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2AMJ

Crystal Structure of Modulator of Drug Activity B from Escherichia coli O157:H7

Summary for 2AMJ
Entry DOI10.2210/pdb2amj/pdb
Related2B3D
DescriptorModulator of drug activity B (2 entities in total)
Functional Keywordsoxidoreductase, menadione, dt-diaphorase, montreal-kingston bacterial structural genomics initiative, bsgi, structural genomics
Biological sourceEscherichia coli
Total number of polymer chains4
Total formula weight93801.46
Authors
Adams, M.A.,Jia, Z.,Montreal-Kingston Bacterial Structural Genomics Initiative (BSGI) (deposition date: 2005-08-09, release date: 2006-07-18, Last modification date: 2024-11-13)
Primary citationAdams, M.A.,Jia, Z.
Modulator of drug activity B from Escherichia coli: crystal structure of a prokaryotic homologue of DT-diaphorase.
J.Mol.Biol., 359:455-465, 2006
Cited by
PubMed Abstract: Modulator of drug activity B (MdaB) is a putative member of the DT-diaphorase family of NAD(P)H:oxidoreductases that afford cellular protection against quinonoid compounds. While there have been extensive investigations of mammalian homologues, putative prokaryotic members of this enzyme family have received little attention. The three-dimensional crystal structure of apo-MdaB reported herein exhibits significant structural similarity to a number of flavoproteins, including the mammalian DT-diaphorases. We have shown by mass spectrometry that the endogenously associated cofactor is flavin adenine dinucleotide and we present here the structure of MdaB in complex with this compound. Growth of Escherichia coli carrying null mutations in the genes encoding MdaB or quinol monooxygenase, the gene for which shares the mdaB promoter, were not affected by the presence of menadione. However, over-expression of recombinant quinol monooxygenase conferred a state of resistance against both tetracycline and adriamycin. This work suggests that the redox cycle formed by these proteins protects E. coli from the toxic effects of polyketide compounds rather than the oxidative stress of menadione alone.
PubMed: 16630630
DOI: 10.1016/j.jmb.2006.03.053
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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数据于2025-06-25公开中

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