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Proceedings of the National Academy of Sciences of the United States of America|November 19, 2003
The isoniazid-NAD adduct is a slow, tight-binding inhibitor of InhA, the Mycobacterium tuberculosis enoyl reductase: adduct affinity and drug resistanceRicha Rawat, Adrian Whitty, Peter J TongeAccounts of Chemical Research|January 12, 2022
Photophysics of the Blue Light Using Flavin DomainAndras Lukacs, Peter J Tonge, Stephen R MeechFEBS Letters|August 14, 2003
Ground state isomerization of a model green fluorescent protein chromophoreXiang He, Alasdair F Bell, Peter J TongeCurrent Topics in Medicinal Chemistry|March 10, 2007
Development of modern InhA inhibitors to combat drug resistant strains of Mycobacterium tuberculosisPeter J Tonge, Caroline Kisker, Richard A SlaydenOrganic Letters|April 27, 2002
Synthesis and spectroscopic studies of model red fluorescent protein chromophoresXiang He, Alasdair F Bell, Peter J TongeStructure (London, England : 1993)|January 17, 2012
Structure of the Yersinia pestis FabV enoyl-ACP reductase and its interaction with two 2-pyridone inhibitorsMaria W Hirschbeck, Jochen Kuper, Hao Lu, et al.Methods in Enzymology|May 11, 2019
Vibrational spectroscopy of flavoproteinsJames N Iuliano, Jarrod B French, Peter J TongeBiochemistry|October 16, 2002
Effect of mutagenesis on the stereochemistry of enoyl-CoA hydrataseYuguo Feng, Hilary A Hofstein, Jacque Zwahlen, et al.Bioorganic & Medicinal Chemistry Letters|September 3, 2008
Mechanism-based inhibitors of MenE, an acyl-CoA synthetase involved in bacterial menaquinone biosynthesisXuequan Lu, Huaning Zhang, Peter J Tonge, et al.Journal of the American Chemical Society|June 9, 2005
Ring current effects in the active site of medium-chain Acyl-CoA dehydrogenase revealed by NMR spectroscopyJiaquan Wu, Alasdair F Bell, Andrew A Jaye, et al.Pageof 162