Literature DB >> 3485771

Tertiary structural similarity between a class A beta-lactamase and a penicillin-sensitive D-alanyl carboxypeptidase-transpeptidase.

B Samraoui, B J Sutton, R J Todd, P J Artymiuk, S G Waley, D C Phillips.   

Abstract

beta-Lactam antibiotics--the penicillins, cephalosporins and related compounds--act by inhibiting enzymes that catalyse the final stages of the synthesis of bacterial cell walls. Recent crystallographic studies of representative enzymes are beginning to reveal the structural bases of antibiotic specificity and mechanism of action, while intensive efforts are being made to understand the beta-lactamase enzymes that are largely responsible for bacterial resistance to these antibiotics. It has been suggested that the beta-lactamases and beta-lactam target enzymes may be evolutionarily related and some similarity of amino-acid sequence around a common active-site serine residue supports this idea. We present here the first evidence from a comparison of three-dimensional structures in support of this hypothesis: the structure of beta-lactamase I from Bacillus cereus is similar to that of the penicillin-sensitive D-alanyl-D-alanine carboxypeptidase-transpeptidase from Streptomyces R61.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3485771     DOI: 10.1038/320378a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  32 in total

1.  Induction of a Streptomyces cacaoi beta-lactamase gene cloned in S. lividans.

Authors:  V M Lenzini; J Magdalena; C Fraipont; B Joris; A Matagne; J Dusart
Journal:  Mol Gen Genet       Date:  1992-10

2.  Site-directed mutagenesis and substrate-induced inactivation of beta-lactamase I.

Authors:  S J Thornewell; S G Waley
Journal:  Biochem J       Date:  1992-12-15       Impact factor: 3.857

3.  Importance of the two tryptophan residues in the Streptomyces R61 exocellular DD-peptidase.

Authors:  C Bourguignon-Bellefroid; J M Wilkin; B Joris; R T Aplin; C Houssier; F G Prendergast; J Van Beeumen; J M Ghuysen; J M Frère
Journal:  Biochem J       Date:  1992-03-01       Impact factor: 3.857

4.  OHIO-1 beta-lactamase is part of the SHV-1 family.

Authors:  D M Shlaes; C Currie-McCumber; A Hull; I Behlau; M Kron
Journal:  Antimicrob Agents Chemother       Date:  1990-08       Impact factor: 5.191

5.  The active sites of the beta-lactamases of Streptomyces cacaoi and Streptomyces albus G.

Authors:  F De Meester; B Joris; M V Lenzini; P Dehottay; T Erpicium; J Dusart; D Klein; J M Ghuysen; J M Frère; J Van Beeumen
Journal:  Biochem J       Date:  1987-06-01       Impact factor: 3.857

6.  Identification of amino acid substitutions that alter the substrate specificity of TEM-1 beta-lactamase.

Authors:  T Palzkill; D Botstein
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

7.  Visualization of penicillin-binding proteins during sporulation of Streptomyces griseus.

Authors:  J Hao; K E Kendrick
Journal:  J Bacteriol       Date:  1998-04       Impact factor: 3.490

8.  Beta-lactamases as fully efficient enzymes. Determination of all the rate constants in the acyl-enzyme mechanism.

Authors:  H Christensen; M T Martin; S G Waley
Journal:  Biochem J       Date:  1990-03-15       Impact factor: 3.857

9.  Imipenem as substrate and inhibitor of beta-lactamases.

Authors:  J Monks; S G Waley
Journal:  Biochem J       Date:  1988-07-15       Impact factor: 3.857

10.  The mechanism of action of DD-peptidases: the role of tyrosine-159 in the Streptomyces R61 DD-peptidase.

Authors:  J M Wilkin; M Jamin; C Damblon; G H Zhao; B Joris; C Duez; J M Frère
Journal:  Biochem J       Date:  1993-04-15       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.