Degradation by Enterobacteriaceae

A. Boraston, D. W. Abbott, 2008, Microbiology and Molecular Biology Reviews.

High-resolution crystal structures of the lectin-like xylan binding domain from Streptomyces lividans xylanase 10A with bound substrates reveal a novel mode of xylan binding.

Spencer J. Williams, D. Kilburn, A. Boraston, 2002, Biochemistry.

Structural analysis of CPF_2247, a novel α‐amylase from Clostridium perfringens

A. Boraston, E. Ficko-Blean, C. Stuart, 2011, Proteins.

CPF_2247, a novel alpha-amylase from Clostridium perfringens

A. Boraston, E. Ficko-Blean, C. Stuart, 2011 .

Clinical Mutations That Partially Activate the Stringent Response Confer Multidrug Tolerance in Staphylococcus aureus

A. Boraston, Joanne K. Hobbs, A. Hettle, 2019, Antimicrobial Agents and Chemotherapy.

Architecturally complex O-glycopeptidases are customized for mucin recognition and hydrolysis

W. Wakarchuk, A. Boraston, E. Ficko-Blean, 2021, Proceedings of the National Academy of Sciences.

The glycoconjugate-degrading enzymes of Clostridium perfringens: tailored catalysts for breaching the intestinal mucus barrier.

A. Boraston, D. W. Abbott, Steven P. Smith, 2020, Glycobiology.

Restricted access of proteins to mannan polysaccharides in intact plant cell walls.

Harry J. Gilbert, Olivier Leroux, William G. T. Willats, 2010, The Plant journal : for cell and molecular biology.

Evidence that family 35 carbohydrate binding modules display conserved specificity but divergent function

S. Firbank, R. Lewis, H. Gilbert, 2009, Proceedings of the National Academy of Sciences.

Sulfatases: Critical Enzymes for Algal Polysaccharide Processing

A. Boraston, C. Vickers, A. Hettle, 2022, Frontiers in Plant Science.

Insights into the κ/ι-carrageenan metabolism pathway of some marine Pseudoalteromonas species

O. Salama-Alber, J. Hui, A. Boraston, 2019, Communications Biology.

The Molecular Basis of Polysaccharide Sulfatase Activity and a Nomenclature for Catalytic Subsites in this Class of Enzyme.

S. Withers, F. Liu, A. Boraston, 2018, Structure.

Human gut Bacteroidetes can utilize yeast mannan through a selfish mechanism

Eric C. Martens, Harry J. Gilbert, Andrew J. Thompson, 2015, Nature.

Iminosugar glycosidase inhibitors: structural and thermodynamic dissection of the binding of isofagomine and 1-deoxynojirimycin to beta-glucosidases.

David L Zechel, G. Davies, A. Boraston, 2003, Journal of the American Chemical Society.

Structural Analysis of a Family 101 Glycoside Hydrolase in Complex with Carbohydrates Reveals Insights into Its Mechanism*

A. Boraston, D. Vocadlo, M. Suits, 2015, The Journal of Biological Chemistry.

The structural basis of substrate recognition in an exo-beta-D-glucosaminidase involved in chitosan hydrolysis.

A. Boraston, A. Fleury, R. Brzezinski, 2009, Journal of molecular biology.

Structural Analysis of a Family 81 Glycoside Hydrolase Implicates Its Recognition of β-1,3-Glucan Quaternary Structure.

A. Boraston, B. Pluvinage, Alexander Fillo, 2017, Structure.

Inhibition of the family 20 glycoside hydrolase catalytic modules in the Streptococcus pneumoniae exo-β-D-N-acetylglucosaminidase, StrH.

A. Boraston, D. Vocadlo, Mitchell Hattie, 2013, Organic & biomolecular chemistry.

Streptococcus pneumoniae Endohexosaminidase D, Structural and Mechanistic Insight into Substrate-assisted Catalysis in Family 85 Glycoside Hydrolases*

Matthew S Macauley, A. Boraston, D. Vocadlo, 2009, Journal of Biological Chemistry.

X-ray crystal structure of a non-crystalline cellulose-specific carbohydrate-binding module: CBM28.

D. Nurizzo, G. Davies, A. Boraston, 2004, Journal of molecular biology.

Carbohydrate recognition by a large sialidase toxin from Clostridium perfringens.

A. Boraston, M. Healey, E. Ficko-Blean, 2007, Biochemistry.

Differential Recognition and Hydrolysis of Host Carbohydrate Antigens by Streptococcus pneumoniae Family 98 Glycoside Hydrolases*

E. Samain, A. Boraston, D. Vocadlo, 2009, The Journal of Biological Chemistry.

Iminosugar-C-glycosides work as pharmacological chaperones of NAGLU, a glycosidase involved in MPS IIIB rare disease.

