Structure and enzymatic mechanism of a moonlighting dUTPase
  • Metaadatok
Tartalom: http://journals.iucr.org/d/issues/2013/12/00/dw5050/index...
Archívum: MTA Könyvtár
Gyűjtemény: Status = Published


Type = Article
Cím:
Structure and enzymatic mechanism of a moonlighting dUTPase
Létrehozó:
Leveles, Ibolya
Németh, Veronika
Szabó E., Judit
Harmat, Veronika
Nyirí, Kinga
Bendes, Ábris
Papp-Kádár, Veronika
Zagyva, Imre
Róna, Gergely
Ozohanics, Olivér
Vékey, Károly
Tóth, Judit
Vértessy G., Beáta
Dátum:
2013
Téma:
QD04 Organic chemistry / szerves kémia
QD05 Crystallography / kristálytan
Tartalmi leírás:
Genome integrity requires well controlled cellular pools of nucleotides. dUTPases are responsible for regulating cellular dUTP levels and providing dUMP for dTTP biosynthesis. In Staphylococcus, phage dUTPases are also suggested to be involved in a moonlighting function regulating the expression of pathogenicity-island genes. Staphylococcal phage trimeric dUTPase sequences include a specific insertion that is not found in other organisms. Here, a 2.1 Ĺ resolution three-dimensional structure of a [varphi]11 phage dUTPase trimer with complete localization of the phage-specific insert, which folds into a small [beta]-pleated mini-domain reaching out from the dUTPase core surface, is presented. The insert mini-domains jointly coordinate a single Mg2+ ion per trimer at the entrance to the threefold inner channel. Structural results provide an explanation for the role of Asp95, which is suggested to have functional significance in the moonlighting activity, as the metal-ion-coordinating moiety potentially involved in correct positioning of the insert. Enzyme-kinetics studies of wild-type and mutant constructs show that the insert has no major role in dUTP binding or cleavage and provide a description of the elementary steps (fast binding of substrate and release of products). In conclusion, the structural and kinetic data allow insights into both the phage-specific characteristics and the generally conserved traits of [varphi]11 phage dUTPase.
Típus:
Article
PeerReviewed
info:eu-repo/semantics/article
Formátum:
text
Azonosító:
Leveles, Ibolya and Németh, Veronika and Szabó E., Judit and Harmat, Veronika and Nyirí, Kinga and Bendes, Ábris and Papp-Kádár, Veronika and Zagyva, Imre and Róna, Gergely and Ozohanics, Olivér and Vékey, Károly and Tóth, Judit and Vértessy G., Beáta (2013) Structure and enzymatic mechanism of a moonlighting dUTPase. Acta Crystallographica Section D: Biological Crystallography, D69. pp. 2298-2308. ISSN 1399-0047
Kapcsolat:
FP7 Biostruct-X project (contract No. 283570)