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The 2.2 A structure of the rRNA methyltransferase ErmC' and its complexes with cofactor and cofactor analogs: implications for the reaction mechanism.
Schluckebier, G; Zhong, P; Stewart, K D; Kavanaugh, T J; Abad-Zapatero, C.
Afiliación
  • Schluckebier G; Abbott Laboratories, D46Y-AP 10, 100 Abbott Park Road, Abbott Park, IL, 60064, USA. gerd.schluckebier@abbott.com
J Mol Biol ; 289(2): 277-91, 1999 Jun 04.
Article en En | MEDLINE | ID: mdl-10366505
The rRNA methyltransferase ErmC' transfers methyl groups from S -adenosyl-l-methionine to atom N6 of an adenine base within the peptidyltransferase loop of 23 S rRNA, thus conferring antibiotic resistance against a number of macrolide antibiotics. The crystal structures of ErmC' and of its complexes with the cofactor S -adenosyl-l-methionine, the reaction product S-adenosyl-l-homocysteine and the methyltransferase inhibitor Sinefungin, respectively, show that the enzyme undergoes small conformational changes upon ligand binding. Overall, the ligand molecules bind to the protein in a similar mode as observed for other methyltransferases. Small differences between the binding of the amino acid parts of the different ligands are correlated with differences in their chemical structure. A model for the transition-state based on the atomic details of the active site is consistent with a one-step methyl-transfer mechanism and might serve as a first step towards the design of potent Erm inhibitors.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metiltransferasas Idioma: En Revista: J Mol Biol Año: 1999 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Países Bajos
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metiltransferasas Idioma: En Revista: J Mol Biol Año: 1999 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Países Bajos