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Journal Article | FZJ-2021-03549 |
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2021
Soc.
Cambridge
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Please use a persistent id in citations: http://hdl.handle.net/2128/29752 doi:10.1039/D0CC08226K
Abstract: Semi-rational redesign of the substrate binding pocket and access tunnels of prodigiosin ligase PigC enhanced the catalytic efficiency in the synthesis of pyrrolic anti-cancer agents more than 45 times. A molecular understanding was gained on residues V333 and T334 relevant to substrate binding and translocation of small pyrroles through PigC access tunnels.
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