S. Demotz, D. Alonzi, T. Butters, 2021, Chemistry.

Ab initio structure determination and functional characterization of CBM36; a new family of calcium-dependent carbohydrate binding modules.

J. Turkenburg, G. Davies, A. Boraston, 2004, Structure.

Structure and ligand binding of carbohydrate-binding module CsCBM6-3 reveals similarities with fucose-specific lectins and "galactose-binding" domains.

D. Kilburn, G. Davies, A. Boraston, 2003, Journal of molecular biology.

3.29 – Carbohydrate–Protein Interactions: Carbohydrate-Binding Modules

A. Boraston, D. W. Abbott, A. L. V. Bueren, 2007 .

Structure of a pectin methylesterase from Yersinia enterocolitica.

A. Boraston, D. W. Abbott, 2012, Acta crystallographica. Section F, Structural biology and crystallization communications.

The Active Site of Oligogalacturonate Lyase Provides Unique Insights into Cytoplasmic Oligogalacturonate β-Elimination*

H. Gilbert, A. Boraston, D. W. Abbott, 2010, The Journal of Biological Chemistry.

A Family 2 Pectate Lyase Displays a Rare Fold and Transition Metal-assisted β-Elimination*

A. Boraston, D. W. Abbott, Alisdair B Boraston, 2007, Journal of Biological Chemistry.

Specific recognition of saturated and 4,5-unsaturated hexuronate sugars by a periplasmic binding protein involved in pectin catabolism.

A. Boraston, D. W. Abbott, 2007, Journal of molecular biology.

Biochemical Reconstruction of a Metabolic Pathway from a Marine Bacterium Reveals Its Mechanism of Pectin Depolymerization

A. Boraston, Joanne K. Hobbs, C. Vickers, 2018, Applied and Environmental Microbiology.

Substrate Recognition and Hydrolysis by a Family 50 exo-β-Agarase, Aga50D, from the Marine Bacterium Saccharophagus degradans*

A. Boraston, J. Hehemann, B. Pluvinage, 2013, The Journal of Biological Chemistry.

Blood group antigen recognition by a solute-binding protein from a serotype 3 strain of Streptococcus pneumoniae.

A. Boraston, D. W. Abbott, M. Boulanger, 2009, Journal of molecular biology.

Recognition and Hydrolysis of Noncrystalline Cellulose*

D. Kilburn, E. Kwan, A. Boraston, 2003, The Journal of Biological Chemistry.

Insight into ligand diversity and novel biological roles for family 32 carbohydrate-binding modules.

A. Boraston, D. W. Abbott, J. Eirín-López, 2007, Molecular biology and evolution.

Molecular Characterization of N-glycan Degradation and Transport in Streptococcus pneumoniae and Its Contribution to Virulence

H. Brumer, H. Yesilkaya, A. Boraston, 2017, PLoS pathogens.

Pseudomonas cellulose-binding domains mediate their effects by increasing enzyme substrate proximity.

P. Simpson, D. Bolam, H. Gilbert, 1998, The Biochemical journal.

Mannanase Man26A from Cellulomonas fimi has a mannan-binding module.

D. Stoll, D. Kilburn, H. Stålbrand, 2000, FEMS microbiology letters.

The structural basis of alpha-glucan recognition by a family 41 carbohydrate-binding module from Thermotoga maritima.

A. Boraston, Alicia Lammerts van Bueren, 2007, Journal of molecular biology.

An update on carbohydrate binding modules

P. Simpson, D. Kilburn, B. Svensson, 2002 .

Analysis of Keystone Enzyme in Agar Hydrolysis Provides Insight into the Degradation (of a Polysaccharide from) Red Seaweeds*

A. Boraston, D. Vocadlo, J. Hehemann, 2012, The Journal of Biological Chemistry.

Two complementary alpha-fucosidases fromStreptococcus pneumoniaepromote complete degradation of host-derived carbohydrate antigens.

A. Boraston, Joanne K. Hobbs, Steven P. Smith, 2019 .

Two complementary α-fucosidases from Streptococcus pneumoniae promote complete degradation of host-derived carbohydrate antigens

A. Boraston, Joanne K. Hobbs, Steven P. Smith, 2019, The Journal of Biological Chemistry.

Discovery and characterization of family 39 glycoside hydrolases from rumen anaerobic fungi with polyspecific activity on rare arabinosyl substrates

A. Tsang, R. Forster, A. Boraston, 2017, The Journal of Biological Chemistry.

An Ancestral Member of the Polysaccharide Lyase Family 2 Displays Endolytic Activity and Magnesium Dependence

A. Boraston, D. W. Abbott, Dallas K Thomas, 2013, Applied Biochemistry and Biotechnology.

Structural evidence for a proline-specific glycopeptide recognition domain in an O-glycopeptidase.

