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5IPY

Crystal structure of WT RnTmm

Summary for 5IPY
Entry DOI10.2210/pdb5ipy/pdb
Related5IQ1 5IQ4
DescriptorFlavin-containing monooxygenase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, FLAVIN-ADENINE DINUCLEOTIDE, ... (4 entities in total)
Functional Keywordsflavin-containing monooxygenase, flavoprotein
Biological sourceRoseovarius nubinhibens (strain ATCC BAA-591 / DSM 15170 / ISM)
Total number of polymer chains2
Total formula weight106583.29
Authors
Li, C.Y.,Zhang, Y.Z. (deposition date: 2016-03-10, release date: 2017-01-18, Last modification date: 2023-11-08)
Primary citationLi, C.Y.,Chen, X.L.,Zhang, D.,Wang, P.,Sheng, Q.,Peng, M.,Xie, B.B.,Qin, Q.L.,Li, P.Y.,Zhang, X.Y.,Su, H.N.,Song, X.Y.,Shi, M.,Zhou, B.C.,Xun, L.Y.,Chen, Y.,Zhang, Y.Z.
Structural mechanism for bacterial oxidation of oceanic trimethylamine into trimethylamine N-oxide
Mol. Microbiol., 103:992-1003, 2017
Cited by
PubMed Abstract: Trimethylamine (TMA) and trimethylamine N-oxide (TMAO) are widespread in the ocean and are important nitrogen source for bacteria. TMA monooxygenase (Tmm), a bacterial flavin-containing monooxygenase (FMO), is found widespread in marine bacteria and is responsible for converting TMA to TMAO. However, the molecular mechanism of TMA oxygenation by Tmm has not been explained. Here, we determined the crystal structures of two reaction intermediates of a marine bacterial Tmm (RnTmm) and elucidated the catalytic mechanism of TMA oxidation by RnTmm. The catalytic process of Tmm consists of a reductive half-reaction and an oxidative half-reaction. In the reductive half-reaction, FAD is reduced and a C4a-hydroperoxyflavin intermediate forms. In the oxidative half-reaction, this intermediate attracts TMA through electronic interactions. After TMA binding, NADP bends and interacts with D317, shutting off the entrance to create a protected micro-environment for catalysis and exposing C4a-hydroperoxyflavin to TMA for oxidation. Sequence analysis suggests that the proposed catalytic mechanism is common for bacterial Tmms. These findings reveal the catalytic process of TMA oxidation by marine bacterial Tmm and first show that NADP undergoes a conformational change in the oxidative half-reaction of FMOs.
PubMed: 27997715
DOI: 10.1111/mmi.13605
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.5 Å)
Structure validation

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数据于2025-06-25公开中

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