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Bioorganic & Medicinal Chemistry Letters|October 1, 2014
Ejection of structural zinc leads to inhibition of γ-butyrobetaine hydroxylaseAnna M Rydzik, Jürgen Brem, Weston B Struwe, et al.
Chembiochem : a European Journal of Chemical Biology|March 9, 2026
Structural and Functional Validation of Pseudomonas Savastanoi Ethylene Forming Enzymes Reveals Flexibility in 2-Oxoglutarate Binding Mode and ConformationYihong Sun, Siddhant Dhingra, Mark D Allen, et al.
Angewandte Chemie (International Ed. in English)|April 22, 2021
Human Oxygenase Variants Employing a Single Protein FeII Ligand Are Catalytically ActiveAmelia Brasnett, Inga Pfeffer, Lennart Brewitz, et al.
Biochemistry|April 27, 2005
Structural studies on the reaction of isopenicillin N synthase with the truncated substrate analogues delta-(L-alpha-aminoadipoyl)-L-cysteinyl-glycine and delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-alanineAlexandra J Long, Ian J Clifton, Peter L Roach, et al.
The Journal of Biological Chemistry|March 16, 2002
X-ray structure of a serine protease acyl-enzyme complex at 0.95-A resolutionGergely Katona, Rupert C Wilmouth, Penny A Wright, et al.
Progress in Lipid Research|June 20, 2003
The chemical biology of branched-chain lipid metabolismMridul Mukherji, Christopher J Schofield, Anthony S Wierzbicki, et al.
Nature Chemical Biology|August 7, 2007
Structural and mechanistic basis of penicillin-binding protein inhibition by lactivicinsPauline Macheboeuf, Delphine S Fischer, Tom Brown, et al.
Chemical Communications (Cambridge, England)|November 30, 2013
Structural insights into how 5-hydroxymethylation influences transcription factor bindingLukas Lercher, Michael A McDonough, Afaf H El-Sagheer, et al.
Nucleic Acids Research|August 13, 2021
A phosphate binding pocket is a key determinant of exo- versus endo-nucleolytic activity in the SNM1 nuclease familyHannah T Baddock, Joseph A Newman, Yuliana Yosaatmadja, et al.
RSC Medicinal Chemistry|November 7, 2025
C6-Alkoxy substituted penicillins are potent non-covalently binding inhibitors of the SARS-CoV-2 main proteaseDorian-Gabriel Muntean, Wojtek Treyde, Linda Kinena, et al.
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