A. Boraston, I. Noach, 2020, Glycobiology.

A Structural and Functional Analysis of α-Glucan Recognition by Family 25 and 26 Carbohydrate-binding Modules Reveals a Conserved Mode of Starch Recognition*

A. Boraston, J. Klassen, M. Healey, 2006, Journal of Biological Chemistry.

Structure of the T6SS lipoprotein TssJ1 from Pseudomonas aeruginosa.

A. Boraston, F. Nano, M. Assmus, 2013, Acta crystallographica. Section F, Structural biology and crystallization communications.

Three-dimensional structure of a putative non-cellulosomal cohesin module from a Clostridium perfringens family 84 glycoside hydrolase.

E. Bayer, A. Boraston, Steven P. Smith, 2008, Journal of molecular biology.

Structural analysis of broiler chicken small intestinal mucin O-glycan modification by Clostridium perfringens.

Xiaohui Xing, A. Boraston, R. Uwiera, 2019, Poultry science.

Structural and functional analysis of four family 84 glycoside hydrolases from the opportunistic pathogen Clostridium perfringens.

A. Boraston, B. Pluvinage, Kristyn Burak, 2019, Glycobiology.

The Details of Glycolipid Glycan Hydrolysis by the Structural Analysis of a Family 123 Glycoside Hydrolase from Clostridium perfringens.

A. Boraston, K. Abe, D. Vocadlo, 2016, Journal of molecular biology.

An unusual mode of galactose recognition by a family 32 carbohydrate-binding module.

C. Arrowsmith, S. Houliston, A. Boraston, 2014, Journal of molecular biology.

N-acetylglucosamine recognition by a family 32 carbohydrate-binding module from Clostridium perfringens NagH.

A. Boraston, E. Ficko-Blean, 2009, Journal of molecular biology.

Structural basis of Clostridium perfringens toxin complex formation

E. Bayer, A. Boraston, Steven P. Smith, 2008, Proceedings of the National Academy of Sciences.

Divergent Modes of Glycan Recognition by a New Family of Carbohydrate-binding Modules*♦

A. Boraston, D. W. Abbott, Katie J Gregg, 2008, Journal of Biological Chemistry.

Family 6 Carbohydrate Binding Modules in β-Agarases Display Exquisite Selectivity for the Non-reducing Termini of Agarose Chains*

D. Bolam, H. Gilbert, M. Czjzek, 2006, Journal of Biological Chemistry.

A Second β-Hexosaminidase Encoded in the Streptococcus pneumoniae Genome Provides an Expanded Biochemical Ability to Degrade Host Glycans*

A. Boraston, Joanne K. Hobbs, M. Higgins, 2015, The Journal of Biological Chemistry.

Inhibition of the pneumococcal virulence factor StrH and molecular insights into N-glycan recognition and hydrolysis.

A. B. Dalia, A. Boraston, J. Weiser, 2011, Structure.

Analysis of a New Family of Widely Distributed Metal-independent α-Mannosidases Provides Unique Insight into the Processing of N-Linked Glycans*

A. Boraston, D. Vocadlo, J. Hehemann, 2011, The Journal of Biological Chemistry.

The gastrointestinal pathogen Campylobacter jejuni metabolizes sugars with potential help from commensal Bacteroides vulgatus

H. Nothaft, C. Szymanski, J. Gerlt, 2020, Communications Biology.

Alpha-glucan recognition by a new family of carbohydrate-binding modules found primarily in bacterial pathogens.

J. Ausió, A. Boraston, A. Lammerts van Bueren, 2004, Biochemistry.

beta-1,3-Glucan binding by a thermostable carbohydrate-binding module from Thermotoga maritima.

D. Kilburn, A. Boraston, R. Warren, 2001, Biochemistry.

The structure of PfGH50B, an agarase from the marine bacterium Pseudoalteromonas fuliginea PS47.

A. Boraston, B. Pluvinage, C. Robb, 2020, Acta crystallographica. Section F, Structural biology communications.

Conformational Analysis of the Streptococcus pneumoniae Hyaluronate Lyase and Characterization of Its Hyaluronan-specific Carbohydrate-binding Module

A. Boraston, W. Chai, T. Feizi, 2014, The Journal of Biological Chemistry.

Crystal structures of the family 9 carbohydrate-binding module from Thermotoga maritima xylanase 10A in native and ligand-bound forms.

