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Title: Enzymatic and structural analysis of inhibitors designed against Mycobacterium tuberculosis thymidylate kinase - New insights into the phosphoryl transfer mechanism
Authors: Haouz, A ×
Vanheusden, V
Munier-Lehmann, H
Froeyen, Mathy
Herdewijn, Piet
Van Calenbergh, S
Delarue, M #
Issue Date: 2003
Publisher: Amer soc biochemistry molecular biology inc
Series Title: Journal of Biological Chemistry vol:278 issue:7 pages:4963-4971
Abstract: The chemical synthesis of new compounds designed as inhibitors of Mycobacterium tuberculosis TMP kinase (TMPK) is reported. The synthesis concerns TMP analogues modified at the 5-position of the thymine ring as well as a novel compound with a six-membered sugar ring. The binding properties of the analogues are compared with the known inhibitor azido-TMP, which is postulated here to work by excluding the TMP-bound Mg2+ ion. The crystallographic structure of the complex of one of the compounds, 5-CH2OH-dUMP, with TMPK has been determined at 2.0 Angstrom. It reveals a major conformation for the hydroxyl group in contact with a water molecule and a minor conformation pointing toward Ser(99). Looking for a role for Ser(99), we have identified an unusual catalytic triad, or a proton wire, made of strictly conserved residues (including Glu(6), Ser(99), Arg, and Asp(9)) that probably serves to protonate the transferred PO3 group. The crystallographic structure of the commercially available bisubstrate analogue P-1-(adenosine-5')-P-5-(thymidine-5')-pentaphosphate bound to TMPK is also reported at 2.45 Angstrom and reveals an alternative binding pocket for the adenine moiety of the molecule compared with what is observed either in the Escherichia coli or in the yeast enzyme structures. This alternative binding pocket opens a way for the design of a new family of specific inhibitors.
URI: 
ISSN: 0021-9258
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Medicinal Chemistry (Rega Institute)
× corresponding author
# (joint) last author

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