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Bragg coherent diffraction imaging and metrics for radiation damage in protein micro‐crystallography

Journal of synchrotron radiation, 2017-01, Vol.24 (1), p.83-94

2017

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Aldose reductase structures: implications for mechanism and inhibition

Cellular and molecular life sciences : CMLS, 2004-04, Vol.61 (7-8), p.750-762

2004

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Radiation damage in a micron-sized protein crystal studied via reciprocal space mapping and Bragg coherent diffractive imaging

Structural dynamics (Melville, N.Y.), 2015-07, Vol.2 (4), p.041704-041704

2015

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Three-dimensional reconstruction of the size and shape of protein microcrystals using Bragg coherent diffractive imaging

Journal of optics (2010), 2016-05, Vol.18 (5), p.54003-54011

2016

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Sorbitol dehydrogenase: structure, function and ligand design

Current medicinal chemistry, 2004-02, Vol.11 (4), p.465

2004

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Solvent effects of protic ionic liquids on protein structures

Acta crystallographica. Section A, Foundations and advances, 2023-08, Vol.79 (a2), p.C105-C105

2023

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Liquid crystal phase formation of monoolein in protic ionic liquids

Acta crystallographica. Section A, Foundations and advances, 2023-08, Vol.79 (a2), p.C1134-C1134

2023

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A route to synchrotron nanocrystallography via fluctuation scattering analysis

Acta crystallographica. Section A, Foundations and advances, 2023-08, Vol.79 (a2), p.C553-C553

2023

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A new approach for structure analysis of two‐dimensional membrane protein crystals using X‐ray powder diffraction data

Protein science, 2011-02, Vol.20 (2), p.457-464

2011

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Three-dimensional reconstruction of the size and shape of protein microcrystals using Bragg coherent diffractive imaging

Journal of optics (2010), 2016-03, Vol.18 (5)

2016

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Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with fidarestat and minalrestat: Implications for the binding of cyclic imide inhibitors

Proteins, structure, function, and bioinformatics, 2004-06, Vol.55 (4), p.805-813

2004

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Modelling studies of the active site of human sorbitol dehydrogenase: an approach to structure-based inhibitor design of the enzyme

Bioorganic & medicinal chemistry letters, 2001-12, Vol.11 (24), p.3133-3136

2001

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Structure of the tetrameric form of human L-Xylulose reductase: Probing the inhibitor-binding site with molecular modeling and site-directed mutagenesis

Proteins, structure, function, and bioinformatics, 2005-08, Vol.60 (3), p.424-432

2005

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Radiation damage in a micron-sized protein crystal studied via reciprocal space mapping and Bragg coherent diffractive imaging

Structural dynamics (Melville, N.Y.), 2015-07, Vol.2 (4)

2015

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High-Resolution Structures of Human Aldose Reductase Holoenzyme in Complex with Stereoisomers of the Potent Inhibitor Fidarestat: Stereospecific Interaction between the Enzyme and a Cyclic Imide Type Inhibitor

Journal of medicinal chemistry, 2004-08, Vol.47 (18), p.4530-4537

2004

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Modelling studies on the binding of substrate and inhibitor to the active site of human sorbitol dehydrogenase

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (10), p.1101-1104

2000

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Structure of human aldose reductase holoenzyme in complex with Statil: An approach to structure-based inhibitor design of the enzyme

Proteins, structure, function, and bioinformatics, 2003-02, Vol.50 (2), p.230-238

2003

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Probing the ultra-high resolution structure of aldose reductase with molecular modelling and noncovalent mass spectrometry

Bioorganic & medicinal chemistry, 2004-07, Vol.12 (14), p.3797-3806

2004

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Crystal structure of human L-xylulose reductase holoenzyme: Probing the role of Asn107 with site-directed mutagenesis

Proteins, structure, function, and bioinformatics, 2004-05, Vol.55 (3), p.724-732

2004

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Characterisation of an autoreactive conformational epitope on GAD65 recognised by the human monoclonal antibody b78 using a combination of phage display, in vitro mutagenesis and molecular modelling

Journal of autoimmunity, 2006-05, Vol.26 (3), p.172-181

2006

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Towards protein structure determination using two-dimensional crystals and powders

Acta crystallographica. Section A, Foundations of crystallography, 2008-08, Vol.64 (a1), p.C180-C180

2008

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Structure analysis of two-dimensional membrane proteins using X-ray powder diffraction data

Acta crystallographica. Section A, Foundations of crystallography, 2011-08, Vol.67 (a1), p.C591-C592

2011

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Structure-based design of inhibitors of human l-xylulose reductase modelled into the active site of the enzyme

Bioorganic & medicinal chemistry letters, 2003-04, Vol.13 (8), p.1469-1474

2003

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Expression, purification and preliminary crystallographic analysis of human sorbitol dehydrogenase

Acta crystallographica. Section D, Biological crystallography., 2003-03, Vol.59 (3), p.558-560

2003

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Inhibitor binding to aldose reductase studied at subatomic resolution

Acta crystallographica. Section A, Foundations of crystallography, 2005-08, Vol.61 (a1), p.c122-c122

2005

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Bragg coherent diffraction imaging and metrics for radiation damage in protein micro‐crystallography

Aldose reductase structures: implications for mechanism and inhibition

Radiation damage in a micron-sized protein crystal studied via reciprocal space mapping and Bragg coherent diffractive imaging

Three-dimensional reconstruction of the size and shape of protein microcrystals using Bragg coherent diffractive imaging

Sorbitol dehydrogenase: structure, function and ligand design

Solvent effects of protic ionic liquids on protein structures

Liquid crystal phase formation of monoolein in protic ionic liquids

A route to synchrotron nanocrystallography via fluctuation scattering analysis

A new approach for structure analysis of two‐dimensional membrane protein crystals using X‐ray powder diffraction data

Three-dimensional reconstruction of the size and shape of protein microcrystals using Bragg coherent diffractive imaging

Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with fidarestat and minalrestat: Implications for the binding of cyclic imide inhibitors

Modelling studies of the active site of human sorbitol dehydrogenase: an approach to structure-based inhibitor design of the enzyme

Structure of the tetrameric form of human L-Xylulose reductase: Probing the inhibitor-binding site with molecular modeling and site-directed mutagenesis

Radiation damage in a micron-sized protein crystal studied via reciprocal space mapping and Bragg coherent diffractive imaging

High-Resolution Structures of Human Aldose Reductase Holoenzyme in Complex with Stereoisomers of the Potent Inhibitor Fidarestat: Stereospecific Interaction between the Enzyme and a Cyclic Imide Type Inhibitor

Modelling studies on the binding of substrate and inhibitor to the active site of human sorbitol dehydrogenase

Structure of human aldose reductase holoenzyme in complex with Statil: An approach to structure-based inhibitor design of the enzyme

Probing the ultra-high resolution structure of aldose reductase with molecular modelling and noncovalent mass spectrometry

Crystal structure of human L-xylulose reductase holoenzyme: Probing the role of Asn107 with site-directed mutagenesis

Characterisation of an autoreactive conformational epitope on GAD65 recognised by the human monoclonal antibody b78 using a combination of phage display, in vitro mutagenesis and molecular modelling

Towards protein structure determination using two-dimensional crystals and powders

Structure analysis of two-dimensional membrane proteins using X-ray powder diffraction data

Structure-based design of inhibitors of human l-xylulose reductase modelled into the active site of the enzyme

Expression, purification and preliminary crystallographic analysis of human sorbitol dehydrogenase

Inhibitor binding to aldose reductase studied at subatomic resolution

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