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PDBsum entry 1nwc
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Oxidoreductase
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PDB id
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1nwc
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Contents |
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* Residue conservation analysis
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References listed in PDB file
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Key reference
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Title
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Capture of an intermediate in the catalytic cycle of l-Aspartate-Beta-Semialdehyde dehydrogenase.
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Authors
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J.Blanco,
R.A.Moore,
R.E.Viola.
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Ref.
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Proc Natl Acad Sci U S A, 2003,
100,
12613-12617.
[DOI no: ]
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PubMed id
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Abstract
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The structural analysis of an enzymatic reaction intermediate affords a unique
opportunity to study a catalytic mechanism in extraordinary detail. Here we
present the structure of a tetrahedral intermediate in the catalytic cycle of
aspartate-beta-semialdehyde dehydrogenase (ASADH) from Haemophilus influenzae at
2.0-A resolution. ASADH is not found in humans, yet its catalytic activity is
required for the biosynthesis of essential amino acids in plants and
microorganisms. Diaminopimelic acid, also formed by this enzymatic pathway, is
an integral component of bacterial cell walls, thus making ASADH an attractive
target for the development of new antibiotics. This enzyme is able to capture
the substrates aspartate-beta-semialdehyde and phosphate as an active complex
that does not complete the catalytic cycle in the absence of NADP. A distinctive
binding pocket in which the hemithioacetal oxygen of the bound substrate is
stabilized by interaction with a backbone amide group dictates the R
stereochemistry of the tetrahedral intermediate. This pocket, reminiscent of the
oxyanion hole found in serine proteases, is completed through hydrogen bonding
to the bound phosphate substrate.
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Figure 4.
Fig. 4. Schematic representation of the ASADH active site
with a bound hemithioacetal reaction intermediate. Interactions
between ASA and phosphate and key active site residues are shown.
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Figure 6.
Fig. 6. Proposed mechanism for the catalytic cycle of ASADH
shown in reverse biological direction. (A) Tetrahedral
intermediate derived from reaction with ASA. (B) Proposed acyl
intermediate with trigonal planar geometry. (C) Second
tetrahedral intermediate with covalently bound aspartyl
phosphate.
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