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Structural basis for the efficient phosphorylation of AZT-MP (3'-azido-3'-deoxythymidine monophosphate) and dGMP by Plasmodium falciparum type I thymidylate kinase

Biochemical journal, 2010-06, Vol.428 (3), p.499-509

2010

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The Rhodococcus equi virulence protein VapA disrupts endolysosome function and stimulates lysosome biogenesis

MicrobiologyOpen (Weinheim), 2017-04, Vol.6 (2), p.np-n/a

2017

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Binding to DNA Protects Neisseria meningitidis Fumarate and Nitrate Reductase Regulator (FNR) from Oxygen

The Journal of biological chemistry, 2010-01, Vol.285 (2), p.1105-1112

2010

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Neisseria meningitidis and Neisseria gonorrhoeae are differently adapted in the regulation of denitrification: single nucleotide polymorphisms that enable species-specific tuning of the aerobic-anaerobic switch

Biochemical journal, 2012-07, Vol.445 (1), p.69-79

2012

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dUTPase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors

Structure (London), 2005-02, Vol.13 (2), p.329-338

2005

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Defining the remarkable structural malleability of a bacterial surface protein Rib domain implicated in infection

Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (52), p.26540-26548

2019

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Structural characterisation of the virulence-associated protein VapG from the horse pathogen Rhodococcus equi

Veterinary microbiology, 2015-08, Vol.179 (1-2), p.42-52

2015

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Synthesis and Evaluation of α‑Thymidine Analogues as Novel Antimalarials

Journal of medicinal chemistry, 2012-12, Vol.55 (24), p.10948-10957

2012

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Insulin at pH 2: Structural Analysis of the Conditions Promoting Insulin Fibre Formation

Journal of molecular biology, 2002-04, Vol.318 (2), p.479-490

2002

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Crystal structures of the GH18 domain of the bifunctional peroxiredoxin–chitinase CotE from Clostridium difficile

Acta crystallographica. Section F, Structural biology communications, 2020-06, Vol.76 (6), p.241-249

2020

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Structure of the virulence-associated protein VapD from the intracellular pathogen Rhodococcus equi

Acta crystallographica. Section D, Biological crystallography., 2014-08, Vol.70 (8), p.2139-2151

2014

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β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase

Bioorganic & medicinal chemistry, 2011-04, Vol.19 (7), p.2378-2391

2011

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Design, Synthesis, and Evaluation of 5′-Diphenyl Nucleoside Analogues as Inhibitors of the Plasmodium falciparum dUTPase

ChemMedChem, 2011-10, Vol.6 (10), p.1816-1831

2011

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Structural Characterization of a β-Diketone Hydrolase from the Cyanobacterium Anabaena sp. PCC 7120 in Native and Product-Bound Forms, a Coenzyme A-Independent Member of the Crotonase Suprafamily

Biochemistry (Easton), 2007-01, Vol.46 (1), p.137-144

2007

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Interactions of Phenol and m-Cresol in the Insulin Hexamer, and Their Effect on the Association Properties of B28 Pro → Asp Insulin Analogues

Biochemistry (Easton), 1998-08, Vol.37 (33), p.11516-11523

1998

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Crystallographic and Solution Studies of N-Lithocholyl Insulin: A New Generation of Prolonged-Acting Human Insulins

Biochemistry (Easton), 2004-05, Vol.43 (20), p.5987-5995

2004

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Crystal Structure of a Prolonged-Acting Insulin with Albumin-Binding Properties

Biochemistry (Easton), 1997-03, Vol.36 (10), p.2826-2831

1997

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Sulfatide promotes the folding of proinsulin, preserves insulin crystals, and mediates its monomerization

Glycobiology (Oxford), 2001-06, Vol.11 (6), p.473-479

2001

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I222 crystal form of despentapeptide (B26-B30) insulin provides new insights into the properties of monomeric insulin

Acta crystallographica. Section D, Biological crystallography., 2006-05, Vol.62 (5), p.505-511

2006

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The 2-A crystal structure of 6-oxo camphor hydrolase. New structural diversity in the crotonase superfamily

