5bxa

Structure of PslG from Pseudomonas aeruginosa in complex with mannose

spinqualitylabelsall models 5bxa, resolution 1.90Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5bxa is a 1 chain structure with sequence from Pseudomonas aeruginosa PAO1. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.9Å Ligands: CD, CL, EDO, MAN Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function Q9I1N2_PSEAE Publication Abstract from PubMed A key component of colonization, biofilm formation, and protection of the opportunistic human pathogen Pseudomonas aeruginosa is the biosynthesis of the exopolysaccharide Psl. Composed of a pentameric repeating unit of mannose, glucose and rhamnose, the biosynthesis of Psl is proposed to occur via a Wzx/Wzy-dependent mechanism. Previous genetic studies have shown that the putative glycoside hydrolase PslG is essential for Psl biosynthesis. To understand the function of this protein, the apo structure of the periplasmic domain of PslG (PslG31-442) and its complex with mannose were determined to 2.0 and 1.9 A resolution, respectively. Despite similar domain architecture and positioning of catalytic residues to other family 39 glycoside hydrolases (GH39), PslG31-442 exhibits a unique 32 A long active site groove that is distinct from other structurally characterized family members. PslG formed a complex with two mannose monosaccharides in this groove, consistent with binding data obtained from intrinsic tryptophan fluorescence. PslG was able to catalyze the hydrolysis of surface-associated Psl and this activity was abolished in a E165Q/E276Q double catalytic variant. Surprisingly, P. aeruginosa variants with these chromosomal mutations as well as a pslG deletion mutant were still capable of forming Psl biofilms. However, overexpression of PslG in a pslG deletion background impaired biofilm formation and resulted in less surface-associated Psl, suggesting that regulation of this enzyme is important during polysaccharide biosynthesis. Characterization of the Pseudomonas aeruginosa Glycoside Hydrolase PslG Reveals that its Levels are Critical for Psl Polysaccharide Biosynthesis and Biofilm Formation.,Baker P, Whitfield GB, Hill PJ, Little DJ, Pestrak MJ, Robinson H, Wozniak DJ, Howell PL J Biol Chem. 2015 Sep 30. pii: jbc.M115.674929. PMID:26424791 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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