Patrick Rabe

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University of Oxford

United Kingdom

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Systematische Mutagenese und Kristallisationsexperimente der Isopenicillin N-Synthase zur Herstellung von neuen klinisch relevanten beta-Lactam-Antibiotika und beta–Lactamse-Inhibitoren

Open Date: 2017-04-01

Close Date: 2019-03-01

Grant: Close

Structural insights into O2 activation and dynamics during Luciferase catalysis with a new fixed target device enabling rapid O2 reaction initiation

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Articles (10)

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2025

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2025

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

Collaborators (6)

Jurgen Brem

University of Oxford

UNITED KINGDOM

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Chiara Bardella

UNITED KINGDOM

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Chris Schofield

University of Oxford

UNITED KINGDOM

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Christopher T. Lohans

Queen's University

CANADA

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Christopher Schofield

University of Oxford

UNITED KINGDOM

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Lennart Brewitz

University of Oxford

UNITED KINGDOM

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Patrick Rabe

Research Interests

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Contact this professor

Recent Grants

Articles (10)

Targeting mycobacterial transpeptidases: evaluating the roles of Ldt and PBP inhibition in suppressing Mycobacterium smegmatis

Filamin C dimerisation is regulated by HSPB7

Biochemical and crystallographic studies of l,d-transpeptidase 2 from Mycobacterium tuberculosis with its natural monomer substrate

JmjC catalysed histone H2a N-methyl arginine demethylation and C4-arginine hydroxylation reveals importance of sequence-reactivity relationships

Natural and synthetic 2-oxoglutarate derivatives are substrates for oncogenic variants of human isocitrate dehydrogenase 1 and 2

Interactions of hydrolyzed β-lactams with the L1 metallo-β-lactamase: Crystallography supports stereoselective binding of cephem/carbapenem products

Resistance to the isocitrate dehydrogenase 1 mutant inhibitor ivosidenib can be overcome by alternative dimer-interface binding inhibitors.

Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane

Spectroscopic studies reveal details of substrate-induced conformational changes distant from the active site in isopenicillin N synthase

Studies on enmetazobactam clarify mechanisms of widely used β-lactamase inhibitors

Collaborators (6)

Jurgen Brem

Chiara Bardella

Chris Schofield

Christopher T. Lohans

Christopher Schofield

Lennart Brewitz

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