1b12

From Proteopedia

Revision as of 08:04, 20 March 2008 by OCA (Talk | contribs)
Jump to: navigation, search


PDB ID 1b12

Drag the structure with the mouse to rotate
, resolution 1.95Å
Ligands: and
Gene: LEPB (Escherichia coli)
Activity: Hydrolase, with EC number 3.9.21.89
Coordinates: save as pdb, mmCIF, xml



CRYSTAL STRUCTURE OF TYPE 1 SIGNAL PEPTIDASE FROM ESCHERICHIA COLI IN COMPLEX WITH A BETA-LACTAM INHIBITOR


Overview

The signal peptidase (SPase) from Escherichia coli is a membrane-bound endopeptidase with two amino-terminal transmembrane segments and a carboxy-terminal catalytic region which resides in the periplasmic space. SPase functions to release proteins that have been translocated into the inner membrane from the cell interior, by cleaving off their signal peptides. We report here the X-ray crystal structure of a catalytically active soluble fragment of E. coli SPase (SPase delta2-75). We have determined this structure at 1.9 A resolution in a complex with an inhibitor, a beta-lactam (5S,6S penem), which is covalently bound as an acyl-enzyme intermediate to the gamma-oxygen of a serine residue at position 90, demonstrating that this residue acts as the nucleophile in the hydrolytic mechanism of signal-peptide cleavage. The structure is consistent with the use by SPase of Lys 145 as a general base in the activation of the nucleophilic Ser90, explains the specificity requirement at the signal-peptide cleavage site, and reveals a large exposed hydrophobic surface which could be a site for an intimate association with the membrane. As enzymes that are essential for cell viability, bacterial SPases present a feasible antibacterial target: our determination of the SPase structure therefore provides a template for the rational design of antibiotic compounds.

About this Structure

1B12 is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

Crystal structure of a bacterial signal peptidase in complex with a beta-lactam inhibitor., Paetzel M, Dalbey RE, Strynadka NC, Nature. 1998 Nov 12;396(6707):186-90. PMID:9823901

Page seeded by OCA on Thu Mar 20 10:04:55 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools