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Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|August 8, 2012
Binding of the unreactive substrate analog L-2-amino-3-guanidinopropionic acid (dinor-L-arginine) to human arginase IEdward L D'Antonio, David W ChristiansonJournal of Structural Biology|October 4, 2021
Visualizing transiently associated catalytic domains in assembly-line biosynthesis using cryo-electron microscopyJacque L Faylo, David W ChristiansonMethods in Enzymology|October 14, 2019
Methods for the expression, purification, and crystallization of histone deacetylase 6-inhibitor complexesJeremy D Osko, David W ChristiansonMethods in Enzymology|October 14, 2019
Preparation of a new construct of human histone deacetylase 8 for the crystallization of enzyme-inhibitor complexesNicholas J Porter, David W ChristiansonMethods in Enzymology|June 28, 2024
Methods for the preparation and analysis of the diterpene cyclase fusicoccadiene synthaseEliott S Wenger, David W ChristiansonMethods in Enzymology|June 28, 2024
Methods for the preparation and analysis of a bifunctional class II diterpene synthase, copalyl diphosphate synthase from Penicillium fellutanumMatthew N Gaynes, David W ChristiansonBioorganic & Medicinal Chemistry Letters|February 19, 2020
Structural determinants of affinity and selectivity in the binding of inhibitors to histone deacetylase 6Jeremy D Osko, David W ChristiansonBiochemistry|July 14, 2023
Reprogramming the Cyclization Cascade of epi-Isozizaene Synthase to Generate Alternative Terpene ProductsSamuel A Eaton, David W ChristiansonBiochemistry|March 14, 2018
Polyamine Deacetylase Structure and Catalysis: Prokaryotic Acetylpolyamine Amidohydrolase and Eukaryotic HDAC10Stephen A Shinsky, David W ChristiansonActa Crystallographica. Section F, Structural Biology Communications|September 4, 2020
Binding of inhibitors to active-site mutants of CD1, the enigmatic catalytic domain of histone deacetylase 6Jeremy D Osko, David W ChristiansonPageof 20