Literature DB >> 17768344

Crystallization and preliminary X-ray characterization of the Bacillus amyloliquefaciens YwrO enzyme.

Majed M AbuKhader1, John Heap, Cristina I De Matteis, Stephen W Doughty, Nigel Minton, Max Paoli.   

Abstract

CB1954 is an anticancer prodrug that is currently in clinical trials coupled with the Escherichia coli flavoenzyme nitroreductase (NTR) for use in directed-enzyme prodrug therapy (DEPT). The NTR enzyme is responsible for the conversion of the prodrug into a cytotoxic agent. The bifunctional alkylating agent produced by this bioactivation process leads to DNA damage and death of cancer cells. Recently, a novel flavoenzyme from Bacillus amyloliquefaciens, YwrO (Bam YwrO), was reported to be able to reduce CB1954 from its noncytotoxic form into its active form. The crystallization and preliminary X-ray diffraction analysis of two crystal forms of Bam YwrO are reported. The first crystal form is orthorhombic, with space group P22(1)2(1), and diffracts X-rays to 2.18 A resolution. The second crystal form is tetragonal, with space group P4(1), and diffracts X-rays to 3.4 A. Determination of the Bam YwrO crystal structure will provide an understanding of the molecular recognition between this enzyme and the anticancer prodrug CB1954.

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Year:  2007        PMID: 17768344      PMCID: PMC2376317          DOI: 10.1107/S1744309107035816

Source DB:  PubMed          Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun        ISSN: 1744-3091


  22 in total

Review 1.  Antibody directed enzyme prodrug therapy (ADEPT): a review of the experimental and clinical considerations.

Authors:  K N Syrigos; A A Epenetos
Journal:  Anticancer Res       Date:  1999 Jan-Feb       Impact factor: 2.480

2.  Likelihood-enhanced fast rotation functions.

Authors:  Laurent C Storoni; Airlie J McCoy; Randy J Read
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-02-25

3.  Crystal structure of human quinone reductase type 2, a metalloflavoprotein.

Authors:  C E Foster; M A Bianchet; P Talalay; Q Zhao; L M Amzel
Journal:  Biochemistry       Date:  1999-08-03       Impact factor: 3.162

4.  Bioactivation of 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB 1954) by human NAD(P)H quinone oxidoreductase 2: a novel co-substrate-mediated antitumor prodrug therapy.

Authors:  R J Knox; T C Jenkins; S M Hobbs; S Chen; R G Melton; P J Burke
Journal:  Cancer Res       Date:  2000-08-01       Impact factor: 12.701

Review 5.  From bench to bedside for gene-directed enzyme prodrug therapy of cancer.

Authors:  Gabi U Dachs; Joanna Tupper; Gillian M Tozer
Journal:  Anticancer Drugs       Date:  2005-04       Impact factor: 2.248

6.  The bioactivation of 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954)--II. A comparison of an Escherichia coli nitroreductase and Walker DT diaphorase.

Authors:  R J Knox; F Friedlos; R F Sherwood; R G Melton; G M Anlezark
Journal:  Biochem Pharmacol       Date:  1992-12-15       Impact factor: 5.858

7.  CB 1954 revisited. I. Disposition kinetics and metabolism.

Authors:  P Workman; R A White; K Talbot
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

Review 8.  Clostridia in cancer therapy.

Authors:  Nigel P Minton
Journal:  Nat Rev Microbiol       Date:  2003-12       Impact factor: 60.633

Review 9.  CB 1954: from the Walker tumor to NQO2 and VDEPT.

Authors:  Richard J Knox; Philip J Burke; Shiuan Chen; David J Kerr
Journal:  Curr Pharm Des       Date:  2003       Impact factor: 3.116

10.  Catalytic properties of NAD(P)H:quinone acceptor oxidoreductase: study involving mouse, rat, human, and mouse-rat chimeric enzymes.

Authors:  S Chen; R Knox; A D Lewis; F Friedlos; P Workman; P S Deng; M Fung; D Ebenstein; K Wu; T M Tsai
Journal:  Mol Pharmacol       Date:  1995-05       Impact factor: 4.436

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