This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


2jch

From Proteopedia

Revision as of 16:25, 5 November 2007 by OCA (Talk | contribs)
Jump to: navigation, search

2jch, resolution 2.40Å

Drag the structure with the mouse to rotate

STRUCTURAL AND MECHANISTIC BASIS OF PENICILLIN BINDING PROTEIN INHIBITION BY LACTIVICINS

Overview

beta-lactam antibiotics, including penicillins and cephalosporins, inhibit, penicillin-binding proteins (PBPs), which are essential for bacterial cell, wall biogenesis. Pathogenic bacteria have evolved efficient antibiotic, resistance mechanisms that, in Gram-positive bacteria, include mutations, to PBPs that enable them to avoid beta-lactam inhibition. Lactivicin (LTV;, 1) contains separate cycloserine and gamma-lactone rings and is the only, known natural PBP inhibitor that does not contain a beta-lactam. Here we, show that LTV and a more potent analog, phenoxyacetyl-LTV (PLTV; 2), are, active against clinically isolated, penicillin-resistant Streptococcus, pneumoniae strains. Crystallographic analyses of S. pneumoniae PBP1b, reveal that LTV and PLTV inhibition involves opening of both monocyclic, cycloserine and gamma-lactone rings. In PBP1b complexes, the ring-derived, atoms from LTV and PLTV show a notable structural convergence with those, derived from a complexed cephalosporin (cefotaxime; 3). The structures, imply that derivatives of LTV will be useful in the search for new, antibiotics with activity against beta-lactam-resistant bacteria.

About this Structure

2JCH is a Single protein structure of sequence from Streptococcus pneumoniae r6 with SO4, CL, EDO and PL7 as ligands. Structure known Active Site: AC1. Full crystallographic information is available from OCA.

Reference

Structural and mechanistic basis of penicillin-binding protein inhibition by lactivicins., Macheboeuf P, Fischer DS, Brown T Jr, Zervosen A, Luxen A, Joris B, Dessen A, Schofield CJ, Nat Chem Biol. 2007 Aug 5;. PMID:17676039

Page seeded by OCA on Mon Nov 5 18:30:55 2007

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools