Graham Moran

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Loyola University Chicago

United States

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About

Professor Graham Moran is a faculty member at Loyola University Chicago, specializing in enzymology and catalytic mechanisms. His recent research includes investigations into dihydroorotate dehydrogenases, flavoprotein oxidoreductases, and the catalytic sequences in various biochemical processes. He is actively contributing to the understanding of electron distribution and enzyme activity through advanced kinetic analyses.

Recent Grants

Grant: Close

Collaborative Research: The Chemistry of Riboflavin Biosynthesis

Open Date: 2019-08-01

Close Date: 2022-07-31

Grant: Close

Redefining Renalase

Open Date: 2018-09-01

Close Date: 2019-06-30

Grant: Close

2017 Enzymes, Coenzymes and Metabolic Pathways Gordon Research Conference and Gordon Research Seminar

Open Date: 2017-07-14

Close Date: 2018-06-30

Grant: Close

MRI: Acquisition of a 500 MHz Nuclear Magnetic Resonance (NMR) Spectrometer to Enhance NMR Capabilities at a Major Urban Research Institution

Open Date: 2016-09-01

Close Date: 2019-08-31

Grant: Close

Redefining Renalase

Open Date: 2014-07-01

Close Date: 2019-05-31

Articles (20)

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2021

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2021

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2021

Collaborators (6)

Audrey Lamb

Professor and Chair

University of Texas at San Antonio

UNITED STATES

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Natsuko Kondo

Assistant professor

Institute for Integrated Radiation and Nuclear Science, Kyoto University

JAPAN

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Daniel P. Becker

Loyola University Chicago

UNITED STATES

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Peter Doubleday

ETH Zürich

SWITZERLAND

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Hiroki Ueda

Assistant Professor

Institute of Science Tokyo

JAPAN

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Dali Liu

Professor

Loyola University Chicago

UNITED STATES

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Graham Moran

Research Interests

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About

Recent Grants

Articles (20)

Electron Pushing: Variants That Alter the Catalytic Distribution of Electrons in Dihydroorotate Dehydrogenase 1B from Lactococcus lactis

Dihydropyrimidine Dehydrogenase from Escherichia coli: Evidence for the Catalytic Sequence

The binding modes of quinones in flavoprotein oxidoreductases

Not Once, not Twice, but Thrice: Structure and Catalytic Mechanisms of the Dihydroorotate Dehydrogenases

Using Transient State Kinetics to Contextualize the Catalytic Strategy of Human Ferroptosis Suppressor Protein 1

More Pieces of the Puzzle: Transient State Analysis of Dihydroorotate Dehydrogenase B from Lactoccocus lactis

Probing the site of glutathione reduction by thioredoxin/glutathione reductase from Schistosoma mansoni under anaerobic conditions

Correction to “Design, Synthesis, and Mechanistic Studies of (R)-3-Amino-5,5-difluorocyclohex-1-ene-1-carboxylic Acid as an Inactivator of Human Ornithine Aminotransferase”

Elucidation of the Catalytic Sequence of Dihydroorotate Dehydrogenase B from Lactoccocus lactis: Evidence for Accumulation of a Flavin Bisemiquinone State in Catalysis

Design, Synthesis, and Mechanistic Studies of (R)-3-Amino-5,5-difluorocyclohex-1-ene-1-carboxylic Acid as an Inactivator of Human Ornithine Aminotransferase

Correction to “Rational Design, Synthesis, and Mechanism of (3S,4R)-3-Amino-4-(difluoromethyl)cyclopent-1-ene-1-carboxylic Acid: Employing a Second-Deprotonation Strategy for Selectivity of Human Ornithine Aminotransferase over GABA Aminotransferase”

Descriptive Analysis of Transient-State Observations for Thioredoxin/Glutathione Reductase (Sec597Cys) from Schistosoma mansoni

Carborane-Containing Hydroxamate MMP Ligands for the Treatment of Tumors Using Boron Neutron Capture Therapy (BNCT): Efficacy without Tumor Cell Entry

Mammalian dihydropyrimidine dehydrogenase: Added mechanistic details from transient-state analysis of charge transfer complexes

Evidence for the Chemical Mechanism of RibB (3,4-Dihydroxy-2-butanone 4-phosphate Synthase) of Riboflavin Biosynthesis

Rational Design, Synthesis, and Mechanism of (3S,4R)-3-Amino-4-(difluoromethyl)cyclopent-1-ene-1-carboxylic Acid: Employing a Second-Deprotonation Strategy for Selectivity of Human Ornithine Aminotransferase over GABA Aminotransferase

Finding Ways to Relax: A Revisionistic Analysis of the Chemistry of <i>E. coli</i> GTP Cyclohydrolase II.

Mammalian dihydropyrimidine dehydrogenase

Perturbing the Movement of Hydrogens to Delineate and Assign Events in the Reductive Activation and Turnover of Porcine Dihydropyrimidine Dehydrogenase

Turnover and Inactivation Mechanisms for (S)-3-Amino-4,4-difluorocyclopent-1-enecarboxylic Acid, a Selective Mechanism-Based Inactivator of Human Ornithine Aminotransferase

Collaborators (6)

Audrey Lamb

Natsuko Kondo

Daniel P. Becker

Peter Doubleday

Hiroki Ueda

Dali Liu

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