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6WK3

Engineered carbene transferase RmaNOD Q52V, putative nitric oxide dioxygenase from Rhodothermus marinus

Summary for 6WK3
Entry DOI10.2210/pdb6wk3/pdb
DescriptorNitric oxide dioxygenase, PROTOPORPHYRIN IX CONTAINING FE, ACETATE ION, ... (5 entities in total)
Functional Keywordsheme binding protein, carbene transferase, globin, metal binding protein
Biological sourceRhodothermus marinus DSM 4252
Total number of polymer chains4
Total formula weight68710.16
Authors
Knight, A.M.,Arnold, F.H. (deposition date: 2020-04-15, release date: 2020-07-08, Last modification date: 2024-03-06)
Primary citationWittmann, B.J.,Knight, A.M.,Hofstra, J.L.,Reisman, S.E.,Kan, S.B.J.,Arnold, F.H.
Diversity-Oriented Enzymatic Synthesis of Cyclopropane Building Blocks.
Acs Catalysis, 10:7112-7116, 2020
Cited by
PubMed Abstract: While biocatalysis is increasingly incorporated into drug development pipelines, it is less commonly used in the early stages of drug discovery. By engineering a protein to produce a chiral motif with a derivatizable functional handle, biocatalysts can be used to help generate diverse building blocks for drug discovery. Here we show the engineering of two variants of nitric oxide dioxygenase (NOD) to catalyze the formation of - and diastereomers of a pinacolboronate-substituted cyclopropane which can be readily derivatized to generate diverse stereopure cyclopropane building blocks.
PubMed: 33282460
DOI: 10.1021/acscatal.0c01888
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.45 Å)
Structure validation

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건을2024-11-13부터공개중

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