Literature summary for 1.5.3.1 extracted from

Shoji, M.; Abe, Y.; Boero, M.; Shigeta, Y.; Nishiya, Y.
Reaction mechanism of N-cyclopropylglycine oxidation by monomeric sarcosine oxidase (2020), Phys. Chem. Chem. Phys., 22, 16552-16561 .

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Inhibitors

Inhibitors	Comment	Organism	Structure
N-cyclopropylglycine	reaction leads to an inactivated species. The polar mechanism is energetically the most favorable. The first rate-limiting step is the N-cyclopropylglycine binding to the flavin ring which simultaneously proceeds with the ring-opening of the N-cyclopropylglycine cyclopropyl group. This step corresponds to the nucleophilic attack of the cyclopropyl group (C3 atom) to the flavin ring (C4a atom)	Bacillus sp. B-0618

Organism

Organism	UniProt	Comment	Textmining
Bacillus sp. B-0618	P40859	-	-

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Release 2023.1 (January 2023)