2i72

From Proteopedia

Revision as of 09:56, 23 January 2008 by OCA (Talk | contribs)
Jump to: navigation, search

2i72, resolution 2.200Å

Drag the structure with the mouse to rotate

AmpC beta-lactamase in complex with 5-diformylaminomethyl-benzo[b]thiophen-2-boronic acid

Overview

Benzo[b]thiophene-2-ylboronic acid, 1, is a 27 nM inhibitor of the class C, beta-lactamase AmpC and potentiates the activity of beta-lactam, antibiotics in bacteria that express this and related enzymes. As is often, true, the potency of compound 1 against the enzymes is much attenuated in, cell culture against Gram negative bacteria, where the minimum inhibitor, concentration of compound 1 is in the mid-micromolar range. Here, we, modulated the properties of this lead to enhance its ability to cross the, membrane, using a combination of X-ray crystallography, structure-based, design, and application of physical models of outer membrane crossing., This strategy led us to derivatives with substantially improved, permeability. Also, the greater solubility of these compounds allowed us, to measure their efficacy at higher concentrations than with the lead 1, leading to higher maximum potentiation of the antibiotic effect of, ceftazidime on resistant bacteria.

About this Structure

2I72 is a Single protein structure of sequence from Escherichia coli with as ligand. Active as Beta-lactamase, with EC number 3.5.2.6 Full crystallographic information is available from OCA.

Reference

Optimizing Cell Permeation of an Antibiotic Resistance Inhibitor for Improved Efficacy., Venturelli A, Tondi D, Cancian L, Morandi F, Cannazza G, Segatore B, Prati F, Amicosante G, Shoichet BK, Costi MP, J Med Chem. 2007 Nov 15;50(23):5644-5654. Epub 2007 Oct 23. PMID:17956081

Page seeded by OCA on Wed Jan 23 11:56:38 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools