1pyy

Revision as of 01:07, 21 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1pyy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pyy, resolution 2.42Å" /> '''Double mutant PBP2x ...)
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Double mutant PBP2x T338A/M339F from Streptococcus pneumoniae strain R6 at 2.4 A resolution

File:1pyy.jpg


1pyy, resolution 2.42Å

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OverviewOverview

PBP2x is a primary determinant of beta-lactams resistance in Streptococcus, pneumoniae. Altered PBP2x with multiple mutations have a reduced, "affinity" for the antibiotics. An important polymorphism is found in, PBP2x sequences from clinical resistant strains. To understand the, mechanism of resistance, it is necessary to identify and characterize the, relevant substitutions. Many similar PBP2x sequences from resistant, isolates have the previously studied T338A mutation, adjacent to the, active site Ser337. We report here the structural and functional analysis, of the M339F substitution that is found in a subset of these sequences, originating from highly resistant strains. The M339F mutation causes a, 4-10-fold reduction of the reaction rate with beta-lactams, depending on, the molecular context. In addition, release of the inactivated antibiotic, from the active site is up to 3-fold faster as a result from the M339F, mutation. These effects measured in vitro are correlated with the level of, beta-lactam resistance in vivo conferred by several PBP2x variants. Thus, a single amino acid difference between similar PBP2x from clinical, isolates can strongly modulate the degree of beta-lactam resistance. The, crystal structure of the double mutant T338A/M339F solved to a resolution, of 2.4 A shows a distortion of the active site and a reorientation of the, hydroxyl group of the active site Ser337, which can explain the kinetic, effects of the mutations.

About this StructureAbout this Structure

1PYY is a Single protein structure of sequence from Streptococcus pneumoniae with SO4, OSU and MPD as ligands. Full crystallographic information is available from OCA.

ReferenceReference

The structural modifications induced by the M339F substitution in PBP2x from Streptococcus pneumoniae further decreases the susceptibility to beta-lactams of resistant strains., Chesnel L, Pernot L, Lemaire D, Champelovier D, Croize J, Dideberg O, Vernet T, Zapun A, J Biol Chem. 2003 Nov 7;278(45):44448-56. Epub 2003 Aug 15. PMID:12923202

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