The Journal of biological chemistry, 2003-01, Vol.278 (3), p.1744-1750

2003

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Toward the Insulin−IGF-I Intermediate Structures: Functional and Structural Properties of the [TyrB25NMePheB26] Insulin Mutant

Biochemistry (Easton), 2004-12, Vol.43 (51), p.16293-16300

2004

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X-ray Crystallographic Studies on Hexameric Insulins in the Presence of Helix-Stabilizing Agents, Thiocyanate, Methylparaben and Phenol

Biochemistry (Easton), 1995-11, Vol.34 (47), p.15553-15563

1995

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Crystallization and preliminary crystallographic investigation of a low-pH native insulin monomer with flexible behaviour

Acta crystallographica. Section D, Biological crystallography., 2002-01, Vol.58 (1), p.186-187

2002

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The 2-Å Crystal Structure of 6-Oxo Camphor Hydrolase

The Journal of biological chemistry, 2003-01, Vol.278 (3), p.1744-1750

2003

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Structural Consequences of the B5 Histidine → Tyrosine Mutation in Human Insulin Characterized by X-ray Crystallography and Conformational Analysis

Biochemistry (Easton), 1999-09, Vol.38 (37), p.12041-12051

1999

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Structural basis for the efficient phosphorylation of AZT-MP (3'-azido-3'-deoxythymidine monophosphate) and dGMP by Plasmodium falciparum type I thymidylate kinase

The Rhodococcus equi virulence protein VapA disrupts endolysosome function and stimulates lysosome biogenesis

Binding to DNA Protects Neisseria meningitidis Fumarate and Nitrate Reductase Regulator (FNR) from Oxygen

Neisseria meningitidis and Neisseria gonorrhoeae are differently adapted in the regulation of denitrification: single nucleotide polymorphisms that enable species-specific tuning of the aerobic-anaerobic switch

dUTPase as a Platform for Antimalarial Drug Design: Structural Basis for the Selectivity of a Class of Nucleoside Inhibitors

Defining the remarkable structural malleability of a bacterial surface protein Rib domain implicated in infection

Structural characterisation of the virulence-associated protein VapG from the horse pathogen Rhodococcus equi

Synthesis and Evaluation of α‑Thymidine Analogues as Novel Antimalarials

Insulin at pH 2: Structural Analysis of the Conditions Promoting Insulin Fibre Formation

Crystal structures of the GH18 domain of the bifunctional peroxiredoxin–chitinase CotE from Clostridium difficile

Structure of the virulence-associated protein VapD from the intracellular pathogen Rhodococcus equi

β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase

Design, Synthesis, and Evaluation of 5′-Diphenyl Nucleoside Analogues as Inhibitors of the Plasmodium falciparum dUTPase

Structural Characterization of a β-Diketone Hydrolase from the Cyanobacterium Anabaena sp. PCC 7120 in Native and Product-Bound Forms, a Coenzyme A-Independent Member of the Crotonase Suprafamily

Interactions of Phenol and m-Cresol in the Insulin Hexamer, and Their Effect on the Association Properties of B28 Pro → Asp Insulin Analogues

Crystallographic and Solution Studies of N-Lithocholyl Insulin: A New Generation of Prolonged-Acting Human Insulins

Crystal Structure of a Prolonged-Acting Insulin with Albumin-Binding Properties

Sulfatide promotes the folding of proinsulin, preserves insulin crystals, and mediates its monomerization

I222 crystal form of despentapeptide (B26-B30) insulin provides new insights into the properties of monomeric insulin

The 2-A crystal structure of 6-oxo camphor hydrolase. New structural diversity in the crotonase superfamily

Toward the Insulin−IGF-I Intermediate Structures: Functional and Structural Properties of the [TyrB25NMePheB26] Insulin Mutant

X-ray Crystallographic Studies on Hexameric Insulins in the Presence of Helix-Stabilizing Agents, Thiocyanate, Methylparaben and Phenol

Crystallization and preliminary crystallographic investigation of a low-pH native insulin monomer with flexible behaviour

The 2-Å Crystal Structure of 6-Oxo Camphor Hydrolase

Structural Consequences of the B5 Histidine → Tyrosine Mutation in Human Insulin Characterized by X-ray Crystallography and Conformational Analysis

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