TY - JOUR
T1 - Catalytic mechanism and structure of viral flavin-dependent thymidylate synthase ThyX
AU - Graziani, Sébastien
AU - Bernauer, Julie
AU - Skouloubris, Stéphane
AU - Graille, Marc
AU - Zhou, Cong Zhao
AU - Marchand, Christophe
AU - Decottignies, Paulette
AU - Van Tilbeurgh, Herman
AU - Myllykallio, Hannu
AU - Liebl, Ursula
PY - 2006/8/18
Y1 - 2006/8/18
N2 - By using biochemical and structural analyses, we have investigated the catalytic mechanism of the recently discovered flavin-dependent thymidylate synthase ThyX from Paramecium bursaria chlorella virus-1 (PBCV-1). Site-directed mutagenesis experiments have identified several residues implicated in either NADPH oxidation or deprotonation activity of PBCV-1 ThyX. Chemical modification by diethyl pyrocarbonate and mass spectroscopic analyses identified a histidine residue (His53) crucial for NADPH oxidation and located in the vicinity of the redox active N-5 atom of the FAD ring system. Moreover, we observed that the conformation of active site key residues of PBCV-1 ThyX differs from earlier reported ThyX structures, suggesting structural changes during catalysis. Steady-state kinetic analyses support a reaction mechanism where ThyX catalysis proceeds via formation of distinct ternary complexes without formation of a methyl enzyme intermediate.
AB - By using biochemical and structural analyses, we have investigated the catalytic mechanism of the recently discovered flavin-dependent thymidylate synthase ThyX from Paramecium bursaria chlorella virus-1 (PBCV-1). Site-directed mutagenesis experiments have identified several residues implicated in either NADPH oxidation or deprotonation activity of PBCV-1 ThyX. Chemical modification by diethyl pyrocarbonate and mass spectroscopic analyses identified a histidine residue (His53) crucial for NADPH oxidation and located in the vicinity of the redox active N-5 atom of the FAD ring system. Moreover, we observed that the conformation of active site key residues of PBCV-1 ThyX differs from earlier reported ThyX structures, suggesting structural changes during catalysis. Steady-state kinetic analyses support a reaction mechanism where ThyX catalysis proceeds via formation of distinct ternary complexes without formation of a methyl enzyme intermediate.
U2 - 10.1074/jbc.M600745200
DO - 10.1074/jbc.M600745200
M3 - Article
C2 - 16707489
AN - SCOPUS:33747674260
SN - 0021-9258
VL - 281
SP - 24048
EP - 24057
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 33
ER -