about
Crystal structures of Pseudomonas putida esterase reveal the functional role of residues 187 and 287 in substrate binding and chiral recognitionSwitching a newly discovered lactonase into an efficient and thermostable phosphotriesterase by simple double mutations His250Ile/Ile263TrpReshaping an enzyme binding pocket for enhanced and inverted stereoselectivity: use of smallest amino acid alphabets in directed evolutionEngineering of an epoxide hydrolase for efficient bioresolution of bulky pharmaco substrates.A smart library of epoxide hydrolase variants and the top hits for synthesis of (S)-β-blocker precursors.Protein engineering of aldolase LbDERA for enhanced activity toward real substrates with a high-throughput screening method coupled with an aldehyde dehydrogenase.Engineering Streptomyces coelicolor Carbonyl Reductase for Efficient Atorvastatin Precursor Synthesis.Structural and Computational Insight into the Catalytic Mechanism of Limonene Epoxide Hydrolase Mutants in Stereoselective Transformations.Bypassing bacterial infection in phage display by sequencing DNA released from phage particles.Phage Selection of Cyclic Peptides for Application in Research and Drug Development.Cyclization of peptides with two chemical bridges affords large scaffold diversitiesThiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligandsDe novo development of proteolytically resistant therapeutic peptides for oral administration
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Xu-Dong Kong
@ast
Xu-Dong Kong
@en
Xu-Dong Kong
@es
Xu-Dong Kong
@nl
type
label
Xu-Dong Kong
@ast
Xu-Dong Kong
@en
Xu-Dong Kong
@es
Xu-Dong Kong
@nl
prefLabel
Xu-Dong Kong
@ast
Xu-Dong Kong
@en
Xu-Dong Kong
@es
Xu-Dong Kong
@nl
P106
P31
P496
0000-0003-3216-7545