6mvf

From Proteopedia

Crystal structure of FMN-binding beta-glucuronidase from Facaelibacterium prausnitzii L2-6

PDB ID 6mvf

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Structural highlights

6mvf is a 6 chain structure with sequence from Faecalibacterium prausnitzii L2-6. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:	X-ray diffraction, Resolution 2.55Å
Ligands:
Resources:	FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

D4K3H3_9FIRM

Publication Abstract from PubMed

The human gut microbiota encodes beta-glucuronidases (GUS) that play key roles in health and disease via the metabolism of glucuronate-containing carbohydrates and drugs. Hundreds of putative bacterial GUS enzymes have been identified by metagenomic analysis of the human gut microbiome, but less than 10% have characterized structures and functions. Here we describe a set of unique gut microbial GUS enzymes that bind flavin mononucleotide (FMN). First, we show using mass spectrometry, isothermal titration calorimetry, and x-ray crystallography that a purified GUS from the gut commensal microbe Faecalibacterium prausnitzii binds to FMN on a surface groove located 30A away from the active site. Second, utilizing structural and functional data from this FMN-binding GUS, we analyzed the 279 unique GUS sequences from the human microbiome project database and identified 14 putative FMN-binding GUSs. We characterized four of these hits and solved the structure of two, the GUSs from Ruminococcus gnavus and Roseburia hominis, which confirmed that these are FMN binders. Third, binding and kinetic analysis of the FMN-binding site mutants of these five GUSs show that they utilize a conserved site to bind FMN that is not essential for GUS activity, but can affect KM. Lastly, a comprehensive structural review of the PDB reveals that the FMN-binding site employed by these enzymes is unlike any structurally characterized FMN-binders to date. These findings reveal the first instance of an FMN-binding glycoside hydrolase and suggest a potential link between FMN and carbohydrate metabolism in the human gut microbiota.

Discovery and Characterization of FMN-Binding beta-Glucuronidases in the Human Gut Microbiome.,Pellock SJ, Walton WG, Ervin SM, Torres-Rivera D, Creekmore BC, Bergan G, Dunn ZD, Li B, Tripathy A, Redinbo MR J Mol Biol. 2019 Jan 15. pii: S0022-2836(19)30011-7. doi:, 10.1016/j.jmb.2019.01.013. PMID:30658055^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

↑ Pellock SJ, Walton WG, Ervin SM, Torres-Rivera D, Creekmore BC, Bergan G, Dunn ZD, Li B, Tripathy A, Redinbo MR. Discovery and Characterization of FMN-Binding beta-Glucuronidases in the Human Gut Microbiome. J Mol Biol. 2019 Jan 15. pii: S0022-2836(19)30011-7. doi:, 10.1016/j.jmb.2019.01.013. PMID:30658055 doi:http://dx.doi.org/10.1016/j.jmb.2019.01.013