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Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Nature chemical biology, 2018-11, Vol.14 (11), p.995

2018

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Reduction of cysteine sulfinic acid in eukaryotic, typical 2-Cys peroxiredoxins by sulfiredoxin

Antioxidants & redox signaling, 2011-07, Vol.15 (1), p.99

2011

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Novel hyperoxidation resistance motifs in 2-Cys peroxiredoxins

The Journal of biological chemistry, 2018-07, Vol.293 (30), p.11901-11912

2018

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Substrate specificity and membrane topologies of the iron-containing ω3 and ω6 desaturases from Mortierella alpina

Applied microbiology and biotechnology, 2018, Vol.102 (1), p.211-223

2018

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Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria

Journal of the American Society of Nephrology, 2018-06, Vol.29 (6), p.1615-1623

2018

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Cannabinoid Receptor Interacting Protein 1a (CRIP1a): Function and Structure

Molecules (Basel, Switzerland), 2019-10, Vol.24 (20), p.3672

2019

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Molecular Basis for the Resistance of Human Mitochondrial 2-Cys Peroxiredoxin 3 to Hyperoxidation

The Journal of biological chemistry, 2013-10, Vol.288 (41), p.29714-29723

2013

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Kinetic analysis of structural influences on the susceptibility of peroxiredoxins 2 and 3 to hyperoxidation

Biochemical journal, 2016-02, Vol.473 (4), p.411-421

2016

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Metalloaminopeptidases: Common Functional Themes in Disparate Structural Surroundings

Chemical reviews, 2002-12, Vol.102 (12), p.4581-4608

2002

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Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3

Biochimica et biophysica acta. Molecular basis of disease, 2015-12, Vol.1852 (12), p.2700-2705

2015

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Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria

Biochemical journal, 2015-03, Vol.466 (2), p.273-281

2015

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Crystal structure of the thioesterase domain of human fatty acid synthase inhibited by Orlistat

Nature structural & molecular biology, 2007-08, Vol.14 (8), p.704-709

2007

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Mitochondrial peroxiredoxin 3 is more resilient to hyperoxidation than cytoplasmic peroxiredoxins

Biochemical journal, 2009-06, Vol.421 (1), p.51-58

2009

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Structure of the sulphiredoxin-peroxiredoxin complex reveals an essential repair embrace

Nature, 2008-01, Vol.451 (7174), p.98-101

2008

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Free methionine-(R)-sulfoxide reductase from Escherichia coli reveals a new GAF domain function

Proceedings of the National Academy of Sciences - PNAS, 2007-06, Vol.104 (23), p.9597-9602

2007

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Discovery of Heteroaromatic Sulfones As a New Class of Biologically Compatible Thiol-Selective Reagents

ACS chemical biology, 2017-08, Vol.12 (8), p.2201-2208

2017

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Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria

PloS one, 2011-10, Vol.6 (10), p.e26021-e26021

2011

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Expression and purification of integral membrane fatty acid desaturases

PloS one, 2013-03, Vol.8 (3), p.e58139-e58139

2013

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Disabling Mitochondrial Peroxide Metabolism via Combinatorial Targeting of Peroxiredoxin 3 as an Effective Therapeutic Approach for Malignant Mesothelioma

PloS one, 2015-05, Vol.10 (5), p.e0127310

2015

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Peroxiredoxins in Cancer and Response to Radiation Therapies

Antioxidants, 2019-01, Vol.8 (1), p.11

2019

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Cannabinoid Receptor Interacting Protein 1a (CRIP1a) in Health and Disease

Biomolecules (Basel, Switzerland), 2020-11, Vol.10 (12), p.1609

2020

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Metabolism of [13C5]hydroxyproline in vitro and in vivo: implications for primary hyperoxaluria

American journal of physiology: Gastrointestinal and liver physiology, 2012-03, Vol.302 (6), p.G637-G643

2012

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Reduction of Cysteine Sulfinic Acid in Peroxiredoxin by Sulfiredoxin Proceeds Directly through a Sulfinic Phosphoryl Ester Intermediate

The Journal of biological chemistry, 2008-08, Vol.283 (35), p.23846-23851

2008

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Active Site and Loop 4 Movements within Human Glycolate Oxidase: Implications for Substrate Specificity and Drug Design

Biochemistry (Easton), 2008-02, Vol.47 (8), p.2439-2449

2008

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Unique Cellular and Biochemical Features of Human Mitochondrial Peroxiredoxin 3 Establish the Molecular Basis for Its Specific Reaction with Thiostrepton

Antioxidants, 2021-01, Vol.10 (2), p.150

2021

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Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Reduction of cysteine sulfinic acid in eukaryotic, typical 2-Cys peroxiredoxins by sulfiredoxin

Novel hyperoxidation resistance motifs in 2-Cys peroxiredoxins

Substrate specificity and membrane topologies of the iron-containing ω3 and ω6 desaturases from Mortierella alpina

Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria

Cannabinoid Receptor Interacting Protein 1a (CRIP1a): Function and Structure

Molecular Basis for the Resistance of Human Mitochondrial 2-Cys Peroxiredoxin 3 to Hyperoxidation

Kinetic analysis of structural influences on the susceptibility of peroxiredoxins 2 and 3 to hyperoxidation

Metalloaminopeptidases: Common Functional Themes in Disparate Structural Surroundings

Hydroxyproline metabolism in a mouse model of Primary Hyperoxaluria Type 3

Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria

Crystal structure of the thioesterase domain of human fatty acid synthase inhibited by Orlistat

Mitochondrial peroxiredoxin 3 is more resilient to hyperoxidation than cytoplasmic peroxiredoxins

Structure of the sulphiredoxin-peroxiredoxin complex reveals an essential repair embrace

Free methionine-(R)-sulfoxide reductase from Escherichia coli reveals a new GAF domain function

Discovery of Heteroaromatic Sulfones As a New Class of Biologically Compatible Thiol-Selective Reagents

Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria

Expression and purification of integral membrane fatty acid desaturases

Disabling Mitochondrial Peroxide Metabolism via Combinatorial Targeting of Peroxiredoxin 3 as an Effective Therapeutic Approach for Malignant Mesothelioma

Peroxiredoxins in Cancer and Response to Radiation Therapies

Cannabinoid Receptor Interacting Protein 1a (CRIP1a) in Health and Disease

Metabolism of [13C5]hydroxyproline in vitro and in vivo: implications for primary hyperoxaluria

Reduction of Cysteine Sulfinic Acid in Peroxiredoxin by Sulfiredoxin Proceeds Directly through a Sulfinic Phosphoryl Ester Intermediate

Active Site and Loop 4 Movements within Human Glycolate Oxidase: Implications for Substrate Specificity and Drug Design

Unique Cellular and Biochemical Features of Human Mitochondrial Peroxiredoxin 3 Establish the Molecular Basis for Its Specific Reaction with Thiostrepton

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