D. Kilburn, A. Boraston, D. Rose, 2001, Biochemistry.

Analysis of the structural and functional diversity of plant cell wall specific family 6 carbohydrate binding modules.

B. Henrissat, P. Coutinho, H. Gilbert, 2009, Biochemistry.

Portrait of an Enzyme, a Complete Structural Analysis of a Multimodular β-N-Acetylglucosaminidase from Clostridium perfringens*

M. Czjzek, A. Boraston, J. Hehemann, 2009, Journal of Biological Chemistry.

Molecular basis of an agarose metabolic pathway acquired by a human intestinal symbiont

A. Boraston, R. Uwiera, E. Martens, 2018, Nature Communications.

The conformation and function of a multimodular glycogen-degrading pneumococcal virulence factor.

M. Czjzek, U. H. Stroeher, A. Boraston, 2011, Structure.

Identification and structural basis of binding to host lung glycogen by streptococcal virulence factors

Diana Wang, A. Boraston, R. Burke, 2007, Nature Structural &Molecular Biology.

Quantitative approaches to the analysis of carbohydrate-binding module function.

A. Boraston, D. W. Abbott, 2012, Methods in enzymology.

Identification and characterization of a novel periplasmic polygalacturonic acid binding protein from Yersinia enterolitica.

A. Boraston, D. W. Abbott, Susanne Hrynuik, 2007, Journal of molecular biology.

Structure of a glycoside hydrolase family 50 enzyme from a subfamily that is enriched in human gut microbiome bacteroidetes

A. Boraston, B. Pluvinage, K. Giles, 2017, Proteins.

The overall architecture and receptor binding of pneumococcal carbohydrate-antigen-hydrolyzing enzymes.

A. Boraston, T. Lowary, M. Higgins, 2011, Journal of molecular biology.

The structure of a family 110 glycoside hydrolase provides insight into the hydrolysis of α-1,3-galactosidic linkages in λ-carrageenan and blood group antigens

A. Boraston, D. Vocadlo, D. King, 2020, The Journal of Biological Chemistry.

Insights into the κ/ι-carrageenan metabolism pathway of some marine Pseudoalteromonas species

O. Salama-Alber, J. Hui, A. Boraston, 2019, Communications Biology.

The Interaction of a Carbohydrate-binding Module from a Clostridium perfringens N-Acetyl-β-hexosaminidase with Its Carbohydrate Receptor*

A. Boraston, E. Ficko-Blean, 2006, Journal of Biological Chemistry.

The structure of the conserved type six secretion protein TssL (DotU) from Francisella novicida.

A. Boraston, F. Nano, C. Robb, 2012, Journal of molecular biology.

Affinities of human histo-blood group antigens for norovirus capsid protein complexes.

Xi Jiang, A. Boraston, J. Klassen, 2015, Glycobiology.

Structural insights into a unique cellulase fold and mechanism of cellulose hydrolysis

E. Bayer, H. Gilbert, M. Romão, 2011, Proceedings of the National Academy of Sciences.

Carbohydrate Recognition by an Architecturally Complex α-N-Acetylglucosaminidase from Clostridium perfringens

Matthew B. Tessier, R. Woods, A. Boraston, 2012, PloS one.

Endo-fucoidan hydrolases from glycoside hydrolase family 107 (GH107) display structural and mechanistic similarities to α-l-fucosidases from GH29

S. Withers, J. Burke, O. Salama-Alber, 2018, The Journal of Biological Chemistry.

Binding sub-site dissection of a carbohydrate-binding module reveals the contribution of entropy to oligosaccharide recognition at "non-primary" binding subsites.

A. Boraston, A. Lammerts van Bueren, 2004, Journal of molecular biology.

Structural analysis of a bacterial exo-α-D-N-acetylglucosaminidase in complex with an unusual disaccharide found in class III mucin.

A. Boraston, E. Ficko-Blean, 2012, Glycobiology.

The molecular basis of glycogen breakdown and transport in Streptococcus pneumoniae

A. Boraston, D. W. Abbott, M. Higgins, 2010, Molecular microbiology.

Site-specific characterization of the association of xylooligosaccharides with the CBM13 lectin-like xylan binding domain from Streptomyces lividans xylanase 10A by NMR spectroscopy.

Gregory M Lee, L. McIntosh, A. Boraston, 2002, Biochemistry.

