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PDBsum entry 3f6b
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References listed in PDB file
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Key reference
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Title
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Detection and time course of formation of major thiamin diphosphate-Bound covalent intermediates derived from a chromophoric substrate analogue on benzoylformate decarboxylase.
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Authors
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S.Chakraborty,
N.S.Nemeria,
A.Balakrishnan,
G.S.Brandt,
M.M.Kneen,
A.Yep,
M.J.Mcleish,
G.L.Kenyon,
G.A.Petsko,
D.Ringe,
F.Jordan.
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Ref.
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Biochemistry, 2009,
48,
981-994.
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PubMed id
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Note: In the PDB file this reference is
annotated as "TO BE PUBLISHED". The citation details given above have
been manually determined.
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Abstract
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The mechanism of the enzyme benzoylformate decarboxylase (BFDC), which carries
out a typical thiamin diphosphate (ThDP)-dependent nonoxidative decarboxylation
reaction, was studied with the chromophoric alternate substrate
(E)-2-oxo-4(pyridin-3-yl)-3-butenoic acid (3-PKB). Addition of 3-PKB resulted in
the appearance of two transient intermediates formed consecutively, the first
one to be formed a predecarboxylation ThDP-bound intermediate with lambda(max)
at 477 nm, and the second one corresponding to the first postdecarboxylation
intermediate the enamine with lambda(max) at 437 nm. The time course of
formation/depletion of the PKB-ThDP covalent complex and of the enamine showed
that decarboxylation was slower than formation of the PKB-ThDP covalent adduct.
When the product of decarboxylation 3-(pyridin-3-yl)acrylaldehyde (PAA) was
added to BFDC, again an absorbance with lambda(max) at 473 nm was formed,
corresponding to the tetrahedral adduct of PAA with ThDP. Addition of
well-formed crystals of BFDC to a solution of PAA resulted in a high resolution
(1.34 A) structure of the BFDC-bound adduct of ThDP with PAA confirming the
tetrahedral nature at the C2alpha atom, rather than of the enamine, and
supporting the assignment of the lambda(max) at 473 nm to the PAA-ThDP adduct.
The structure of the PAA-ThDP covalent complex is the first example of a
product-ThDP adduct on BFDC. Similar studies with 3-PKB indicated that
decarboxylation had taken place. Evidence was also obtained for the slow
formation of the enamine intermediate when BFDC was incubated with benzaldehyde,
the product of the decarboxylation reaction thus confirming its presence on the
reaction pathway.
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