1pyy: Difference between revisions

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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caption="1pyy, resolution 2.42&Aring;" />
'''Double mutant PBP2x T338A/M339F from Streptococcus pneumoniae strain R6 at 2.4 A resolution'''<br />
'''Double mutant PBP2x T338A/M339F from Streptococcus pneumoniae strain R6 at 2.4 A resolution'''<br />


==Overview==
==Overview==
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.
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 Structure==
==About this Structure==
1PYY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptococcus_pneumoniae Streptococcus pneumoniae] with SO4, OSU and MPD as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PYY OCA].  
1PYY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptococcus_pneumoniae Streptococcus pneumoniae] with <scene name='pdbligand=SO4:'>SO4</scene>, <scene name='pdbligand=OSU:'>OSU</scene> and <scene name='pdbligand=MPD:'>MPD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PYY OCA].  


==Reference==
==Reference==
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[[Category: transmembrane]]
[[Category: transmembrane]]


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