4xjc

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dCTP deaminase-dUTPase from Bacillus haloduransdCTP deaminase-dUTPase from Bacillus halodurans

Structural highlights

4xjc is a 6 chain structure with sequence from Alkalihalobacillus halodurans C-125. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 2.35Å
Ligands:, ,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

DCDB_HALH5 Bifunctional enzyme that catalyzes both the deamination of dCTP to dUTP and the hydrolysis of dUTP to dUMP without releasing the toxic dUTP intermediate.[HAMAP-Rule:MF_00146][1]

Publication Abstract from PubMed

Analysis of the genome of Bacillus halodurans strain C125 indicated that two pathways leading from a cytosine deoxyribonucleotide to dUMP, used for dTMP synthesis, was encoded by the bacterium. The responsible genes, the comEB gene and the dcdB gene, encoding dCMP deaminase and the bifunctional dCTP deaminase:dUTPase (DCD:DUT) were both shown to be expressed in B. halodurans and both genes were subject to repression by the nucleosides, thymidine and deoxycytidine. The latter nucleoside presumably excerts its repression after deamination by cytidine deaminase. Both comEB and dcdB were cloned, overexpressed in E. coli and purified to homogeneity. The enzymes were both active and displayed the expected regulatory properties: activation by dCTP for dCMP deaminase and dTTP inhibition for both enzymes. Structurally, the B. halodurans enzyme resembled Mycobacterium tuberculosis enzyme the most. An investigation of sequenced genomes from other species of the genus Bacillus revealed that not only B. halodurans but also Bacillus pseudofirmus, Bacillus thuringiensis, Bacillus hemocellulosilyticus, Bacillus marmarensis, Bacillus cereus and Bacillus megaterium all encode both the dCMP deaminase and DCD:DUT enzymes. In addition, eight dcdB homologs were registered in entrez-NCBI from Bacillus species within the genus where the whole genome had not yet been sequenced.

Bacillus halodurans strain C125 encodes and synthesizes enzymes from both known pathways to form dUMP directly from cytosine deoxyribonucleotides.,Oehlenschlaeger CB, Lovgreen MN, Reinauer E, Lehtinen E, Pind ML, Harris P, Martinussen J, Willemoes M Appl Environ Microbiol. 2015 Mar 6. pii: AEM.00268-15. PMID:25746996[2]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Oehlenschlaeger CB, Lovgreen MN, Reinauer E, Lehtinen E, Pind ML, Harris P, Martinussen J, Willemoes M. Bacillus halodurans strain C125 encodes and synthesizes enzymes from both known pathways to form dUMP directly from cytosine deoxyribonucleotides. Appl Environ Microbiol. 2015 Mar 6. pii: AEM.00268-15. PMID:25746996 doi:http://dx.doi.org/10.1128/AEM.00268-15
  2. Oehlenschlaeger CB, Lovgreen MN, Reinauer E, Lehtinen E, Pind ML, Harris P, Martinussen J, Willemoes M. Bacillus halodurans strain C125 encodes and synthesizes enzymes from both known pathways to form dUMP directly from cytosine deoxyribonucleotides. Appl Environ Microbiol. 2015 Mar 6. pii: AEM.00268-15. PMID:25746996 doi:http://dx.doi.org/10.1128/AEM.00268-15

4xjc, resolution 2.35Å

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