1llb
From Proteopedia
Line 1: | Line 1: | ||
[[Image:1llb.gif|left|200px]] | [[Image:1llb.gif|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_1llb", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | + | or leave the SCENE parameter empty for the default display. | |
- | | | + | --> |
- | | | + | {{STRUCTURE_1llb| PDB=1llb | SCENE= }} |
- | + | ||
- | + | ||
- | }} | + | |
'''Crystal Structure Of AmpC beta-Lactamase From E. Coli In Complex With ATMO-penicillin''' | '''Crystal Structure Of AmpC beta-Lactamase From E. Coli In Complex With ATMO-penicillin''' | ||
Line 30: | Line 27: | ||
[[Category: Shoichet, B K.]] | [[Category: Shoichet, B K.]] | ||
[[Category: Trehan, I.]] | [[Category: Trehan, I.]] | ||
- | [[Category: | + | [[Category: Beta-lactamase]] |
- | [[Category: | + | [[Category: Cephalosporinase]] |
- | [[Category: | + | [[Category: Hydrolase]] |
- | [[Category: | + | [[Category: Serine]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 00:02:04 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 21:02, 2 May 2008
Crystal Structure Of AmpC beta-Lactamase From E. Coli In Complex With ATMO-penicillin
Overview
beta-lactamases confer resistance to beta-lactam antibiotics such as penicillins and cephalosporins. However, beta-lactams that form an acyl-intermediate with the enzyme but subsequently are hindered from forming a catalytically competent conformation seem to be inhibitors of beta-lactamases. This inhibition may be imparted by specific groups on the ubiquitous R(1) side chain of beta-lactams, such as the 2-amino-4-thiazolyl methoxyimino (ATMO) group common among third-generation cephalosporins. Using steric hindrance of deacylation as a design guide, penicillin and carbacephem substrates were converted into effective beta-lactamase inhibitors and antiresistance antibiotics. To investigate the structural bases of inhibition, the crystal structures of the acyl-adducts of the penicillin substrate amoxicillin and the new analogous inhibitor ATMO-penicillin were determined. ATMO-penicillin binds in a catalytically incompetent conformation resembling that adopted by third-generation cephalosporins, demonstrating the transferability of such sterically hindered groups in inhibitor design.
About this Structure
1LLB is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.
Reference
Using steric hindrance to design new inhibitors of class C beta-lactamases., Trehan I, Morandi F, Blaszczak LC, Shoichet BK, Chem Biol. 2002 Sep;9(9):971-80. PMID:12323371 Page seeded by OCA on Sat May 3 00:02:04 2008