Blood Group Antigen Recognition by a Streptococcus pneumoniae Virulence Factor*

Diana Wang, A. Boraston, R. Burke, 2006, Journal of Biological Chemistry.

Structural and functional analysis of fucose-processing enzymes from Streptococcus pneumoniae.

A. Boraston, M. Higgins, M. Suits, 2014, Journal of molecular biology.

Insights into the κ/ι-carrageenan metabolism pathway of some marine Pseudoalteromonas species

O. Salama-Alber, J. Hui, A. Boraston, 2019, Communications Biology.

Differential oligosaccharide recognition by evolutionarily-related beta-1,4 and beta-1,3 glucan-binding modules.

Didier Nurizzo, D. Nurizzo, D. Kilburn, 2002, Journal of molecular biology.

The Structure of the Toxin and Type Six Secretion System Substrate Tse2 in Complex with Its Immunity Protein.

A. Boraston, F. Nano, M. Robb, 2016, Structure.

Separation and Visualization of Glycans by Fluorophore-Assisted Carbohydrate Electrophoresis.

A. Boraston, Joanne K. Hobbs, M. Robb, 2017, Methods in molecular biology.

Properties of a family 56 carbohydrate-binding module and its role in the recognition and hydrolysis of β-1,3-glucan

A. Boraston, K. Abe, D. Langelaan, 2017, The Journal of Biological Chemistry.

Recognition of cello-oligosaccharides by a family 17 carbohydrate-binding module: an X-ray crystallographic, thermodynamic and mutagenic study.

D. Kilburn, A. Boraston, D. Rose, 2001, Journal of molecular biology.

Recognition of the Helical Structure of β-1,4-Galactan by a New Family of Carbohydrate-binding Modules*

B. Henrissat, P. Coutinho, S. Kaneko, 2010, The Journal of Biological Chemistry.

Glycan‐metabolizing enzymes in microbe–host interactions: the Streptococcus pneumoniae paradigm

A. Boraston, Joanne K. Hobbs, B. Pluvinage, 2018, FEBS letters.

A high-throughput screening platform for enzymes active on mucin-type O-glycoproteins

S. Withers, W. Wakarchuk, A. Boraston, 2023, Nature Chemical Biology.

A Fluorogenic Disaccharide Substrate for α-Mannosidases Enables High-Throughput Screening and Identification of an Inhibitor of the GH92 Virulence Factor from Streptococcus pneumoniae.

A. J. Bennet, A. Boraston, D. Vocadlo, 2023, ACS chemical biology.

Pharmacological Chaperones for GCase That Switch Conformation with pH Enhance Enzyme Levels in Gaucher Animal Models.

S. Withers, A. Boraston, D. Vocadlo, 2022, Angewandte Chemie.

The Structure of the Toxin and Type Six Secretion System Substrate Tse2 in Complex with Its Immunity Protein.

A. Boraston, F. Nano, M. Robb, 2016, Structure.

Conformational analysis of StrH, the surface-attached exo-β-D-N-acetylglucosaminidase from Streptococcus pneumoniae.

A. Boraston, D. W. Abbott, J. Grondin, 2012, Journal of molecular biology.

Inhibition of the family 20 glycoside hydrolase catalytic modules in the Streptococcus pneumoniae exo-β-D-N-acetylglucosaminidase, StrH.

A. Boraston, D. Vocadlo, Mitchell Hattie, 2013, Organic & biomolecular chemistry.

NMR assignment of backbone and side chain resonances for a putative protein–protein interaction module from a family 84 glycoside hydrolase of Clostridium perfringens

A. Boraston, Steven P. Smith, S. Chitayat, 2006, Biomolecular NMR assignments.

Inhibition of the pneumococcal virulence factor StrH and molecular insights into N-glycan recognition and hydrolysis.

A. B. Dalia, A. Boraston, D. Vocadlo, 2011, Structure.

Streptococcus pneumoniae Endohexosaminidase D, Structural and Mechanistic Insight into Substrate-assisted Catalysis in Family 85 Glycoside Hydrolases*

Matthew S Macauley, A. Boraston, D. Vocadlo, 2009, Journal of Biological Chemistry.

Discovery and characterization of family 39 glycoside hydrolases from rumen anaerobic fungi with polyspecific activity on rare arabinosyl substrates

A. Tsang, R. Forster, A. Boraston, 2017, The Journal of Biological Chemistry.

Ten years of CAZypedia: a living encyclopedia of carbohydrate-active enzymes.

Spencer J. Williams, T. Pons, R. Pickersgill, 2018, Glycobiology.